Name: isolation and culture of dissociated sensory neurons from chick embryos
Uploaded: 2014-09-24T14:00:00.000+00:00
Duration: 11 min 16 s
Description: Watch this Scientific Journal Video about Isolation and Culture of Dissociated Sensory Neurons From Chick Embryos at JoVE.com

We would like to thank Alison Philbrook, Belinda Barbagallo and Michael Francis for insightful comments on this paper. Research reported in this publication was supported by an R15 AREA award 1R15NS070172-01A1 awarded to MLL.

1. Coverslip Preparation: Acid Wash and Bake
<ol>
	<li>At least 2&#160;days prior to dissection (step 2), begin the following steps to prepare coverslips. Perform the acid wash step to remove oils and thoroughly clean coverslips.</li>
	<li>Load coverslips in porcelain holder that vertically positions coverslips and prevents them from touching each other. Submerge holder and coverslips into glass histology container filled with 2 M hydrochloric acid (HCl). Alternatively, if porcelain holder is not available, spread ~20 coverslips horizontally to cover the bottom of 100 mm glass Petri dish and submerge coverslips in 2 M HCl.</li>
	<li>Place glass vessel (with coverslips submerged in acid) on rocker table in fume hood and allow gentle rocking for at least 5 hr at room temperature. Alternatively, acid wash coverslips overnight under the same conditions.</li>
	<li>Wash coverslips with distilled H2O(dH2O) by transferring porcelain holder loaded with coverslips from 2 M HCl to a clean glass histology container filled with dH2O. Alternatively, decant 2 M HCl from glass Petri dish with coverslips and refill with dH2O.</li>
	<li>Wash by decanting dH2O again and refilling glass vessel with fresh dH2O. Repeat for a total of 3&#160;quick washes.</li>
	<li>Begin longer washing regimen by returning glass vessel (with coverslips and dH2O) onto rocker. Allow for gentle agitation for 10-30 min at room temperature. Then, decant dH2O and add fresh dH2O. Repeat for a total of at least ten washes. Alternatively, continue washing overnight.</li>
	<li>Place washed coverslips into furnace preheated to 350 &#176;C. If using porcelain holder, remove holder from dH2O-filled glass container and then place holder with coverslips directly into the furnace. If using a glass Petri dish, decant dH2O and place the glass dish with coverslips into the furnace.</li>
	<li>Bake coverslips for at least five hours or overnight at 350 &#176;C.</li>
	<li>After baking is complete, remove coverslips from porcelain holder with fine forceps and place into sterile 100 mm glass Petri dish. Leave coverslips that were not originally placed in porcelain holder in the glass Petri dish.</li>
</ol>
2. Chick Dissection and Isolation of DRGs
<ol>
	<li>Remove fertile, staged White Leghorn chick egg from incubator (held at 37-38.5 &#176;C with gentle rocking). 
	NOTE: Previous studies have used embryonic day 7-10 for isolation of DRGs2,8,11-13,16.</li>
	<li>Place selected egg in laminar flow hood. Conduct all procedures listed below under aseptic conditions in the laminar flow hood with sterile solutions and instruments. Pre-warm all solutions in a 37 &#176;C water bath.</li>
	<li>Crack egg and place contents into a plastic 100 mm Petri dish. Use standard forceps to transfer embryo to another 100 mm Petri dish.</li>
	<li>Using a Pasteur pipette, add warmed 1x&#160;PBS to Petri dish to keep tissue wet. Decapitate embryo by pinching neck with fine forceps. Transfer body to another clean 100 mm Petri dish.</li>
	<li>Add warm F12HS10 (Ham&#8217;s F12, 10 mM HEPES, 100 units/ml penicillin, 0.1 mg/ml streptomycin, 10% fetal bovine serum) to dish with Pasteur pipette to keep tissue wet. Use forceps to position embryo on its dorsal side (Figure 1A).</li>
	<li>Place 100 mm plastic Petri dish containing embryonic tissue onto a binocular stereovision dissecting microscope in laminar flow hood.&#160;Use fine forceps to make a vertical midline incision from&#160;tail to neck by pinching the developing dermis to expose the heart, lung and other organs. Alternatively, make a series of small tears to expose internal organs.</li>
	<li>Gently use 2&#160;sets of sterile fine forceps to: a) grasp the neck and b) grasp the aorta or other tissue immediately superior to the heart and pull towards the tail, eviscerating the animal.</li>
	<li>Apply warm F12HS10 with Pasteur pipette to tissue. Use forceps to remove any remaining cardiovascular, respiratory or digestive organs to expose the developing ribs, vertebral column and DRGs (Figures 1B-1D).</li>
	<li>Under the dissecting microscope, use fine forceps to further remove organs and collect DRGs along both sides of lumbar vertebral column, inferior to the ribs. Collect DRGs by plucking intact DRGs from the embryo. Pinch and sever the roots that reach from the DRG towards the spinal cord and grasping the developing nerve that reaches from the DRG towards the periphery or vice versa.</li>
	<li>Place intact DRGs into a 35 mm culture dish filled with warm F12HS10. Remove any excess tissue, such as the dorsal or ventral roots that may have adhered to DRGs, from the intact DRGs in 35 mm dish by pinching with fine forceps.</li>
	<li>To obtain DRGs superior to the lumbar region, remove the ventral half of the thoracic and cervical vertebral column. This is done by making a cut in the developing vertebral column perpendicular to the spinal cord axis in the upper cervical region and another cut in the upper lumbar region. Then, make cuts parallel to the spinal cord axis along the right and left sides of the vertebral column. Lift the ventral half of the vertebral column from the embryo, which exposes the exposes the spinal cord (Figures 1E-1F).</li>
	<li>To allow easy access to DRGs, remove the thoracic and cervical spinal cord by grasping the spinal cord with fine forceps. Use the forceps to lift the spinal cord out of the vertebral column. As an approximation, the thoracic spinal cord is at the level of ribs and the cervical area is superior to the ribs.</li>
	<li>Collect intact thoracic and cervical DRGs with fine forceps and place them in warm F12HS10 with other DRGs. Remove excess tissue that may adhere to DRGs.</li>
	<li>Rinse interior of a new glass Pasteur pipette with F12HS10 to help prevent DRGs from sticking to walls of pipette. Use rinsed pipette to transfer all DRGs and F12HS10 from small Petri dish to a sterile 15 ml conical tube and immediately proceed to step 3. 
	NOTE: Additional embryos can be dissected to increase number of&#160;DRGs. DRGs should be kept in F12HS10 at 37 &#176;C until ready for step 3.</li>
</ol>
3. Dissociation, Enriching, and Culturing DRG Neurons &#8211; Part 1
<ol>
	<li>Place conical tube with intact DRGs into centrifuge and gently spin (200 x g) for 2-3 min. Confirm that DRGs have sunk to bottom of tube. If not, spin again.</li>
	<li>Using a pipette, gently remove F12HS10, leaving DRG pellet undisturbed. Add 2 ml of 1x&#160;calcium and magnesium free (CMF) PBS, dislodging the pellet of DRGs. Spin again and remove CMF PBS while leaving the DRG pellet intact. Repeat this wash step for a total of three washes to remove fetal bovine serum in F12HS10, which would interfere with trypsin digestion in next step.</li>
	<li>Add 2 ml of warmed trypsin to 15 ml tube containing 2 ml CMF PBS and DRGs. Place tube in 37 &#176;C water bath for 10-15 min&#160;to digest DRGs into dissociated cells.</li>
	<li>During incubation, make F12H + supplement containing media (Ham&#8217;s F12, 10 mM HEPES 100 units/ml penicillin, 0.1 mg/ml streptomycin, 10 ng/ml NT3, 10 ng/ml NGF, 200 mM l-glutamine and N2) and warm in 37 &#176;C water bath. Typically, 10 ml of total media is sufficient for 4-5 35 mm dishes of primary sensory neurons. Also begin thawing laminin-1 for coating coverslips (step 4).</li>
