Name: intracellular recording, sensory field mapping, and culturing identified neurons in the leech, hirudo medicinalis
Uploaded: 2013-11-04T21:00:00
Duration: 11 min 53 s
Description: Watch this Scientific Journal Video about Intracellular Recording, Sensory Field Mapping, and Culturing Identified Neurons in the Leech, Hirudo medicinalis at JoVE.com

1. Preparation of Electrodes and Saline Solution
<ol>
	<li>Prepare physiological saline and electrodes before the animal is dissected. Leech Ringer&#8217;s solution consists of the following: 115.3 mM NaCl, 1.8 mM CaCl2, 4.0 mM KCl, 10 mM Tris/maleic acid or HEPES. Adjust the pH to 7.4.</li>
	<li>Prepare a Ag-Cl wire by dipping a cleaned silver wire into a small amount of bleach for 20 min&#160;or until the wire has a smooth dark gray finish. Wash the wire with distilled water before using. Then place the wire into a micropipette holder that plugs into the amplifier. &#160;</li>
	<li>Prepare a sharp glass electrode of borosilicate glass using a pipette puller. The electrode resistance should be on the order of 20 M&#8486;.</li>
	<li>Backfill the pipette with 3 M potassium acetate solution and insert in into the micropipette holder.</li>
	<li>For an extracellular electrode prepare a sharp glass pipette as described above,&#160; break the tip back by rubbing another sharp pipette near the sharp edge. Then fire polish the tip so that it does not tear the connectives. Plastic extracellular electrodes will also work as long as there is good contact between the electrode and the nerve.</li>
	<li>Insert the extracellular recording electrode into a micropipette holder (with Ag-Cl wire) that is fitted with a rubber tube and syringe for suction. Use the syringe to draw saline into the electrode at least to the level of the silver wire.</li>
	<li>Set up the hardware (amplifier and stimulus isolator) and software recording parameters by following the manual for your specific signal recording unit. See Leksrisawat et al.22 to view details on equipment used in the experiments described below.&#160; &#160;</li>
</ol>
2. Ventral Ganglion Dissection
<ol>
	<li>Dissect the leech in a large silicone elastomer-lined dish with leech Ringer&#8217;s solution. If the animal is stretched longitudinally it will be easier to remove the ventral nerve cord (see Figure 1A).</li>
	<li>With #10 or #11 size scalpel, make a longitudinal incision with very shallow cuts in the ventral midline. About the middle 2/3rd of the ventral cut is shown in Figure 1B. Try not to cut through the black stocking (the ventral blood sinus) until the animal is fully opened and the blood sinus is stretched without kinks. This blood sinus runs the length of the animal along the ventral midline. The VNC is contained inside of this blood vessel.</li>
	<li>After the skin has been cut the full length of the animal use the fine iris scissors to nick the blood sinus (Figure 2). Slip one blade of the fine iris scissors under the sinus and slightly raise the blade to separate it from the nerve tissue. Cut the sinus the length of the VNC while avoiding the nerve roots, segmental nerves, or the connectives between ganglia.</li>
	<li>Next, remove part of the ventral nerve cord by cutting the roots distal to where the blood vessel joins the roots. Repeat this process for each ganglion along the length of the ventral nerve cord.</li>
	<li>Transfer a segment of one or two ganglia to a smaller Petri dish. The ganglia or the single ganglion needs to be pinned taut with some slack.</li>
	<li>Pin the connectives and the roots so the ganglion glial sheath is slightly stretched to prevent the neuron cell bodies from moving around when impaling through the glial sheath and into the neuron of interest. The pins should be placed through the black sinus for the roots and in the middle of the two connectives to minimize damage of the axons (Figure 3).</li>
	<li>Place the Petri dish with preparation under the microscope and secure it with wax at the bottom of the dish to prevent movement.</li>
	<li>Carefully focus the light beam using a mirror and light condenser to see the neurons as in Figure 4A (schematically shown in Figure 4B). Notice the two large Retzius cells in the center of the ganglion.</li>
	<li>To make an intracellular recording of the Rz, T, P, and N neurons, carefully place the tip of the electrode over the cell of interest and gently lower the tip until a dimple is seen in the glial sheath.</li>
	<li>Tap the electrode holder or manipulator (very carefully) so that the electrode tip &#8220;pops&#8221; into the cell of interest.</li>
	<li>Inject short pulses (30-40 msec) of positive current (1-10 nA) into the cell to evoke action potentials.</li>
</ol>
3. Culturing Neurons from the Ventral Ganglion Preparation
<ol>
	<li>Pin the ganglia ventral side up in a clean dish containing L-15 with fetal calf serum (FCS) (Figure 3). Pin the roots so that the ganglia are slightly stretched as done above for intracellular recordings. With fine scissors, nick the glial capsule at one end, slip one scissors blade under the capsule, then cut across the glial capsule as shown in Figure 5A.</li>
	<li>Add 100 &#181;l aliquot of Collagenase/Dispase to the dish and place on a shaker for 15 min. Examine cells by moving the culture media around the exposed cell bodies. Return the cells to the shaker for another 15 min or longer until the cells come out with minimal suction.</li>
	<li>Use a pipette attached to a syringe to gently extract cells from the ganglion. Fire polish the pipette tip so that it is slightly larger than the cell body diameter. For Rz cells in an adult leech, the diameter should be approximately 50 &#181;m.</li>
	<li>Prepare a variety of pipettes with different diameters without a filament as this decreases the chances of the cells sticking inside the pipette. Store the pipettes in a bottle containing 80% ethanol (EtOH) using a cotton ball at the bottom to protect the tips from chipping. Remember to wash the EtOH out of the pipette with medium before aspirating cells.</li>
	<li>After the enzyme treatment, wash out the enzyme-containing medium with L-15 (with FCS) 2x. Identify the cells of interest and gently draw them into the pipette by pulling the syringe (Figure 6A). Discharge the aspirated cells into another dish which contains L-15 (with FCS).</li>
	<li>Until now, all procedures were non-sterile. Perform the following steps in a sterile hood. Place 3-4 large drops of sterile L-15 (with FCS) in different locations inside a sterile Petri dish.</li>
	<li>Pipette the cells into one of the before-mentioned drops, blowing them around in the drop to wash them. Repeat this in series in 3 or 4 drops of medium.</li>
	<li>Place cells in a clean Petri dish filled with L-15 (with FCS).</li>
	<li>Incubate the cells for 1-24 hr at room temperature. Afterwards the clean cells can be plated. By leaving the cells for a few hours or overnight the extracellular matrix comes off easily. Plate the cells immediately to generate longer processes.</li>
	<li>Use sterile substrate to coat a microwell dish and allow it to dry completely (overnight) before culturing experiments.</li>
	<li>After the dish has been coated, wash the dish gently with sterile water and then with a small amount of the L-15 medium. Remember to use the L-15 solution without the FCS added to allow the cells to adhere to the dish. The medium can be gently changed to L-15 with FCS after the cells have adhered to the substrate. If the cells are to be used a few hours after plating, then switching the medium to L-15 with FCS is not necessary.</li>
	<li>Position the cells next to each other at the time of plating to induce rapid synaptogenesis (Figure 6B). After 24 hr measure physiological activity in pairings of neurons.</li>
	<li>Use intracellular electrophysiological techniques to record RP or synaptic responses in cultured pairs of cells (stimulate 1 neuron through an intracellular electrode and record responses from the paired cell using a 2nd intracellular electrode).</li>
</ol>
4. Ganglion-body Wall Preparation
<ol>
	<li>Pin the leech dorsal side down in an elastomer-lined dish as described above.</li>
	<li>Pin the skin to one side with roots on the other side of the severed ganglion (Figure 7A, magnified in Figure 7B) or make a window on the ventral aspect of the leech over a ganglion (Figure 7C) with all the roots to the body wall intact.</li>
	<li>After obtaining a stable intracellular recording in one of the sensory cells (T, P, N) use a small glass rod that has been fire polished to lightly touch the skin in the same segment. If the neuron being recorded from is an N cell then more pressure will need to be applied to the skin. In most cases, the N cell will only respond if the skin is pinched with tweezers. For this reason these cells should be tried last as one might damage the skin or displace the intracellular recoding by disturbing the preparation in such a manner.</li>
	<li>One should be able to quickly sketch the skin and ganglion with details sufficient enough that a map of where one touched can be used to determine the receptive field for a particular neuron. After recording from as many T and P cells as possible on both sides of a ganglion try the N cells.</li>
	<li>In order to examine if the sensory neurons have processes that travel through the connectives in a rostral or caudal manner and then out the roots in the adjoining segment to the skin, the connectives between ganglia can be cut and the receptive fields reexamined in regards to the spread of detection. Basically one is examining if there has been any loss in the receptive field.</li>
</ol>
5. Injecting Fluorescent Dyes
<ol>
	<li>Prepare a leech ganglion as described above.</li>
	<li>Fill a microelectrode with a solution of Lucifer yellow-CH (3.0%) and lithium chloride (300 mM).</li>
	<li>Impale one of the sensory cells or Rz cells on the ventral side of the ganglion as described above.</li>
	<li>Inject dye into the cell by passing negative current (3nA) through the electrode for 15 min. Set the pulse duration to 100 msec and the frequency to 2 Hz.</li>
	<li>Visualize the dye-filled neurons by exciting the dye with a mercury lamp and a FITC/GFP filter set.</li>
</ol>

