Name: A Procedure for Mouse Dorsal Root Ganglion Cryosectioning (Video) | JoVE Journal
Uploaded: 2023-06-09T13:50:00.000+00:00
Duration: 4 min 20 s
Description: Learn a reliable cryostat sectioning method for mouse dorsal root ganglion tissue to obtain high-quality, flat cross-sections. This protocol enables precise immunohistochemistry studies in neuroscience research.

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5 minutes

For the present study, the animal experiments were approved by UCSF Institutional Animal Care and Use Committee and were conducted in accordance with the NIH Guide for the Care and Use of Laboratory animals. Adult, 8-12-week-old C57BL/6 male and female mice (in-house bred) were used here.
1. DRG sample preparation
<ol>
	<li>Anesthetize the mice with 2.5% Avertin (see Table of Materials). Ensure adequate anesthesia by the lack of response to painful stimulation. Perfuse the animals transcardially with 1x phosphate-buffered saline (PBS) followed by 4% formaldehyde, as previously described14,15,16.</li>
	<li>Dissect DRG tissue from the spinal cord, as previously described14,15,16.</li>
	<li>Post-fix the dissected DRGs in 4% formaldehyde for 3 h at room temperature.</li>
	<li>Put the DRGs in 30% sucrose in PBS at 4 &#176;C overnight.</li>
	<li>Preparing the base optimal cutting temperature (OCT)
	<ol>
		<li>Add the OCT compound (see Table of Materials) to cover the top surface of the aluminum block and freeze at -20 &#176;C for 5-10 min (Figure 1A).</li>
		<li>Cut off the top of the OCT using the cryostat (see Table of Materials) at 30 &#181;m thickness until its surface is flat as the base OCT (Figure 1B).</li>
		<li>Make a mark at the bottom (six o&#39;clock position) of the base OCT to mark its orientation, before taking the aluminum block off the cryostat (Figure 1C).</li>
		<li>In the following steps, keep the mark at the six o&#39;clock position to maintain the same orientation, which can lead to obtaining more sections of the DRG sample. 
		NOTE: If the orientation is lost and the DRG sample is cut at a different angle, the DRG sample cannot be cut completely from top to bottom, which will leave some samples left out on the base OCT and wasted, as the base OCT will be encountered while trying to cut the DRG sample (Figure 1C).</li>
	</ol>
	</li>
	<li>Performing OCT embedment of DRGs
	<ol>
		<li>Dry the DRG tissue before putting it on the OCT.
		<ol>
			<li>Before adding the DRG onto the block, ensure to remove the 30% sucrose/PBS solution around the sample.</li>
			<li>Dry the DRG sample by placing it on a dry Petri dish (Figure 2A) and moving it from one location to another two or three times with dry tweezers (Figure 2B).</li>
			<li>Dry the tweezers with lint-free tissue before moving another DRG sample (Figure 2C).</li>
		</ol>
		</li>
		<li>Put the dry DRG onto the base OCT.
		<ol>
			<li>With dry tweezers, place the dry DRG onto the base OCT at the 12 o&#39;clock position (Figure 1D).</li>
			<li>Keep at least 5 mm between the upper edge of the DRG and the upper edge of the base OCT.</li>
			<li>Put the dorsal part of the DRG at the 12 o&#39;clock position and the ventral part at the six o&#39;clock position (Figure 1D).</li>
		</ol>
		</li>
		<li>Embed the DRG tissue with OCT.
		<ol>
			<li>Add more OCT to cover the entire DRG sample in a round or oval shape, with the DRG in the center (Figure 1E).</li>
			<li>Ensure the upper edge of the OCT covers the DRG at the upper edge of the base OCT (Figure 1F), as this makes it easier to transfer the section onto the glass slide (Figure 3A). 
			NOTE: If the cover OCT is in the middle of the base OCT, the upper edge of the base OCT will block the glass slide to collect the section (Figure 3B).</li>
			<li>Freeze the cover OCT and DRG sample at -20 &#176;C for another 5 min (Figure 1G). Do not trim the OCT around the DRG sample.</li>
			<li>Cut off the top of the cover OCT at a 30 &#181;m thickness until the DRG is visible.</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>
2. Cryosectioning of the DRG
<ol>
	<li>Change the cryostat section thickness to 12 &#181;m to cut DRG sections onto the slide (Figure 1H).</li>
	<li>Hold the OCT section at the bottom with a small paintbrush cooled to -20 &#176;C. 
	NOTE: It is important not to cut the whole section completely, but to leave 1-3 mm uncut (Figure 1I).</li>
	<li>Use the end of a room-temperature tweezer to gently touch the bottom (six o&#39;clock position) of the section so that it sticks to the platform surface (Figure 1J). This prevents the section from curving back in a roll, which makes it difficult to collect the section on the slide. 
	NOTE: When the bottom of the section sticks to the platform surface, and the top of the section still connects with the cover OCT, the section is in a flat shape (Figure 1K), making it much easier to collect the section on the slide.</li>
	<li>Take a charged glass slide (see Table of Materials) and slowly place the slide over the section. As soon as the section starts to stick to the slide, gently pull the slide backward (Figure 1L).</li>
	<li>Follow the same process to get more DRG sections onto the slide without overlapping the sections (Figure 1M). Ensure that a new DRG section is not placed over the OCT of another DRG section (Figure 4), as such a section cannot stay well on the slide and can be washed away during the immunochemistry staining process.</li>
</ol>
3. Nissl staining of the DRG section on the glass slide
<ol>
	<li>Wash the sections for 10 min in PBS plus 0.1% Triton X-10. Then, wash the sections twice with PBS.</li>
	<li>Apply a 1:300 Nissl stain (see Table of Materials) to the slide and incubate for 20 min at room temperature.</li>
	<li>Wash the section with PBS plus 0.1% Triton X-100. Then, wash the sections twice with PBS for 5 min, and then for 2 h at room temperature.</li>
	<li>Apply 4&#8242;,6-diamidino-2-phenylindole (DAPI) fluoromount-G (see Table of Materials) to cover the sections with a coverslip.</li>
</ol>