	<li>Gently triturate DRGs in trypsin solution with p1000 pipette and visually inspect for absence of intact DRGs. Continue trituration until intact DRGs are no longer seen by eye and/or allow for longer trypsin incubation in 37 &#176;C water bath until intact DRGs are dissociated. To protect DRG neurons from damage, avoid air bubbles during trituration and limit trypsin digestion to &#60;30 min.</li>
	<li>Centrifuge tube containing dissociated DRGs and trypsin at 200 x g for 3-5 min&#160;to form pellet. Spin longer if needed until pellet is formed.</li>
	<li>Carefully aspirate trypsin without disrupting pellet. Add 2 ml of F12HS10 to pellet. Gently triturate DRGs with a p1000 pipette tip.</li>
	<li>Transfer all contents from 15 ml conical tube into 100 mm culture dish. Rinse the tube with 8 ml F12HS10 and transfer it to the culture dish, 2 ml at a time for a total of 10 ml. This rinsing step helps collect cells that may have remained adhered to the walls of the tube.</li>
	<li>Place 100 mm culture dish (with 10 ml F12HS10 and dissociated DRG cells) into a humidified 37 &#176;C incubator for 3 hr. 
	NOTE: CO2 is not required in the incubator because HEPES buffers media pH in the absence of CO2. During incubation, glial cells bind to surface of tissue culture plastic and neurons tend to loosely adhere to glial bed.</li>
</ol>
4. Coating Acid Washed and Baked Coverslips with Laminin-1
<ol>
	<li>Thaw sterile aliquots of frozen laminin-1 on ice.</li>
	<li>Under sterile conditions, add 1 ml of sterile 1x&#160;PBS to 50 &#956;l aliquot of laminin-1.</li>
	<li>Use a spectrophotometer to obtain an absorbance value of laminin-1 at 280 nm. Use this value in the following equation to determine the concentration of laminin-1.</li>
</ol>
ABS 280 = (concentration mg/ml) * (extinction coefficient of protein) 
The extinction coefficient for laminin-1 is 0.86.
<ol start="4">
	<li>Under sterile conditions, dilute laminin-1 with 1X PBS to obtain the concentrations 1 mg/ml and 20 mg/ml. Use these two applied concentrations of laminin-1 to achieve a ten-fold difference of laminin-1 bound to the coverslip (30 ng/cm2 and 300 ng/cm2, respectively) after incubation7,8,10.</li>
	<li>In a laminar flow hood, use fine forceps to place one acid-washed and baked coverslip into the bottom of one 35 mm culture dish. Repeat as necessary to obtain the number of dishes needed.</li>
	<li>Subject the coverslips to UV light for 20-30 min&#160;to further ensure sterilization. Keep dish lid off during this step.</li>
	<li>Add 400 &#956;l of prepared laminin-1 to each glass coverslip. Use pipette tip to spread laminin-1 to ensure full coverage of coverslip. Surface tension will allow laminin-1 to remain on coverslip and not spread onto bottom of culture dish, which is required.</li>
	<li>Place lid onto dish and allow laminin-1 to incubate for 2-3 hr&#160;at room temperature (3 hr&#160;is optimal).</li>
	<li>After laminin-1 incubation, rinse coverslips using aseptic technique with sterile PBS in laminar flow hood. Remove solution on coverslip and add 400 &#956;l of PBS. Wait 5-10 min. Repeat for a total of 3&#160;rinses.</li>
	<li>Leave PBS on coverslip after last rinse. Do not break surface tension during rinsing and do not allow coverslips to dry out. Leave lid on until ready to plate dissociated neurons onto the coverlip.</li>
</ol>
5. Dissociation, Enriching, and Culturing DRG Neurons &#8211; Part 2
<ol>
	<li>After incubation, use a 10 ml sterile pipette to gently rinse the bottom of the 100 mm dish containing dissociated DRG cells. Hold dish at ~45&#176;&#160;angle, pull ~7 ml of F12HS10 with pipette aid, then gently expel 7 ml onto approximately 1/3 of dish. Repeat 5x, gently dislodging neurons.</li>
	<li>Rotate dish and repeat rinsing procedure, for another six rinses, on another 1/3 of the dish. Repeat procedure again for remaining 1/3 of dish. In this way, gently rinse the entire bottom of the dish with F12HS10 to remove neurons.</li>
	<li>Using same pipette, transfer F12HS10 containing neurons from 100 mm dish to 15 conical tube. Centrifuge for 5-10 min&#160;at 200 g to pellet cells.</li>
	<li>Remove F12HS10, leaving pellet undisturbed. Resuspend pellet with 2 ml of warmed F12H + supplements.</li>
	<li>Use a hemocytometer to determine cell density.</li>
	<li>Dilute cells as necessary with F12H + supplements to obtain desired plating concentration (120,000 cells/ml for coverslips coated with 1 &#956;g/ml laminin-1 and 40,000 cells/ml for coverslips coated with 20 &#956;g/ml laminin-18,16).</li>
	<li>Remove PBS from laminin-coated coverslips and immediately place 400 &#956;l of cells onto coverslips. Carefully transfer dish to a humidified, 37 &#176;C cell culture incubator. Allow to incubate for at least 1 hr and up to 3 hr&#160;to allow neurons to adhere to laminin-1.</li>
	<li>Under sterile conditions, gently flood 35 mm dishes containing neurons with 1.6 ml of F12H + supplements. 
	NOTE: At this time, surface tension on coverslip can be broken. Neurons have adequately adhered to laminin-1 on coverslip.</li>
	<li>Return cells to incubator and incubate overnight. Perform experiments such as immunocytochemistry the following day.</li>
</ol>
6. Immunocytochemistry
<ol>
	<li>Prior to immunocytochemistry, warm fixative solution (4% paraformaldehyde, 30% sucrose 2X PBS) in 37 &#176;C water bath. 
	NOTE: Before fixing cells, treat with various reagents, such as netrin-1, Mn2+, sonic hedgehog, semaphorin, and ephrin16,29-31.</li>
	<li>Slowly remove 1 ml of the 2 ml of F12H + supplements from culture dish. Gently add 1 ml of warmed fixative solution. Allow to incubate at room temperature for 10-15 min.</li>
	<li>Carefully remove fixative solution and add 2 ml PBS. Apply solution towards edge of dish, avoiding possible dislodging of fixed cells due to application of PBS. Incubate at room temperature for 5 min.</li>
	<li>Repeat PBS wash for a total of 5 washes. Do not allow cells to dry during any step of immunocytochemistry.</li>
	<li>Remove PBS. Apply 1 ml of blocking solution (0.1% Triton-X, 1X PBS, 5% normal goat serum). Incubate for 1 hr at room temperature. Alternatively, to stain surface molecules, do not use Triton-X in blocking solution8.</li>
	<li>Dilute primary antibodies into blocking solution per manufacture&#8217;s recommendation. Use 1:500 for antibodies against NCAM and activated &#946;1 integrins16. Remove blocking solution, add 1 ml of primary antibody solution and incubate for 1 hr at room temperature or overnight at 4 &#176;C.</li>
	<li>Remove primary antibody solution and add 2 ml of 1X PBS. Incubate for 5-10 min&#160;at room temperature. Repeat for a total of 4 PBS washes. Washes can be extended, if needed.</li>
	<li>Dilute secondary antibody 1:1,000 in blocking solution. Remove PBS, add 1 ml secondary antibody solution and incubate for 1 hr at room temperature. 
	NOTE: Secondary antibodies are light sensitive. Keep solutions and cells in the dark as much as possible from this point forward.</li>
	<li>Remove secondary antibody solution and rinse 5x&#160;with 1x&#160;PBS, as done previously.</li>
	<li>Apply ~60-80 &#956;l of Fluoromount G onto a microscope slide. Using fine forceps, gently lift coverslip out of dish and lower coverslip into Fluoromount G onto microscope slide. Avoid air bubbles.</li>
	<li>Store slides horizontally at 4 &#176;C in the dark. After 12-24 hr, Fluormount G will polymerize and coverslip will be firmly attached to microscope slide. Image cells after this polymerization step is complete.</li>
</ol>