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The authors have nothing to disclose.

The purpose of this set of experiments was 1) to teach and exhibit the fundamental principles of intracellular recordings from identifiable neurons and 2) to recognize the characteristic shapes of electrical signals that can arise from these particular neuronal types using adult leeches. There is a rich history of investigations using the leech for neurophysiological investigations and research is ongoing in addressing questions of neural circuitry and gene regulation during development as well as during synaptic repair and regeneration10. Neuromodulation, particularly through biogenic amine pathways, has also been a successful research direction in the leech. By adding dopamine and other pharmacological agents to the nervous system through the saline solution, it has been shown that dopamine modulates neural networks involved in decision-making23 and motor patterns for crawling behavior24,25. This experimental approach is a simple (and inexpensive) way to incorporate modulation into the teaching laboratory, and adjusting the ionic makeup of the saline solution is an effective way to teach the Nernst and Goldman-Hodgkin-Katz equations.
To be successful with the ganglion preparations it is important to have the ganglion taut prior to attempting to poke a soma with an intracellular electrode. Otherwise the soma will move when pushing down on the glial packet. In addition, when desheathing the ganglion for removing neurons for culture, avoid the region of interest when cutting across the ganglion so somas are not damaged as they are removed. Also, excessive incubation in the enzymes may result in the neurons being too fragile to be removed. It requires some trial and error to achieve an ideal incubation time because each batch of enzymes is slightly different in their actions.
Further investigation to optimize culture media could improve this technique. Various factors, such as the presence of insulin, sugars, or growth factors could be examined for longer maintenance of cultures. To determine if cells maintain their capacity to synthesize transmitters, such as serotonin synthesis in Rz cells, neutral red staining can be applied to label serotonergic processes. Also microglial invasion to injured and regenerating tissue can be quantified by nuclear stains days after an injury.
Although this preparation has many benefits to offer in examining regeneration and repair as well as neural circuitry, the pharmacological and molecular identification of the various receptor subtypes at synapses have not been fully characterized. An expressed sequence tag library is available26, and the medicinal leech genome is currently being assembled27, but the main limitation in leech compared to some model preparations is the ability to modify the genome for selective genes in specific cell types. In embryos this limitation has been addressed by injecting DNA or dsRNA to regulate gene expression28. The gene gun technique has recently been used to express invertebrate connexin (innexin) proteins in leech neurons. Expression of an innexin from Hirudo verbana (Hve-inx6) is sufficient for the formation of ectopic gap junctions in the medicinal leech29. The medicinal leech&#8212;or H. verbena as it were30 &#160;is sure to advance our understanding of the physiology and evolution of electrical synapses over the next few years.&#160;

