Name: utilizing combined methodologies to define the role of plasma membrane delivery during axon branching and neuronal morphogenesis
Uploaded: 2016-03-16T14:00:00
Description: Watch this Scientific Journal Video about Utilizing Combined Methodologies to Define the Role of Plasma Membrane Delivery During Axon Branching and Neuronal Morphogenesis at JoVE.com

Detta arbete stöddes av National Institutes of Health: RO1-GM108970 (SLG) och F31-NS087837 (CW).

Uttalande av forskningsetik: Alla försök med djur som beskrivs häri omfattas av de regler och föreskrifter i UNC kommittén för djurs Care och NIH standarder för vård och användning av försöksdjur. 1. Beredning och plätering av dissocierade kortikal nervceller <ol><li> Avliva tidsinställda-dräktiga honor av CO 2 inandning följt av halsdislokation. Ta bort hela hjärnor från skallarna av embryonala dag 15,5 (E15.5) möss och microdissect cortex fr?...

<ol>
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Axon branching is a fundamental neurodevelopmental process and underpins the vast neuroconnectivity of the mammalian nervous system. Understanding the mechanisms involved in localized plasma membrane expansion is integral to our understanding of both normal and pathological neurodevelopment. The use of a multipronged approach incorporating both population level and single cell level methodologies enhances reproducibility and increases spatial and temporal resolution without compromising population level analysis. At the ...

Recent estimates suggest that the human brain contains 1011 neurons with 1014 synaptic connections1, highlighting the importance of axon branching in vivo. Extracellular axon guidance cues such as netrin-1 guide axons to appropriate synaptic partners and stimulate axonal branching, thereby increasing synaptic capacity2-5. Netrin-1-dependent axonal arborization involves substantial plasma membrane expansion6, which we hypothesized requires delivery of additional membrane components via SNARE complex dependent exocytic vesicle fusion7. 
Investigating the role of SNARE-mediated exocytosis in netrin-1 dependent axon branching is complicated by several factors. First, the heterogeneity of cortical neurons increases the sample size required to identify significant effects, complicating single cell techniques like imaging. Second, although biochemical techniques permit observation of changes that occur at the population level, they lack the temporal and spatial resolution necessary to localize plasma membrane expansion to the axon in the time frame of axon branching. Lastly, although axon branches form over hours, the cellular changes that contribute to axonal extension may begin within minutes and occur on the order of seconds, thus extending the temporal scope for experimental consideration. 
We outline a multi-technique approach that addresses these diverse temporal and spatial scales of exocytosis and axon branching, and thus enhances our understanding of the fundamental cellular mechanisms. Utilizing these approaches provides evidence that supports a critical role for SNARE-mediated exocytosis in axon branching.