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G., Kueter, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+expression+of+cell+adhesion+molecules+on+the+growth+cones+of+chick+cutaneous+and+muscle+sensory+neurons.">The expression of cell adhesion molecules on the growth cones of chick cutaneous and muscle sensory neurons.</a> Developmental biology. 167, 563-583 (1995).</li><li>Tosney, K. W., Landmesser, L. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Development+of+the+major+pathways+for+neurite+outgrowth+in+the+chick+hindlimb.">Development of the major pathways for neurite outgrowth in the chick hindlimb.</a> Developmental biology. 109, 193-214 (1985).</li><li>Dontchev, V. D., Letourneau, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nerve+growth+factor+and+semaphorin+3A+signaling+pathways+interact+in+regulating+sensory+neuronal+growth+cone+motility.">Nerve growth factor and semaphorin 3A signaling pathways interact in regulating sensory neuronal growth cone motility.</a> The Journal of neuroscience : the official journal of the Society for Neuroscience. 22, 6659-6669 (2002).</li><li>Munoz, L. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ephrin-A5+inhibits+growth+of+embryonic+sensory+neurons.">Ephrin-A5 inhibits growth of embryonic sensory neurons.</a> Developmental biology. 283, 397-408 (2005).</li><li>Roche, F. K., Marsick, B. M., Letourneau, P. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Protein+synthesis+in+distal+axons+is+not+required+for+growth+cone+responses+to+guidance+cues.">Protein synthesis in distal axons is not required for growth cone responses to guidance cues.</a> The Journal of neuroscience : the official journal of the Society for Neuroscience. 29, 638-652 (2009).</li><li>Condic, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Adult+neuronal+regeneration+induced+by+transgenic+integrin+expression.">Adult neuronal regeneration induced by transgenic integrin expression.</a> Journal of Neuroscience. 21, 4782-4788 (2001).</li><li>Hory-Lee, F., Russell, M., Lindsay, R. M., Frank, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neurotrophin+3+supports+the+survival+of+developing+muscle+sensory+neurons+in+culture.">Neurotrophin 3 supports the survival of developing muscle sensory neurons in culture.</a> Proceedings of the National Academy of Sciences of the United States of America. 90, 2613-2617 (1993).</li><li>Toyofuku, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=FARP2+triggers+signals+for+Sema3A-mediated+axonal+repulsion.">FARP2 triggers signals for Sema3A-mediated axonal repulsion.</a> Nature neuroscience. 8, 1712-1719 (2005).</li><li>Steinmetz, M. P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chronic+enhancement+of+the+intrinsic+growth+capacity+of+sensory+neurons+combined+with+the+degradation+of+inhibitory+proteoglycans+allows+functional+regeneration+of+sensory+axons+through+the+dorsal+root+entry+zone+in+the+mammalian+spinal+cord.">Chronic enhancement of the intrinsic growth capacity of sensory neurons combined with the degradation of inhibitory proteoglycans allows functional regeneration of sensory axons through the dorsal root entry zone in the mammalian spinal cord.</a> The Journal of neuroscience : the official journal of the Society for Neuroscience. 25, 8066-8076 (2005).</li></ol>