The leech preparation is useful for investigating the function of identifiable (sensory, motor and inter-neurons within the animal&#39;s central nervous system (CNS). The useful property of leech neurons is that the shape of their action potentials and biophysical properties are characteristic for a given cell type (i.e. P, N, T, Rz). Moreover neurons can be removed from the animal and cultured in a suitable medium in which the cells maintain their electrical characteristics for as long as 45 days1,2.
A distinct advantage of the leech ganglion for learning how to make electrophysiological recordings is that cells are characteristically and reliably arranged in the ganglion in a pattern that allows identification of distinct cell types from ganglion to ganglion and from animal to animal. The unique location and morphology of neurons in leech ganglia were noted by Retzius as early as 18913. Knowledge of the identity and function of a neuron is advantageous for investigating neural circuits and for making experiments with a given cell type. Due to the relatively large somata of the neurons within a ganglion they are visible with a dissecting microscope, and the somata can be selectively impaled with microelectrodes for recording their electrical properties.
Dyes and large molecules can be injected into individual cells and channel properties studied by patch clamp. Ionic currents that give rise to the various shapes of the characteristic action potentials in various neurons have been identified4-7. From investigations in the pattern of innervation and branching of individual neurons within the CNS, the synaptic connections have been reproduced in culture with identified neurons2,8. Studies in the leech ganglia have provided insight into the development of functional circuits that can be measured with electrophysiology as well as with whole animal behavior studies. The leech CNS has also served as a valuable preparation for investigating mechanisms involved with neuronal repair and regeneration in the whole animal and in culture4-6,9-12.
In mammalian brains it is a daunting task to explain behavior in terms of the properties and connections of individual identified neurons. In principle one can hope that the study of less complex systems such as the leech could help to define basic mechanisms used in higher animals. The connections that are used which underlie a swim pattern13,14 and rhythmicity of the heart15 have been well characterized in the leech. The ability of some leech neurons to form both electrical and chemical communication is intriguing. Some connections are bidirectional while others are unidirectional chemically but bidirectional electrically7. Understanding the synaptic connections within the animal as well as recreating the same type of connections in a culture dish are powerful tools for investigating synaptogenesis16-18 as well as pharmacological profiling of synapses19. The intracellular recording and stimulation techniques described here provide a foundation for pharmacological assays and research in neuroethology and development.
In addition, the segmental ventral nerve cord can be dissected with a patch of innervated skin. With the ability to keep a patch of skin and the neurons alive, sensory receptive fields can be probed by recording electrical signals from the cell body (i.e. soma) of sensory neurons within respective abdominal ganglion in the CNS. Thereby one can assess the sensitivity of the sensory endings by applying varying degrees of force on the skin and map receptive fields: light touch, pressure, and noxious (painful) stimuli20,21.
An advantage of this leech ganglion-skin preparation is that one can draw anatomically the receptive field map and trace the neuronal processes to the identified neuron once the electrical responses are being recorded. The three leech experiments described below can all be completed multiple times with a single specimen, which makes this a cost effective teaching module for academic laboratories.

<table border="0" cellpadding="0" cellspacing="0" width="256">
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			<td height="22" style="height:22px;width:64px;">Sylgard</td>
			<td style="width:64px;">Dow Corning</td>
			<td style="width:64px;">&#160;182 silicone kit</td>
			<td style="width:64px;"></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">NaCl</td>
			<td>Sigma-Aldrich</td>
			<td>&#160;S7653</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">KCl</td>
			<td>Sigma-Aldrich</td>
			<td>&#160;P9333&#160;</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">CaCl2</td>
			<td>Sigma-Aldrich</td>
			<td>&#160;C5670&#160;</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Tris/maleic acid</td>
			<td>Sigma-Aldrich</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Bleach&#160;</td>
			<td>Sigma-Aldrich</td>
			<td></td>
			<td>To chloride silver wire</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">NaOH</td>
			<td>Sigma-Aldrich</td>
			<td>&#160;221465&#160;</td>
			<td>To adjust pH</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">HCl</td>
			<td>Sigma-Aldrich</td>
			<td>&#160;H1758</td>
			<td>To adjust pH</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;"></td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="21">
			<td colspan="3" height="21" style="height:21px;">CULTURING MATERIALS</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Name of the Reagent</td>
			<td>Company</td>
			<td>Catalogue Number</td>
			<td>Comments</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Collagenase/Dispase</td>
			<td>Boehringer Mannheim&#160;</td>
			<td>&#160;269-638</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Leibovitz L-15 with L-Glutamine</td>
			<td>Gibco</td>
			<td>041-01415H</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="43" rowspan="2" style="height:43px;">Fetal calf serum</td>
			<td>Ready Systems Ag&#160;</td>
			<td rowspan="2"></td>
			<td rowspan="2"></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">04-001</td>
		</tr>
		<tr height="102">
			<td height="102" style="height:102px;">D-Glucose-Monohydrate</td>
			<td>Merck</td>
			<td>8342</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Gentamycin sulfate&#160;</td>
			<td>any&#160; supplier</td>
			<td></td>
			<td>10 mg/ml</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Glutamine</td>
			<td>Gibco</td>
			<td>043-0503H</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">HEPES</td>
			<td>Sigma</td>
			<td>3375</td>
			<td>Free acid, crystalline</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Concanavalin A Type IV</td>
			<td>Sigma&#160;</td>
			<td>C 2010</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Poly-L-Lysine Hydrobromide</td>
			<td>Sigma&#160;</td>
			<td>P 7890</td>
			<td>MW 15-30,000</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">&#160;Microwell plate, 60 x 10 &#956;l</td>
			<td>Falcon</td>
			<td>3034</td>
			<td>Flat bottom, 10 in a bag</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;"></td>
			<td></td>
			<td></td>
			<td></td>
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		<tr height="22">
			<td height="22" style="height:22px;">Material Name</td>
			<td>Company</td>
			<td>Catalogue Number</td>
			<td>Comments</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Dissecting tools</td>
			<td>World Precision Instruments</td>
			<td>&#160;assortment</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Intracellular electrode probe</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Faraday cage</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Insect Pins</td>
			<td>Fine Science Tools, Inc</td>
			<td>&#160;26001-60</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Dissecting microscope (100X)</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Fiber optic lamp</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Small adjustable mirror</td>
			<td></td>
			<td></td>
			<td>To direct light beam toward the preparation.</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Glass electrodes</td>
			<td>Sigma-Aldrich</td>
			<td>&#160;CLS7095B5X</td>
			<td>Box of 200, Suction electrodes</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Micromanipulator</td>
			<td>World Precision Instruments</td>
			<td>&#160;MD4-M3-R</td>
			<td>&#160;Can fix for base or on a metal rod</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Raised preparation stand</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Silver wire (10/1,000 inch)</td>
			<td>A-M Systems</td>
			<td>&#160;782500</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Computer</td>
			<td>any company</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">AC/DC differential amplifier</td>
			<td>A-M Systems</td>
			<td>Model 3000</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">PowerLab 26T</td>
			<td>AD Instruments</td>
			<td>&#160;27T</td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Head stage</td>
			<td>AD Instruments</td>
			<td></td>
			<td>Comes with AC/DC amplifier</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">LabChart7</td>
			<td>AD Instruments</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Electrical leads</td>
			<td>any company</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Glass tools&#160;</td>
			<td>make yourself</td>
			<td></td>
			<td>For manipulating nerves</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Cable and connectors</td>
			<td>any company</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Pipettes with bulbs&#160;</td>
			<td>&#160;Fisher Scientific&#160;</td>
			<td>&#160;13-711-7</td>
			<td>Box of 500</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Beakers</td>
			<td>any company</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Wax or modeling clay</td>
			<td>any company or local stores</td>
			<td></td>
			<td></td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;">Stimulator</td>
			<td>Grass Instruments</td>
			<td>SD9 or S88</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="43" rowspan="2" style="height:43px;">Plastic tip for suction electrode</td>
			<td rowspan="2">local hardware store (Watt&#8217;s brand)</td>
			<td rowspan="2">&#188; inch OD x 0.170 inch ID</td>
			<td>Cut in small pieces. Pull out over a flame and cut back the tip to the correct size.</td>
		</tr>
		<tr height="22">
			<td height="22" style="height:22px;"></td>
		</tr>
	</tbody>
</table>