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			<td height="40" style="height:40px;width:179px;">6-well tissue culture treated plates</td>
			<td style="width:99px;">Olympus Plastics</td>
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			<td style="width:76px;"></td>
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			<td height="61" style="height:61px;width:179px;">Neurobasal media</td>
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			<td height="62" style="height:62px;width:179px;">Supplement B27</td>
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			<td height="21" style="height:21px;width:179px;">HEPES</td>
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			<td height="42" style="height:42px;width:179px;">Poly-D-Lysine</td>
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			<td height="81" style="height:81px;width:179px;">Botulinum A toxin BoNTA</td>
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			<td height="41" style="height:41px;width:179px;">Rabbit polyclonal anti human VAMP2</td>
			<td style="width:99px;">Cell signaling</td>
			<td style="width:76px;">11829</td>
			<td style="width:187px;"></td>
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			<td height="61" style="height:61px;width:179px;">Mouse monoclonal anti rat Syntaxin1A</td>
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			<td>sc-12736</td>
			<td style="width:187px;"></td>
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		<tr height="61">
			<td height="61" style="height:61px;width:179px;">Goat polyclonal anti human SNAP-25</td>
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			<td>sc-7538</td>
			<td style="width:187px;"></td>
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			<td height="41" style="height:41px;width:179px;">Mouse monoclonal anti human &#946;III-tubulin&#160;</td>
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			<td height="81" style="height:81px;width:179px;">Alexa Fluor 568 and Alexa Fluor 488 phalloidin, or Alexa Fluor 647</td>
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			<td style="width:76px;"></td>
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			<td height="121" style="height:121px;width:179px;">LI-COR IR-dye secondary antibodies</td>
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			<td style="width:187px;">800 donkey anti-mouse, 680 donkey anti rabbit, 680 donkey anti goat</td>
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		<tr height="61">
			<td height="61" style="height:61px;width:179px;">0.2um pore size nitrocellulose membrane</td>
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			<td style="width:187px;"></td>
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		<tr height="41">
			<td height="41" style="height:41px;width:179px;">Paraformaldehyde</td>
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			<td style="width:76px;">O-4042-500</td>
			<td style="width:187px;"></td>
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			<td height="41" style="height:41px;width:179px;">Triton-X100</td>
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		</tr>
		<tr height="41">
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			<td height="42" style="height:42px;width:179px;">Name</td>
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			<td style="width:76px;">Catalog Number</td>
			<td style="width:187px;">Comments</td>
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			<td height="42" style="height:42px;width:179px;">Alternative Validated Antibodies</td>
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			<td height="61" style="height:61px;width:179px;">&#160;Mouse Monoclonal Synaptobrevin 2 (VAMP2)</td>
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utilizing combined methodologies to define the role of plasma membrane delivery during axon branching and neuronal morphogenesis

During neural development, growing axons extend to multiple synaptic partners by elaborating axonal branches. Axon branching is promoted by extracellular guidance cues like netrin-1 and results in dramatic increases to the surface area of the axonal plasma membrane. Netrin-1-dependent axon branching likely involves temporal and spatial control of plasma membrane expansion, the components of which are supplied through exocytic vesicle fusion. These fusion events are preceded by formation of SNARE complexes, comprising a v-SNARE, such as VAMP2 (vesicle-associated membrane protein 2), and plasma membrane t-SNAREs, syntaxin-1 and SNAP25 (synaptosomal-associated protein 25). Detailed herein isa multi-pronged approach used to examine the role of SNARE mediated exocytosis in axon branching. The strength of the combined approach is data acquisition at a range of spatial and temporal resolutions, spanning from the dynamics of single vesicle fusion events in individual neurons to SNARE complex formation and axon branching in populations of cultured neurons. This protocol takes advantage of established biochemical approaches to assay levels of endogenous SNARE complexes and Total Internal Reflection Fluorescence (TIRF) microscopy of cortical neurons expressing VAMP2 tagged with a pH-sensitive GFP (VAMP2-pHlourin) to identify netrin-1 dependent changes in exocytic activity in individual neurons. To elucidate the timing of netrin-1-dependent branching, time-lapse differential interference contrast (DIC) microscopy of single neurons over the order of hours is utilized. Fixed cell immunofluorescence paired with botulinum neurotoxins that cleave SNARE machinery and block exocytosis demonstrates that netrin-1 dependent axon branching requires SNARE-mediated exocytic activity.

Utnyttja in vitro biokemiska tekniker för att analysera mängden av SDS-resistenta SNARE-komplex i en population av nervceller. Figur 1 visar det resulterande western blöt efter fullföljande av den SDS-resistenta SNARE-komplex analys sonde för SNAP-25, syntaxin1A och VAMP2. TIRF mikroskopi vid basalcellmembranet ger högupplösta bilder av enskilda exocytiska fusions händelser i enskilda celler. ...

Watch this Scientific Journal Video about Utilizing Combined Methodologies to Define the Role of Plasma Membrane Delivery During Axon Branching and Neuronal Morphogenesis at JoVE.com

Utilizing Combined Methodologies to Define the Role of Plasma Membrane Delivery During Axon Branching and Neuronal Morphogenesis

Light microscopy techniques coupled with biochemical assays elucidate the involvement of SNARE-mediated exocytosis in netrin-dependent axon branching. This combination of techniques permits identification of molecular mechanisms controlling axon branching and cell shape change.