The authors have nothing to disclose.

Here we present detailed protocols for isolating and culturing dissociated sensory neurons from a chick embryo. This procedure generates an enriched population of robustly growing neurons in vitro7,8,10,16. Numerous cellular and molecular techniques can be applied to these cultured neurons, including immunocytochemistry, which is described here. This protocol was recently used to quantitatively assess the intensity of immunolabeled activated integrins in sensory growth cones8,16. In these p...

Neurons are complex cells that carry information essential for a variety of functions including sensation, vision, motor movement, learning, and memory. Unique from other cell types, neurons extend arm-like processes, called axons, to form essential neural highways for communication. During development specialized compartments located at the tips of growing axons, called growth cones, navigate through a concert of extracellular cues to lead the axon to its appropriate destination. The intricate molecular mechanisms that underlie growth cone navigation are not fully understood. To better understand these mechanisms, investigators have used cell culture models to study neurons in a defined and simplified in vitro environment. Studying neurons in culture1 has led to significant advances in our understanding of neuronal cell biology including: neuronal differentiation2, cytoskeletal dynamics, endocytosis and trafficking,&#160;dendrite regulation3,4,&#160;axonal regeneration5, and clinical conditions such as neuropathies6. In addition, cultured neurons are highly amenable to a wide range of research techniques including immunocytochemistry, cell surface co-immunoprecipitation, Western blot, transfection, RNAi, and live imaging such as timelapse analysis of growth cone motility. Thus, culturing primary neurons is a powerful approach to elucidate numerous aspects of the cell biology of neurons.
The cell culture model provides investigators with detailed control over environmental conditions and variables. For example, the substrata on which neurons are plated (and grow upon) can be easily manipulated. Here, we provide detailed instructions for generating two distinct substrata, one with a low laminin-1 concentration and the other with saturating concentrations of laminin-1. Surprisingly, different concentrations of the same molecule can have dramatic effects on the internal state of neurons as well as their cell surface composition. For example, intracellular levels of cAMP and surface levels of integrins are significantly different in neurons plated on these two substrata7,8. Additional studies have shown that other molecules, including fibronectin and chondroitin sulfate proteoglycans, impact the expression of cell surface molecules and neuronal motility7-11. In addition, soluble molecules such as neurotrophins and neurotropins also impact cell membrane composition and neuronal motility12-16 and can be easily and accurately manipulated in a cell culture model.
Here, we describe methods to isolate and culture dissociated sensory neurons from chick embryos. This procedure has been used to make significant breakthroughs in neurobiology, including axon outgrowth5,7,8,10,11,16-21 and was modified from a procedure designed to isolate ganglion cells22. There are several advantages to this approach. First, many features of chick dorsal root ganglion (DRG) development are well characterized including the time frame for birth, axon extension, and protein expression profiles2,23-28, thus providing an instructive basis upon which to build informative in vitro experiments. Second, dissociated neuronal cultures allow the investigator to more directly study neurons compared to alternative approaches using intact DRG explants (which contain neurons and non-neuronal cells) and/or mixed cultures containing both dissociated neurons and non-neuronal cells. Third, the procedure described here is straightforward, inexpensive and amenable to undergraduates. Therefore, this technique can be used for research as well as for teaching purposes. Furthermore, minor variations of this protocol should allow fast, high yield purification of neurons from sources other than DRGs. For example, this procedure could be modified to provide neuronally enriched cultures from other tissues such as embryonic forebrain or spinal cord.
Immunocytochemistry protocols have been optimized for these dissociated neuronal cultures and are described in detail here. The procedure for double immunocytochemistry against neural cell adhesion molecule (NCAM) and &#946;1 integrins is provided. Data generated from these immunocytochemical methods have been used to examine the spatial patterning and intensity of several molecules in cultured neurons8,16.