intracellular recording, sensory field mapping, and culturing identified neurons in the leech, hirudo medicinalis

The freshwater leech, Hirudo medicinalis, is a versatile model organism that has been used to address scientific questions in the fields of neurophysiology, neuroethology, and developmental biology. The goal of this report is to consolidate experimental techniques from the leech system into a single article that will be of use to physiologists with expertise in other nervous system preparations, or to biology students with little or no electrophysiology experience. We demonstrate how to dissect the leech for recording intracellularly from identified neural circuits in the ganglion. Next we show how individual cells of known function can be removed from the ganglion to be cultured in a Petri dish, and how to record from those neurons in culture. Then we demonstrate how to prepare a patch of innervated skin to be used for mapping sensory or motor fields. These leech preparations are still widely used to address basic electrical properties of neural networks, behavior, synaptogenesis, and development. They are also an appropriate training module for neuroscience or physiology teaching laboratories.

Intracellular recordings from sensory neurons in the leech ganglion are characterized by their distinct voltage-time traces shown in Figure 4C. The resting cell membrane potential in healthy leech ganglion cells is -45 to -60 mV. If potentials are smaller (less negative) one should change the glass electrode, or if the potential is still low, move on to another segment of the nerve cord. Spontaneous action potentials with small amplitude may indicate that the electrode is in a motor neuron. If this happens in the ganglion-body wall a current injection can be used to determine if the neuron innervates any of the muscles still attached to the skin. The annulus erector motor neuron (AE) is on the ventral side of the ganglion (Figure 4B) and it will cause the annuli (ridges or segments) to rise by activating the annulus erector muscle.
Injecting current into the sensory cells should evoke action potentials with the characteristic waveforms shown in Figure 4C. If the waveforms look different it could be due to an unbalanced bridge or offset capacitance compensation. One should consult the manual that accompanies the signal acquisition unit for details on how to balance the bridge inside a cell. Notice the stimulus artifacts at the beginning and end of the current pulses in Figure 4C. This is how the artifacts look when the bridge is balanced.
Primary cultures of neurons from the leech ganglion form electrical and chemical synapses in the dish. Initially the electrical properties of the cultured cells are not exactly the same as they are in vivo. However after a few days the impulses are nearly indistinguishable from those recorded in the ganglion. This is demonstrated in Figure 6C with a pair of Rz cells. After 7 hr in culture the amplitude of synaptic potentials was 1-2 mV. After 56 hr in culture synaptic potentials were larger than 10 mV (top traces in Figure 6C). The shape of the action potential also changes after 56hr in culture. Under the conditions described these cells are viable for several days.
Intercellular communication can be demonstrated by stimulating the nerve roots or connectives and recording from neurons in the ganglion. Stimulating these nerves generates robust synaptic potentials and action potentials in different ganglion cells. Traces in Figure 8B were recorded from a Retzius cell in a ganglion that had been removed from the animal and pinned out in a dish. The black trace was evoked by a subthreshold stimulus applied with an extracellular electrode to the connective. Increasing the stimulus voltage caused the cell to fire an action potential (red trace). Fluorescent dyes or horse radish peroxidase can be injected into these cells to study their morphology. Lucifer yellow was injected into an Rz neuron by passing a negative current through the electrode. An alternative is to inject the dye using puffs of air pressure. Figure 9A shows the dye shortly after the injection began. Thirty minutes later the dye already had diffused into the nerve roots (Figure 9B). The type of dye depends on the application, e.g. small molecular weight dyes that can pass through gap junctions are used to identify electrical synapses.
<img alt="Figure 1" fo:content-width="5in" src="/files/ftp_upload/50631/50631fig1.jpg" width="600px" /> 
Figure 1. Ventral leech dissection. (A) The animal is thoroughly pinned ventral side up in an elastomer-lined dish filled with leech saline. (B) A shallow incision spanning the anterior: posterior axis is made just lateral to the midline to avoid damaging the nerve cord. The black blood sinus (which contains the ventral nerve cord) can easily be seen. Note the one exposed ganglion that is white compared to the sheath. <a href="https://www.jove.com/files/ftp_upload/50631/50631fig1highres.jpg" target="_blank">Click here to view larger image</a>.
<img alt="Figure 2" fo:content-width="5in" src="/files/ftp_upload/50631/50631fig2.jpg" width="600px" /> 
Figure 2. Dissection of the black sinus. The blood vessel (arrow) should be carefully cut on one side to expose the ventral nerve cord (double arrow). Leave segments of the blood vessel intact around the segmental roots for use as a handle to manipulate the ventral nerve cord when transferring between dissection and recording dishes. <a href="https://www.jove.com/files/ftp_upload/50631/50631fig2highres.jpg" target="_blank">Click here to view larger image</a>.
<img alt="Figure 3" fo:content-width="3in" src="/files/ftp_upload/50631/50631fig3.jpg" width="400px" /> 