Med hjälp av kombinerade Metoder för att definiera rollen av plasmamembranet leverans under Axon förgrening och Neuronal Morphogenesis

During neural development, growing axons extend to multiple synaptic partners by elaborating axonal branches. Axon branching is promoted by extracellular ...

The overall goal of this procedure is to make quantifiable observations of the temporal and spatial occurrence of neuronal exocytic vesicle fushion and axon branching. This method can help answer key questions in the neuroscience field, such as when and where vesicle fusion inserts membrane material into the expanding plasma membrane during neuronal development. The main advantage of this technique is that it combines live cell imaging to acquire both high spatial and temporal resolution in single cells and biochemical approaches to acquire population based information.After culturing and simulating cortical neurons with Netrin-1 or a control according to the protocol text. Aspirate PBS from the first well of a condition and replace with 250 microliters of homogenization buffer. Incubate on ice for five minutes, and then using a cell lifter, homogenize the cells on ice.Aspirate the PBS from the next well of the same condition and add the recently homogenized mixture to the well which will increase protein concentrations. Next, transfer the homogenized solution to a pre-cooled 1.6 milliliter microfuge tube on ice, and add 20%Triton X-100 to reach a final concentration of 1%Then with a 1, 000 microliter pipette, triturate the mixture ten times while minimizing bubbles. Incubate the tubes on ice for two minutes to solubilize the proteins.Then centrifuge at 6, 010 RCF at 4 degrees Celsius for 10 minutes to pellet the non-solubilized material. Transfer the lie state supernatant into a new chilled 1.6 milliliter tube on ice. Next, use the Bradford assay to determine protein concentration.Then, use homogenization buffer with 1%Triton X-100 and 5X sample buffer supplemented with BME to dilute the samples to a final concentration of 3-5 milligrams per milliliter. Divide each experimental sample evenly into two tubes. Then incubate one sample at 37 degrees Celsius for 30 minutes, and the other at 100 degrees Celsius for 30 minutes.Invert the tubes intermittently to keep samples in solution. Then carry out SDS page and Western blotting according to the text protocol. After setting up the TIRF microscope and the sample and finding a neuronal focal plane according to the text protocol.Start the laser software and connect to the laser control software. Set the illumination to wide field and select the objective. Then set the refractive index of the sample and adjust the laser intensity by unchecking TTL for the 491 laser.Imaging parameter optimization is important during imaging of floor intact exocytic vesicles to avoid focus drift and phototoxicity while producing images of high signal to noise ratio sufficient for analysis. Adjust the slider to 100 and then bring it back down to a value between 20 and 40. Then recheck TTL.Next, focus on the sample again in transmitted light illumination. Then in the imaging software, select the 491 laser illumination and open the shutter. Place the condenser upside down on the optical bench so as not to scratch the lens.Fine adjust the focal point of the laser on the ceiling and with the condenser removed, center the point to the center of the closed field diaphragm. Then replace the condenser and in the TIRF software sent the penetration depth to 110 nanometers. Then switch from wide field illumination to TIRF illumination mode for imaging.Now, using wide field epifluorescence find VAMP2 fluorent expressing cells through the oculars. Then to reduce photobleaching and phototoxicity, adjust the imaging parameters to maximize the signal to noise ratio and dynamic range using minimal exposure time and laser intensity. Set continuous auto focus per cell.Then acquire a time lapse image set with acquisition occurring every 0.5 seconds for five minutes. For the Netrin-1 stimulated condition in a laminar flow hood, add to a final concentration of 500 nanograms per milliliter of Netrin-1 to a dish of cells and return the dish to the incubator for one hour prior to imaging. To quantify the frequency of exocytic events normalized per cell area and time.In ImageJ, open image stacks by dragging the file into the window or by choosing File, Open, file name. To remove stable fluorescent signals that do not represent vesicle fusion events, use Image, Stack, Z Project, Projection type Average Intensity. To create an average Z Projection of the entire stack.Subtract the resulting mean image from each image in the timelapse using Process, Image Calculator, Image 1 your stack, Operation Subtract image two. Resulting in a newly created Z Projection. This will emphasize exocytic events.Now by eye, count exocytic fushion events, which can be identified as spots of diffraction limited