<table><tbody><tr><td>Sterile small culture dishes (35 mm)</td><td>Corning</td><td>430165</td><td></td></tr><tr><td>Sterile large culture dishes (100 mm)</td><td>Falcon</td><td>353003</td><td></td></tr><tr><td>Sterile large Petri dishes (100 mm)</td><td>VWR</td><td>89000-302</td><td></td></tr><tr><td>Glass Petri dish (100 mm)</td><td>VWR</td><td>D108962</td><td></td></tr><tr><td>Fine forceps</td><td>Fine Science Tools</td><td>11251-10</td><td></td></tr><tr><td>Standard forceps</td><td>Fine Science Tools</td><td>1100-12</td><td></td></tr><tr><td>Coverslips (22 x 22 mm)</td><td>Fisher</td><td>12 518 105K</td><td>0.13-0.17 mm thickness is optimal for microscopy</td></tr><tr><td>Porcelin coverslip holder</td><td>Thomas scientific</td><td>8542E40</td><td></td></tr><tr><td>Fetal Bovine serum</td><td>Gibco</td><td>17502-048</td><td>use 50 ml aliquots per 500 ml of Ham&#039;s F12 media</td></tr><tr><td>HCl</td><td>VWR</td><td>VW3204-1</td><td>use at 2 M, can be used twice before discarding</td></tr><tr><td>NaCl</td><td>Sigma</td><td>S9888</td><td>use 5 M NaCl solution for laminin-1 stock solution</td></tr><tr><td>Laminin-1</td><td>Invitrogen</td><td>23017-015</td><td>Add 72 &amp;micro;l of sterile 5 M NaCl and aliquot into 50 &amp;micro;l</td></tr><tr><td>15 ml Conical tube</td><td>cell treat</td><td>229411</td><td></td></tr><tr><td>PBS CMF 10x</td><td>Gibco</td><td>14200</td><td>used at 1x, dilute with sterile Millipore filtered water</td></tr><tr><td>PBS 10x</td><td>Gibco</td><td>14080</td><td>used at 1x, dilute with sterile Millipore filtered water</td></tr><tr><td>Ham&#039;s F12</td><td>Lonza</td><td>12-615F</td><td></td></tr><tr><td>Fetal Bovine Serum Albumin (BSA)</td><td>Gibco</td><td>10438</td><td>use in F12HS20 at 10%</td></tr><tr><td>HEPES</td><td>Sigma</td><td>H3375</td><td>make sterile 1 M solution in distilled water, dilute in F12 media to obtain final concentration of 10 mM</td></tr><tr><td>Penicillin/streptomyocin</td><td>Sigma</td><td>P0781</td><td>use 5 ml in 500 ml of F12 media</td></tr><tr><td>NT3</td><td>Millipore</td><td>GF031</td><td>Add 1 ml of sterile Millipore water, aliquot under sterile conditions, store at -20 &amp;deg;C, use at final concentration of 10 ng/ml in F12H media, keep in -20 &amp;deg;C non-defrosting freezer</td></tr><tr><td>NGF</td><td>RnD systems</td><td>256-GF</td><td>Add 1 ml of sterile 1x PBS with 0.1% BSA, aliquot under sterile conditions, store at -20 &amp;deg;C, used at final concentration of 10 ng/ml in F12H media</td></tr><tr><td>L-Glutamine</td><td>Sigma</td><td>G7513</td><td>aliquot under sterile conditions, store at -20 &amp;deg;C, use at final concentration of 200 mM in F12H media</td></tr><tr><td>Trypsin</td><td>Sigma</td><td>T4049</td><td>aliquot under sterile conditions, store at -20 &amp;deg;C</td></tr><tr><td>Bovine Serum Albumin (BSA)</td><td>Gibco</td><td>15260</td><td></td></tr><tr><td colspan="4">Other items needed: general dissection instruments, including glass Pasteur pipettes, fertile white leghorn chicken eggs, check egg incubator (humidified, 37 &amp;deg;C), cell incubation chamber (humidified, 37 &amp;deg;C), laminar flow hood, binocular stereovision dissecting scope</td></tr><tr><td colspan="4">&lt;strong&gt;Immunocytochemistry Reagents Table&lt;/strong&gt;</td></tr><tr><td>Sucrose</td><td>Sigma</td><td>S9378</td><td>used in fixative solution (4% paraformaldehye, 30% sucrose, 2x PBS)</td></tr><tr><td>Triton-X 100</td><td>Sigma</td><td>T-8787</td><td></td></tr><tr><td>Paraformaldehyde</td><td>Sigma</td><td>P6148</td><td>used in fixative solution (4% paraformaldehye, 30% sucrose, 2x PBS)</td></tr><tr><td>Fluoromount G</td><td>Southern Biotech</td><td>0100-01</td><td></td></tr><tr><td>Normal goat serum</td><td>Life technologies</td><td>PCN500</td><td></td></tr><tr><td>Microscope slides</td><td>VWR</td><td>16004-430</td><td></td></tr><tr><td colspan="4">&lt;strong&gt;Primary Antibody Table&lt;/strong&gt;</td></tr><tr><td>Antibody against NCAM</td><td>Millipore</td><td>AB5032</td><td>polyclonal</td></tr><tr><td>Antibody against activated &amp;beta;1 ingegrin</td><td>Millipore</td><td>MAB19294</td><td>monoclonal</td></tr><tr><td colspan="4">&lt;strong&gt;Secondary Antibody Table&lt;/strong&gt;</td></tr><tr><td>Goat anti-mouse IgG Alexa 488</td><td>Life technologies</td><td>A11001</td><td></td></tr><tr><td>Goat anti-rabbit IgG Alexa 548</td><td>Life technologies</td><td>A11036</td><td></td></tr></tbody></table>