Figure 3. Isolated section of the ventral nerve cord. Pinning the ventral nerve cord by the blood vessel fragments remaining on the segmental roots and at the ends of the segmental connectives exposes the ganglia for electrophysiological recordings. A taut stretching of the ganglia allows one to see the identifiable cell bodies and will allow an easier penetration of the glial sheath with a sharp glass electrode. <a href="https://www.jove.com/files/ftp_upload/50631/50631fig3highres.jpg" target="_blank">Click here to view larger image</a>.
<img alt="Figure 4" fo:content-width="5in" src="/files/ftp_upload/50631/50631fig4.jpg" width="600px" /> 
Figure 4. Cellular anatomy of the leech ganglion. (A) Ideally the Retzius cells (R) and other large cell bodies (P- pressure, T- touch, N-nociceptive, AE- annulus erector) will be clearly visible if the microscope and light condenser are set up properly. (B) Schematic view of cells in the ganglion. Slight differences in the location of the somas will occur in each ganglion due to how the ganglion is stretched and pinned taut. (C) Action potentials recorded from the soma of these neurons have characteristic waveforms. These spikes were evoked by injecting positive current into the cell (square pulse overlaying the voltage-time traces). <a href="https://www.jove.com/files/ftp_upload/50631/50631fig4highres.jpg" target="_blank">Click here to view larger image</a>.
<img alt="Figure 5" fo:content-width="5in" src="/files/ftp_upload/50631/50631fig5.jpg" width="600px" /> 
Figure 5. Desheathing the ganglion to remove individual cell bodies. (A) The glial sheath should be carefully cut across the ganglion to avoid damaging cells of interest. The red line indicates a cut to avoid hitting the soma of the Rz neurons. Opening the sheath gives the digestive enzymes access to the connective tissue matrix. (B) Healthy cell bodies bulging out of the ganglion after the glial sheath has been opened. <a href="https://www.jove.com/files/ftp_upload/50631/50631fig5highres.jpg" target="_blank">Click here to view larger image</a>.
<img alt="Figure 6" fo:content-width="5in" src="/files/ftp_upload/50631/50631fig6.jpg" width="600px" /> 
Figure 6. Culturing neurons from the leech ganglion. (A) Cells are aspirated from the ganglion using a micropipette and transferred to a dish containing culture media. (B) Placing multiple cells near one another will increase the rate of synaptogenesis between identifiable neurons. Here the stumps of two neurons have formed a synapse. (C) Neurons in culture exhibit slightly different electrical properties. The top traces show synaptic potentials evoked by stimulating the adjacent cell 7 hr and 56 hr after the cells were plated. The bottom traces were evoked by injecting current directly into one of the Rz cells. Note the increase in synaptic potential amplitude and change in the action potential waveform after 56 hr in culture. <a href="https://www.jove.com/files/ftp_upload/50631/50631fig6highres.jpg" target="_blank">Click here to view larger image</a>.
<img alt="Figure 7" fo:content-width="5in" src="/files/ftp_upload/50631/50631fig7.jpg" width="600px" /> 
Figure 7. The leech ganglion-body wall preparation for mapping receptive fields. (A) One approach is to remove an entire section of the body wall along with 1-3 ganglia. Here the roots on one side have been cut and the ganglion has been pinned out to the side. (B) A pinned out ganglion at higher magnification. (C) Another approach is to create a small window in the body wall and record from the intact ganglia while mapping a receptive field. (D-G) Each of the sensory neurons exhibits a characteristic response to a mechanical stimulus. (D) A light touch evokes activity in T cells but not in P or N cells. (E) The T cell response shuts off in response to stronger stimuli, giving way to activation of the P cell. As the stimulus gets stronger the N cells becomes activated (F-G). <a href="https://www.jove.com/files/ftp_upload/50631/50631fig7highres.jpg" target="_blank">Click here to view larger image</a>.
<img alt="Figure 8" fo:content-width="5in" src="/files/ftp_upload/50631/50631fig8.jpg" width="600px" /> 
Figure 8. Evoked activity in the leech ganglion. Extracellular stimulation of the connectives can be used to drive synaptic transmission in the nerve cord. (A) This is done by attaching a suction electrode to one of the connectives and applying a small voltage. The sharp glass electrode (arrow) can be seen impaling a Retzius cell in the ganglion. (B) Voltage-time traces showing the stimulus artifact followed by a synaptic potential (black) and an action potential (red). <a href="https://www.jove.com/files/ftp_upload/50631/50631fig8highres.jpg" target="_blank">Click here to view larger image</a>.
<img alt="Figure 9" fo:content-width="5in" src="/files/ftp_upload/50631/50631fig9.jpg" width="600px" /> 
Figure 9. Injecting dye into leech neurons. (A) Lucifer yellow can be injected into the soma by passing current through the recording microelectrode. A mercury lamp and FITC filter set can then be used to visualize the fluorescence. (B) Dye has diffused into the Rz axons about 30 min&#160;after the injection. <a href="https://www.jove.com/files/ftp_upload/50631/50631fig9highres.jpg" target="_blank">Click here to view larger image</a>.

Watch this Scientific Journal Video about Intracellular Recording, Sensory Field Mapping, and Culturing Identified Neurons in the Leech, Hirudo medicinalis at JoVE.com

Intracellular Recording, Sensory Field Mapping, and Culturing Identified Neurons in the Leech, Hirudo medicinalis

This article describes three nervous system preparations using leeches: intracellular recording from neurons in ventral ganglia, culturing neurons from ventral ganglia, and recording from a patch of innervated skin to map sensory fields.