fluorescent signals that rapidly diffuse as VAMP2 fluoren diffuses within the plasma membrane. Highlight the first image with Image, Adjust, Threshold, and adjust the slider until the entire cell is threshold highlighted. Then under Analyze, choose Set Measurements and check the area and display label.With the wand tracing tool, set the thresholded cellular area and press M to measure. Transfer the collected data to a spreadsheet according to the text protocol. At two days in-vitro, place the glass bottom imaging dish containing untransfected neurons in a pre-warmed humid environmental chamber.Utilize a microscope equipped with a six DX plan apochromat 1.4 NA DIC objective lens and a high numerical aperture condenser for the best image quality and resolution. Next, with transmitted light illumination adjust the focal plane to find neurons through oculars. For DIC imaging of axon branching, proper setup of cooler illumination will be integral for image optimization and is critical to producing analyzable results.Then, with the neurons of interest within the field of view, use the multi-area acquisition function in the imaging software to find and save the XYZ locations of at least six cells. Now, add to a final concentration of 250 nanograms per milliliter of Netrin-1 or other factor of interest to simulate the cells and press start multi-area acquisition. Sequentially acquire images at each position every 20 seconds for 24 hours.Pausing acquisition and refocusing as necessary. Within the imaging software, review images by choosing Apps, Review Multi Dimensional Data and open the desired file. Identify stable axon branches that formed during the imaging session.Use the trace region tool to measure a stable axon branch from the base of the axon to the tip. After treating neurons with Netrin and botulinum toxin and fixing and immunostaining, and immunostaining for beta-3 tubolin and actin according to the text protocol. Use an inverted microscope to collect wide field epifluorescence images.Open an image stack in ImageJ and to manually analyze the branching use line, segmented line and trace the axon which is defined as the longest neurite extending from the soma. With Analyze, Tools, ROI Manager, save the axon tracing as a region of interest. Then trace and save each axon branch, which is defined as a neurite greater than or equal to 20 micrometers in length.Include only primary branches in the analysis. Shown here is a Western blot following the completion of the SDS resistant SNARE complex assay. Probed for SNAP25, Syntaxin 1A, and VAMP2.SNARE proteins in complex, an identifiable monomers are shown here. An example of a VAMP2 fluroen mediated exocytic event occurring over time in a cortical neuron is shown here. The zoomed insets denote the soma, an axon branch, and an axonal growth cone showing the spatial utility of this assay.Circles detonate single exocytic fusion events, which can be seen via TIRF microscopy. This time lapse DIC imaging shows the Netrin stimulated formation of an axon branch in real time. These locations denote the initial protrusion from a branch site.These represent fully formed stable branches of at least 20 micrometers measured from the main axon to the branch tip. In this experiment, cortical neurons at 3 DIV were either treated with Netrin-1, which stimulates branching or botulinum A toxin, which cleaves SNAP25, a component of the SNARE complex and blocks exocytosis. The results demonstrate that SNARE mediated exocytosis is requisite for Netrin dependent branching.Once mastered, the DIC imaging can be completed in a single overnight imaging session. TIRF imaging of individual exocytic events can be managed in 4-5 hours. The SNARE complex formation biochemistry protocol can be performed in two hours.While attempting these procedures, it's important to remember to pace yourself and not rush any single step. Each procedure requires attention and patience for the best results. Following this procedure, other methods like cotransfection of tagged vesicle components with tagged candidate cargos can be performed to answer additional questions.Like what is the cargo of the exocytic vesicles? After it's development, this technique paved the way for researchers in the field of neuroscience to explore neuritogenesis, axon branching, and other stages in morphogensis in any dissociated neuronal culture. After watching this video, you should have a good understanding of how to observe and quantify the spatial and temporal nature of neuronal exocytic vesicle fusion events corresponding to changes in neuronal morphogensis.Don't forget that working with botulinum toxin or high powered lasers can be extremely hazardous and precautions such as wearing proper safety garments and using the microscope safety lock mechanism should always be taken while performing this procedure.

Research

JoVE Journal

Neuroscience

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