isolation and culture of dissociated sensory neurons from chick embryos

Neurons are multifaceted cells that carry information essential for a variety of functions including sensation, motor movement, learning, and memory. Studying neurons in vivo can be challenging due to their complexity, their varied and dynamic environments, and technical limitations. For these reasons, studying neurons in vitro can prove beneficial to unravel the complex mysteries of neurons. The well-defined nature of cell culture models provides detailed control over environmental conditions and variables. Here we describe how to isolate, dissociate, and culture primary neurons from chick embryos. This technique is rapid, inexpensive, and generates robustly growing sensory neurons. The procedure consistently produces cultures that are highly enriched for neurons and has very few non-neuronal cells (less than 5%). Primary neurons do not adhere well to untreated glass or tissue culture plastic, therefore detailed procedures to create two distinct, well-defined laminin-containing substrata for neuronal plating are described. Cultured neurons are highly amenable to multiple cellular and molecular techniques, including co-immunoprecipitation, live cell imagining, RNAi, and immunocytochemistry. Procedures for double immunocytochemistry on these cultured neurons have been optimized and described here.

The protocol described here enables investigators to culture an enriched population of dissociated embryonic sensory neurons with very few (e.g., &#60;5%) non-neuronal cells7,8,10,16. Numerous DRGs can be obtained from the lumbosacral, thoracic and cervical regions. Depending upon the needs of the investigator, DRGs from these distinct anatomical regions can be easily isolated. For example, Figure 1 shows images of the chick embryo through various stages of dissection with the lumbar ...

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Isolation and Culture of Dissociated Sensory Neurons From Chick Embryos

Cell culture models provide detailed control over environmental conditions and thus provide a powerful platform to elucidate numerous aspects of neuronal cell biology. We describe a rapid, inexpensive, and reliable method to isolate, dissociate, and culture sensory neurons from chick embryos. Details of substrata preparation and immunocytochemistry are also provided.

Neurons are multifaceted cells that carry information essential for a variety of functions including sensation, motor movement, learning, and memory. ...

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Neuroscience

14.3K Views.  Assumption College. Cell culture models provide detailed control over environmental conditions and thus provide a powerful platform to elucidate numerous aspects of neuronal cell biology. We describe a rapid, inexpensive, and reliable method to isolate, dissociate, and culture sensory neurons from chick embryos. Details of substrata preparation and immunocytochemistry are also provided.

Video: Isolation and Culture of Dissociated Sensory Neurons From Chick Embryos

Dissection and Culture of Chick Statoacoustic Ganglion and Spinal Cord Explants in Collagen Gels for Neurite Outgrowth Assays

The sensory organs of the chicken inner ear are innervated by the peripheral processes of statoacoustic ganglion (SAG) neurons. Sensory organ innervation depends on a combination of axon guidance cues1 and survival factors2 located along the trajectory of growing axons and/or within their sensory organ targets. For example, functional interference with a classic axon guidance signaling pathway, semaphorin-neuropilin, generated misrouting of otic axons3. Also, several growth factors expressed in the sensory targets of the inner ear, including Neurotrophin-3 (NT-3) and Brain Derived Neurotrophic Factor (BDNF), have been manipulated in transgenic animals, again leading to misrouting of SAG axons4. These same molecules promote both survival and neurite outgrowth of chick SAG neurons in vitro5,6.
Here, we describe and demonstrate the in vitro method we are currently using to test the responsiveness of chick SAG neurites to soluble proteins, including known morphogens such as the Wnts, as well as growth factors that are important for promoting SAG neurite outgrowth and neuron survival. Using this model system, we hope to draw conclusions about the effects that secreted ligands can exert on SAG neuron survival and neurite outgrowth. 
SAG explants are dissected on embryonic day 4 (E4) and cultured in three-dimensional collagen gels under serum-free conditions for 24 hours. First, neurite responsiveness is tested by culturing explants with protein-supplemented medium. Then, to ask whether point sources of secreted ligands can have directional effects on neurite outgrowth, explants are co-cultured with protein-coated beads and assayed for the ability of the bead to locally promote or inhibit outgrowth. We also include a demonstration of the dissection (modified protocol7) and culture of E6 spinal cord explants. We routinely use spinal cord explants to confirm bioactivity of the proteins and protein-soaked beads, and to verify species cross-reactivity with chick tissue, under the same culture conditions as SAG explants. These in vitro assays are convenient for quickly screening for molecules that exert trophic (survival) or tropic (directional) effects on SAG neurons, especially before performing studies in vivo. Moreover, this method permits the testing of individual molecules under serum-free conditions, with high neuron survival8.