Intracellular Recording, Sensory Field Mapping, and Culturing Identified Neurons in the Leech, Hirudo medicinalis

The freshwater leech, Hirudo medicinalis, is a versatile model organism that has been used to address scientific questions in the fields of ...

intracellular-recording-sensory-field-mapping-culturing-identified

Research

JoVE Journal

Neuroscience

Analyzing Responses of Mouse Olfactory Sensory Neurons Using the Air-phase Electroolfactogram Recording

Animals depend on olfaction for many critical behaviors, such as finding food sources, avoiding predators, and identifying conspecifics for mating and other social interactions. The electroolfactogram (EOG) recording is an informative, easy to conduct, and reliable method to assay olfactory function at the level of the olfactory epithelium. Since the 1956 description of the EOG by Ottoson in frogs1, the EOG recording has been applied in many vertebrates including salamanders, rabbits, rats, mice, and humans (reviewed by Scott and Scott-Johnson, 2002, ref. 2). The recent advances in genetic modification in mice have rekindled interest in recording the EOG for physiological characterization of olfactory function in knock-out and knock-in mice. EOG recordings have been successfully applied to demonstrate the central role of olfactory signal transduction components3-8, and more recently to characterize the contribution of certain regulatory mechanisms to OSN responses9-12.
Odorant detection occurs at the surface of the olfactory epithelium on the cilia of OSNs, where a signal transduction cascade leads to opening of ion channels, generating a current that flows into the cilia and depolarizes the membrane13. The EOG is the negative potential recorded extracellularly at the surface of the olfactory epithelium upon odorant stimulation, resulting from a summation of the potential changes caused by individual responsive OSNs in the recording field2. Comparison of the amplitude and kinetics of the EOG thus provide valuable information about how genetic modification and other experimental manipulations influence the molecular signaling underlying the OSN response to odor. 
Here we describe an air-phase EOG recording on a preparation of mouse olfactory turbinates. Briefly, after sacrificing the mouse, the olfactory turbinates are exposed by bisecting the head along the midline and removing the septum. The turbinate preparation is then placed in the recording setup, and a recording electrode is placed at the surface of the olfactory epithelium on one of the medial turbinates. A reference electrode is electrically connected to the tissue through a buffer solution. A continuous stream of humidified air is blown over the surface of the epithelium to keep it moist. The vapor of odorant solutions is puffed into the stream of humidified air to stimulate the epithelium. Responses are recorded and digitized for further analysis.

The electroolfactogram (EOG) recording is an informative, easy-to-conduct, and reliable way of assessing olfactory function at the level of the olfactory epithelium. This protocol describes a recording setup, mouse tissue preparation, data collection, and basic data analysis.

Animals depend on olfaction for many critical behaviors, such as finding food sources, avoiding predators, and identifying conspecifics for mating and ...

Live-imaging of PKC Translocation in Sf9 Cells and in Aplysia Sensory Neurons

Protein kinase Cs (PKCs) are serine threonine kinases that play a central role in regulating a wide variety of cellular processes such as cell growth and learning and memory. There are four known families of PKC isoforms in vertebrates: classical PKCs (&alpha;, &beta;I, &beta;II and &gamma;), novel type I PKCs (&#949; and &eta;), novel type II PKCs (&delta; and &theta;), and atypical PKCs (&zeta; and &iota;). The classical PKCs are activated by Ca2+ and diacylclycerol (DAG), while the novel PKCs are activated by DAG, but are Ca2+-independent. The atypical PKCs are activated by neither Ca2+ nor DAG. In Aplysia californica, our model system to study memory formation, there are three nervous system specific PKC isoforms one from each major class, namely the conventional PKC Apl I, the novel type I PKC Apl II and the atypical PKC Apl III. PKCs are lipid-activated kinases and thus activation of classical and novel PKCs in response to extracellular signals has been frequently correlated with PKC translocation from the cytoplasm to the plasma membrane. Therefore, visualizing PKC translocation in real time in live cells has become an invaluable tool for elucidating the signal transduction pathways that lead to PKC activation. For instance, this technique has allowed for us to establish that different isoforms of PKC translocate under different conditions to mediate distinct types of synaptic plasticity and that serotonin (5HT) activation of PKC Apl II requires production of both DAG and phosphatidic acid (PA) for translocation 1-2. Importantly, the ability to visualize the same neuron repeatedly has allowed us, for example, to measure desensitization of the PKC response in exquisite detail 3. In this video, we demonstrate each step of preparing Sf9 cell cultures, cultures of Aplysia sensory neurons have been described in another video article 4, expressing fluorescently tagged PKCs in Sf9 cells and in Aplysia sensory neurons and live-imaging of PKC translocation in response to different activators using laser-scanning microscopy.

In this video, we demonstrate visualization of PKC translocation in living cells using fluorescently tagged PKCs.

Protein kinase Cs (PKCs) are serine threonine kinases that play a central role in regulating a wide variety of cellular processes such as cell growth and ...

Flash Photolysis of Caged Compounds in the Cilia of Olfactory Sensory  Neurons

Photolysis of caged compounds allows the production of rapid and localized increases in the concentration of various physiologically active compounds1. Caged compounds are molecules made physiologically inactive by a chemical cage that can be broken by a flash of ultraviolet light. Here, we show how to obtain patch-clamp recordings combined with photolysis of caged compounds for the study of olfactory transduction in dissociated mouse olfactory sensory neurons. The process of olfactory transduction (Figure 1) takes place in the cilia of olfactory sensory neurons, where odorant binding to receptors leads to the increase of cAMP that opens cyclic nucleotide-gated (CNG) channels2. Ca entry through CNG channels activates Ca-activated Cl channels. We show how to dissociate neurons from the mouse olfactory epithelium3 and how to activate CNG channels or Ca-activated Cl channels by photolysis of caged cAMP4 or caged Ca5. We use a flash lamp6,7 to apply ultraviolet flashes to the ciliary region to uncage cAMP or Ca while patch-clamp recordings are taken to measure the current in the whole-cell voltage-clamp configuration8-11.

Photolysis of caged compounds allows the production of rapid and localized increases in the concentration of various physiologically active compounds. Here, we show how to obtain patch-clamp recordings combined with photolysis of caged cAMP or caged Ca for the study of olfactory transduction in dissociated mouse olfactory sensory neurons.

Photolysis of caged compounds allows the production of rapid and localized increases in the concentration of various physiologically active compounds1. ...