We demonstrate how to dissect and culture chick E4 statoacoustic ganglion and E6 spinal cord explants. Explants are cultured under serum-free conditions in 3D collagen gels for 24 hours. Neurite responsiveness is tested with growth factor-supplemented medium and with protein-coated beads.

The sensory organs of the chicken inner ear are innervated by the peripheral processes of statoacoustic ganglion (SAG) neurons. Sensory organ innervation ...

Isolation and Culture of Rat Embryonic Neural Cells: A Quick Protocol

We are describing a quick method to dissociate and culture hippocampal or cortical neurons from E15-17 rat embryos. The procedure can be applied successfully to the isolation of mouse and human primary neurons and neural progenitors. Dissociated neurons are maintained in serum-free medium up to several weeks. These cultures can be used for nucleofection, immunocytochemistry, nucleic acids preparation, as well as electrophysiology. Older neuronal cultures can also be transfected with a good efficiency rate by lentiviral transduction and, less efficiently, with calcium phosphate or lipid-based methods such as lipofectamine.

We describe a rapid methodology to isolate and culture hippocampal and cortical neurons from rodent embryos. This protocol allows us to perform experiments in which nearly pure neuronal cultures are required.

We are describing a quick method to dissociate and culture hippocampal or cortical neurons from E15-17 rat embryos. The procedure can be applied ...

Chicken Embryo Spinal Cord Slice Culture Protocol

Slice cultures can facilitate the manipulation of embryo development both pharmacologically and through gene manipulations. In this reduced system, potential lethal side effects due to systemic drug applications can be overcome. However, culture conditions must ensure that normal development proceeds within the reduced environment of the slice. We have focused on the development of the spinal cord, particularly that of spinal motor neurons. We systematically varied culture conditions of chicken embryo slices from the point at which most spinal motor neurons had been born. We assayed the number and type of motor neurons that survived during the culture period and the position of those motor neurons compared to that in vivo. We found that serum type and neurotrophic factors were required during the culture period and were able to keep motor neurons alive for at least 24 hr and allow those motor neurons to migrate to appropriate positions in the spinal cord. We present these culture conditions and the methodology of preparing the embryo slice cultures using eviscerated chicken embryos embedded in agarose and sliced using a vibratome.

Slice cultures facilitate the manipulation of embryo development by gene and pharmacological perturbations. However, culture conditions must ensure that normal development can proceed within the reduced environment of the slice. We illustrate a protocol that facilitates normal spinal cord development to proceed for at least 24 hr.

Slice cultures can facilitate the manipulation of  embryo development both pharmacologically and through gene manipulations. In  this reduced system, ...

Isolation of Sensory Neurons of Aplysia californica for Patch Clamp Recordings of Glutamatergic Currents

The marine gastropod mollusk Aplysia californica has a venerable history as a model of nervous system function, with particular significance in studies of learning and memory. The typical preparations for such studies are ones in which the sensory and motoneurons are left intact in a minimally dissected animal, or a technically elaborate neuronal co-culture of individual sensory and motoneurons. Less common is the isolated neuronal preparation in which small clusters of nominally homogeneous neurons are dissociated into single cells in short term culture. Such isolated cells are useful for the biophysical characterization of ion currents using patch clamp techniques, and targeted modulation of these conductances. A protocol for preparing such cultures is described. The protocol takes advantage of the easily identifiable glutamatergic sensory neurons of the pleural and buccal ganglia, and describes their dissociation and minimal maintenance in culture for several days without serum.

Isolation of Sensory Neurons of Aplysia californica for Patch Clamp Recordings of Glutamatergic Currents

We describe the dissection of the nervous system of the marine sea hare Aplysia after anesthesia, the isolation of neurons for short term-tissue culture, and recordings of single cell ion currents via the patch clamp technique.

The marine gastropod mollusk Aplysia californica has a venerable  history as a model of nervous system function, with particular significance in  studies ...

Isolation and Culture of Chick Ciliary Ganglion Neurons

Chick ciliary ganglia (CG) are part of the parasympathetic nervous system and are responsible for the innervation of the muscle tissues present in the eye. This ganglion is constituted by a homogenous population of ciliary and choroidal neurons that innervate striated and smooth muscle fibers, respectively. Each of these neuronal types regulate specific eye structures and functions. Over the years, neuronal cultures of the chick ciliary ganglia were shown to be effective cell models in the study of muscle-nervous system interactions, which communicate through cholinergic synapses. Ciliary ganglion neurons are, in its majority, cholinergic. This cell model has been shown to be useful comparatively to previously used heterogeneous cell models that comprise several neuronal types, besides cholinergic. Anatomically, the ciliary ganglion is localized between the optic nerve (ON) and the choroid fissure (CF). Here, we describe a detailed procedure for the dissection, dissociation and in vitro culture of ciliary ganglia neurons from chick embryos. We provide a step-by-step protocol in order to obtain highly pure and stable cellular cultures of CG neurons, highlighting key steps of the process. These cultures can be maintained in vitro for 15 days and, hereby, we show the normal development of CG cultures. The results also show that these neurons can interact with muscle fibers through neuro-muscular cholinergic synapses.

Chick ciliary ganglia (CG) are part of the parasympathetic nervous system. Neuronal cultures of chick CG neurons were shown to be effective cell models in the study of nerve muscle interactions. We describe a detailed protocol for the dissection, dissociation and in vitro culture of CG neurons from chick embryos.

Chick ciliary ganglia (CG) are part of the parasympathetic nervous system and are responsible for the innervation of the muscle tissues present in the ...

Isolation of DRG Neurons and Coculture with Schwann Cell Precursors to Generate Schwann Cells

Source: Tsui, Y, et al. <a href="https://app.jove.com/v/55794">Hypoxic Preconditioning of Marrow-derived Progenitor Cells as a Source for the Generation of Mature Schwann Cells.</a> J. Vis. Exp. (2017).
This video demonstrates a procedure for isolating dorsal root ganglion (DRG) neurons from rat embryos and co-culturing them with Schwann cell precursors to generate mature Schwann cells. The isolated DRGs are processed to isolate neurons and glial cells. The isolated cells are cultured to purify the neurons, which are then co-cultured with Schwann cell-like cells (SCLCs) in a co-culture medium. Interaction with the DRG neurons leads to the maturation of SCLCs into Schwann cells.

Generation of Fate-committed Schwann Cells via Coculture with DRG Neurons
1. Preparation of purified rat DRG neurons

	Autoclave all dissection tools ...

JoVE Encyclopedia of Experiments

Neuronal Culture Techniques

Co-culture and Interaction Studies

Isolation of Cells from Sensory Ganglia

Source: Kaelberer, M. M., et al. <a href="https://app.jove.com/v/53917">A Method to Target and Isolate Airway-innervating Sensory Neurons in Mice.</a> J. Vis. Exp. (2016).
This video demonstrates the isolation of cells from the sensory ganglia of mice. Ganglia are subjected to enzymatic digestion to dissolve the extracellular matrix. Single cells are then collected via filtering through a cell strainer followed by density gradient centrifugation for debris removal. Finally, washing and centrifugation are done to collect the isolated cells for future analysis.

All procedures involving sample collection have been performed in accordance with the institute&#8217;s IRB guidelines.
1. Sensory Ganglia Dissociation

	...

Primary Neuronal Culture

Isolation and Culturing of Cells from Mouse Embryo Dorsolateral Telencephalons

Source: Landeira, B. S., et al. <a href="https://app.jove.com/v/56063">Live Imaging of Primary Cerebral Cortex Cells Using a 2D Culture System.</a> J. Vis. Exp. (2017)
This video demonstrates a protocol for isolating and culturing primary cerebral cortex cells from the dorsolateral telencephalon of mouse embryos.

All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.
1. ...

Isolating Cranial Neural Folds From a Chick Embryo for a Neural Crest Cell Culture

Source: Jacques-Fricke, B. T., et al. <a href="https://app.jove.com/v/63799">Preparation and Morphological Analysis of Chick Cranial Neural Crest Cell Cultures.</a> J. Vis. Exp. (2022).
This video illustrates a technique for isolating cranial neural folds from the midbrain region of chick embryos. It presents a detailed dissection process of the neural folds, their placement, and attachment on fibronectin-coated coverslips, followed by the observation of neural crest cell migration from the neural folds.

Advanced Neuronal Models

Isolating and Culturing Chick Embryonic Neurons on a Multi-Electrode Array

Source: Sanchez, K. R., et al., <a href="https://app.jove.com/v/56300">Assessment of the Effects of Endocrine Disrupting Compounds on the Development of Vertebrate Neural Network Function Using Multi-electrode Arrays.</a> J. Vis. Exp.(2018)
This video demonstrates a method to isolate neurons from the forebrain of an early-stage chick embryo and culture them on a microelectrode array to form a neuronal network.

Isolation and Culture of Dissociated Sensory Neurons From Chick Embryos

Summary

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Chapters in this video

Dissection and Culture of Chick Statoacoustic Ganglion and Spinal Cord Explants in Collagen Gels for Neurite Outgrowth Assays

Isolation and Culture of Rat Embryonic Neural Cells: A Quick Protocol

Chicken Embryo Spinal Cord Slice Culture Protocol

Isolation of Sensory Neurons of Aplysia californica for Patch Clamp Recordings of Glutamatergic Currents

Isolation and Culture of Chick Ciliary Ganglion Neurons

Isolation of DRG Neurons and Coculture with Schwann Cell Precursors to Generate Schwann Cells

Isolation of Cells from Sensory Ganglia

Isolation and Culturing of Cells from Mouse Embryo Dorsolateral Telencephalons

Isolating Cranial Neural Folds From a Chick Embryo for a Neural Crest Cell Culture

Isolating and Culturing Chick Embryonic Neurons on a Multi-Electrode Array