Simultaneous Recording of Calcium Signals from Identified Neurons and Feeding Behavior of Drosophila melanogaster

To study neuronal networks in terms of their function in behavior, we must analyze how neurons operate when each behavioral pattern is generated. Thus, simultaneous recordings of neuronal activity and behavior are essential to correlate brain activity to behavior. For such behavioral analyses, the fruit fly, Drosophila melanogaster, allows us to incorporate genetically encoded calcium indicators such as GCaMP1, to monitor neuronal activity, and to use sophisticated genetic manipulations for optogenetic or thermogenetic techniques to specifically activate identified neurons2-5. Use of a thermogenetic technique has led us to find critical neurons for feeding behavior (Flood et al., under revision). As a main part of feeding behavior, a Drosophila adult extends its proboscis for feeding6 (proboscis extension response; PER), responding to a sweet stimulus from sensory cells on its proboscis or tarsi. Combining the protocol for PER7 with a calcium imaging technique8 using GCaMP3.01, 9, I have established an experimental system, where we can monitor activity of neurons in the feeding center &#x2013; the suboesophageal ganglion (SOG), simultaneously with behavioral observation of the proboscis. I have designed an apparatus ("Fly brain Live Imaging and Electrophysiology Stage": "FLIES") to accommodate a Drosophila adult, allowing its proboscis to freely move while its brain is exposed to the bath for Ca2+ imaging through a water immersion lens. The FLIES is also appropriate for many types of live experiments on fly brains such as electrophysiological recording or time lapse imaging of synaptic morphology. Because the results from live imaging can be directly correlated with the simultaneous PER behavior, this methodology can provide an excellent experimental system to study information processing of neuronal networks, and how this cellular activity is coupled to plastic processes and memory.

Simultaneous Recording of Calcium Signals from Identified Neurons and Feeding Behavior of Drosophila melanogaster

The fruit fly, Drosophila melanogaster, extends its proboscis for feeding, responding to a sugar stimulus from its proboscis or tarsus. I have combined observations of the proboscis extension response (PER) with a calcium imaging technique, allowing us to monitor the activity of neurons in the brain, simultaneously with behavioral observation.

To study neuronal networks in terms of their function in behavior, we must analyze how neurons operate when each behavioral pattern is generated.  Thus, ...

Retrograde Fluorescent Labeling Allows for Targeted Extracellular Single-unit Recording from Identified Neurons In vivo

The overall goal of this method is to record single-unit responses from an identified population of neurons. In vivo electrophysiological recordings from individual neurons are critical for understanding how neural circuits function under natural conditions. Traditionally, these recordings have been performed 'blind', meaning the identity of the recorded cell is unknown at the start of the recording. Cellular identity can be subsequently determined via intracellular1, juxtacellular2 or loose-patch3 iontophoresis of dye, but these recordings cannot be pre-targeted to specific neurons in regions with functionally heterogeneous cell types. Fluorescent proteins can be expressed in a cell-type specific manner permitting visually-guided single-cell electrophysiology4-6. However, there are many model systems for which these genetic tools are not available. Even in genetically accessible model systems, the desired promoter may be unknown or genetically homogenous neurons may have varying projection patterns. Similarly, viral vectors have been used to label specific subgroups of projection neurons7, but use of this method is limited by toxicity and lack of trans-synaptic specificity. Thus, additional techniques that offer specific pre-visualization to record from identified single neurons in vivo are needed. Pre-visualization of the target neuron is particularly useful for challenging recording conditions, for which classical single-cell recordings are often prohibitively difficult8-11. The novel technique described in this paper uses retrograde transport of a fluorescent dye applied using tungsten needles to rapidly and selectively label a specific subset of cells within a particular brain region based on their unique axonal projections, thereby providing a visual cue to obtain targeted electrophysiological recordings from identified neurons in an intact circuit within a vertebrate CNS.
The most significant novel advancement of our method is the use of fluorescent labeling to target specific cell types in a non-genetically accessible model system. Weakly electric fish are an excellent model system for studying neural circuits in awake, behaving animals12. We utilized this technique to study sensory processing by "small cells" in the anterior exterolateral nucleus (ELa) of weakly electric mormyrid fish. "Small cells" are hypothesized to be time comparator neurons important for detecting submillisecond differences in the arrival times of presynaptic spikes13. However, anatomical features such as dense myelin, engulfing synapses, and small cell bodies have made it extremely difficult to record from these cells using traditional methods11, 14. Here we demonstrate that our novel method selectively labels these cells in 28% of preparations, allowing for reliable, robust recordings and characterization of responses to electrosensory stimulation.

Retrograde Fluorescent Labeling Allows for Targeted Extracellular Single-unit Recording from Identified Neurons In vivo

Retrograde transport of fluorescent dye labels a sub-population of neurons based on anatomical projection. Labeled axons can be visually targeted in vivo, permitting extracellular recording from identified axons. This technique facilitates recording when neurons cannot be labeled through genetic manipulation or are difficult to isolate using 'blind' in vivo approaches.

The overall goal of this method is to record single-unit responses from an identified population of neurons. In vivo electrophysiological recordings from ...

Recording Electrical Activity from Identified Neurons in the Intact Brain of Transgenic Fish

Understanding the cell physiology of neural circuits that regulate complex behaviors is greatly enhanced by using model systems in which this work can be performed in an intact brain preparation where the neural circuitry of the CNS remains intact. We use transgenic fish in which gonadotropin-releasing hormone (GnRH) neurons are genetically tagged with green fluorescent protein for identification in the intact brain. Fish have multiple populations of GnRH neurons, and their functions are dependent on their location in the brain and the GnRH gene that they express1 . We have focused our demonstration on GnRH3 neurons located in the terminal nerves (TN) associated with the olfactory bulbs using the intact brain of transgenic medaka fish (Figure 1B and C). Studies suggest that medaka TN-GnRH3 neurons are neuromodulatory, acting as a transmitter of information from the external environment to the central nervous system; they do not play a direct role in regulating pituitary-gonadal functions, as do the well-known hypothalamic GnRH1 neurons2, 3 .The tonic pattern of spontaneous action potential firing of TN-GnRH3 neurons is an intrinsic property4-6, the frequency of which is modulated by visual cues from conspecifics2 and the neuropeptide kisspeptin 15. In this video, we use a stable line of transgenic medaka in which TN-GnRH3 neurons express a transgene containing the promoter region of Gnrh3 linked to enhanced green fluorescent protein7 to show you how to identify neurons and monitor their electrical activity in the whole brain preparation6.

In this video, we will demonstrate how to record electrical activity from identified single neurons in a whole brain preparation, which preserves complex neural circuits. We use transgenic fish in which gonadotropin-releasing hormone (GnRH) neurons are genetically tagged with a fluorescent protein for identification in the intact brain preparation.

Understanding the cell physiology of neural circuits that regulate complex behaviors is greatly enhanced by using model systems in which this work can be ...

Whole Mount Immunolabeling of Olfactory Receptor Neurons in the Drosophila Antenna

Odorant molecules bind to their target receptors in a precise and coordinated manner. Each receptor recognizes a specific signal and relays this information to the brain. As such, determining how olfactory information is transferred to the brain, modifying both perception and behavior, merits investigation. Interestingly, there is emerging evidence that cellular transduction and transcriptional factors are involved in the diversification of olfactory receptor neuron. Here we provide a robust whole mount immunological labeling method to assay in vivo olfactory receptor neuron organization. Using this method, we identified all olfactory receptor neurons with anti-ELAV antibody, a known pan-neural marker and Or49a-mCD8::GFP, an olfactory receptor neuron specifically expressed in Nba neuron using anti-GFP antibody.

Whole Mount Immunolabeling of Olfactory Receptor Neurons in the Drosophila Antenna

Herein we describe the process of whole mount immunostaining of Drosophila antennae, which enables us to better understand the molecular mechanisms involved in the diversification of olfactory receptor neurons (ORN)s.

Odorant molecules bind to their target receptors in a precise and coordinated manner. Each receptor recognizes a specific signal and relays this ...

A Guide to In vivo Single-unit Recording from Optogenetically Identified Cortical Inhibitory Interneurons

A major challenge in neurophysiology has been to characterize the response properties and function of the numerous inhibitory cell types in the cerebral cortex. We here share our strategy for obtaining stable, well-isolated single-unit recordings from identified inhibitory interneurons in the anesthetized mouse cortex using a method developed by Lima and colleagues1. Recordings are performed in mice expressing Channelrhodopsin-2 (ChR2) in specific neuronal subpopulations. Members of the population are identified by their response to a brief flash of blue light. This technique &#8211; termed &#8220;PINP&#8221;, or Photostimulation-assisted Identification of Neuronal Populations &#8211; can be implemented with standard extracellular recording equipment. It can serve as an inexpensive and accessible alternative to calcium imaging or visually-guided patching, for the purpose of targeting extracellular recordings to genetically-identified cells. Here we provide a set of guidelines for optimizing the method in everyday practice. We refined our strategy specifically for targeting parvalbumin-positive (PV+) cells, but have found that it works for other interneuron types as well, such as somatostatin-expressing (SOM+) and calretinin-expressing (CR+) interneurons.

A Guide to In vivo Single-unit Recording from Optogenetically Identified Cortical Inhibitory Interneurons

Here we describe our strategy for obtaining stable, well-isolated single-unit recordings from identified inhibitory interneurons in the anesthetized mouse cortex. Neurons expressing ChR2 are identified by their response to blue light. The method uses standard extracellular recording equipment, and serves as an inexpensive alternative to calcium imaging or visually-guided patching.

A major challenge in neurophysiology has been to characterize the response properties and function of the numerous inhibitory cell types in the cerebral ...

Perforated Patch-clamp Recording of Mouse Olfactory Sensory Neurons in Intact Neuroepithelium: Functional Analysis of Neurons Expressing an Identified Odorant Receptor

Analyzing the physiological responses of olfactory sensory neurons (OSN) when stimulated with specific ligands is critical to understand the basis of olfactory-driven behaviors and their modulation. These coding properties depend heavily on the initial interaction between odor molecules and the olfactory receptor (OR) expressed in the OSNs. The identity, specificity and ligand spectrum of the expressed OR are critical. The probability to find the ligand of the OR expressed in an OSN chosen randomly within the epithelium is very low. To address this challenge, this protocol uses genetically tagged mice expressing the fluorescent protein GFP under the control of the promoter of defined ORs. OSNs are located in a tight and organized epithelium lining the nasal cavity, with neighboring cells influencing their maturation and function. Here we describe a method to isolate an intact olfactory epithelium and record through patch-clamp recordings the properties of OSNs expressing defined odorant receptors. The protocol allows one to characterize OSN membrane properties while keeping the influence of the neighboring tissue. Analysis of patch-clamp results yields&#160;a precise quantification of ligand/OR interactions, transduction pathways and pharmacology, OSNs&#39; coding properties and their modulation at the membrane level.&#160;

Analyzing the physiological properties of olfactory sensory neurons still faces technical limitations. Here we record them through perforated patch-clamp in an intact preparation of the olfactory epithelium in gene-targeted mice. This technique allows the characterization of membrane properties and responses to specific ligands of neurons expressing defined olfactory receptors.

Analyzing the physiological responses of olfactory sensory neurons (OSN) when stimulated with specific ligands is critical to understand the basis of ...

Electrophysiological Method for Recording Intracellular Voltage Responses of Drosophila Photoreceptors and Interneurons to Light Stimuli In Vivo

Voltage responses of insect photoreceptors and visual interneurons can be accurately recorded with conventional sharp microelectrodes. The method described here enables the investigator to measure long-lasting (from minutes to hours) high-quality intracellular responses from single Drosophila R1-R6 photoreceptors and Large Monopolar Cells (LMCs) to light stimuli. Because the recording system has low noise, it can be used to study variability among individual cells in the fly eye, and how their outputs reflect the physical properties of the visual environment. We outline all key steps in performing this technique. The basic steps in constructing an appropriate electrophysiology set-up for recording, such as design and selection of the experimental equipment are described. We also explain how to prepare for recording by making appropriate (sharp) recording and (blunt) reference electrodes. Details are given on how to fix an intact fly in a bespoke fly-holder, prepare a small window in its eye and insert a recording electrode through this hole with minimal damage. We explain how to localize the center of a cell's receptive field, dark- or light-adapt the studied cell, and to record its voltage responses to dynamic light stimuli. Finally, we describe the criteria for stable normal recordings, show characteristic high-quality voltage responses of individual cells to different light stimuli, and briefly define how to quantify their signaling performance. Many aspects of the method are technically challenging and require practice and patience to master. But once learned and optimized for the investigator's experimental objectives, it grants outstanding in vivo neurophysiological data.

Electrophysiological Method for Recording Intracellular Voltage Responses of Drosophila Photoreceptors and Interneurons to Light Stimuli In Vivo

Sharp microelectrodes enable accurate electrophysiological characterization of photoreceptor and visual interneuron output in living Drosophila. Here we show how to use this method to record high-quality voltage responses of individual cells to controlled light stimulation. This method is ideal for studying neural information processing in insect compound eyes.