Mouse Dorsal Root Ganglion Cryosectioning

<ol><li>Guan, Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Injured+sensory+neuron-derived+CSF1+induces+microglial+proliferation+and+DAP12-dependent+pain%5BTitle%5D)+AND+%22Nature+Neuroscience%22%5BJournal%5D)">Injured sensory neuron-derived CSF1 induces microglial proliferation and DAP12-dependent pain.</a> Nature Neuroscience. 19 (1), 94-101 (2016).</li>
<li>Yu, X., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Dorsal+root+ganglion+macrophages+contribute+to+both+the+initiation+and+persistence+of+neuropathic+pain%5BTitle%5D)+AND+%22Nature+Communications%22%5BJournal%5D)">Dorsal root ganglion macrophages contribute to both the initiation and persistence of neuropathic pain.</a> Nature Communications. 11 (1), 264(2020).</li>
<li>Costa, F. A. L., Moreira Neto, F. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Satellite+glial+cells+in+sensory+ganglia%3A+its+role+in+pain%5BTitle%5D)+AND+%22Brazilian+Journal+of+Anesthesiology%22%5BJournal%5D)">Satellite glial cells in sensory ganglia: its role in pain.</a> Brazilian Journal of Anesthesiology. 65 (1), 73-81 (2015).</li>
<li>Noguri, T., Hatakeyama, D., Kitahashi, T., Oka, K., Ito, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Profile+of+dorsal+root+ganglion+neurons%3A+study+of+oxytocin+expression%5BTitle%5D)+AND+%22Molecular+Brain%22%5BJournal%5D)">Profile of dorsal root ganglion neurons: study of oxytocin expression.</a> Molecular Brain. 15 (1), 44(2022).</li>
<li>Su, P. P., Zhang, L., He, L., Zhao, N., Guan, Z. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+role+of+neuro-immune+interactions+in+chronic+pain%3A+implications+for+clinical+practice%5BTitle%5D)+AND+%22Journal+of+Pain+Research%22%5BJournal%5D)">The role of neuro-immune interactions in chronic pain: implications for clinical practice.</a> Journal of Pain Research. 15, 2223-2248 (2022).</li>
<li>Esposito, M. F., Malayil, R., Hanes, M., Deer, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Unique+characteristics+of+the+dorsal+root+ganglion+as+a+target+for+neuromodulation%5BTitle%5D)+AND+%22Pain+Medicine%22%5BJournal%5D)">Unique characteristics of the dorsal root ganglion as a target for neuromodulation.</a> Pain Medicine. 20, S23-S30 (2019).</li>
<li>Chen, X. J., Sun, Y. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Central+circuit+mechanisms+of+itch%5BTitle%5D)+AND+%22Nature+Communications%22%5BJournal%5D)">Central circuit mechanisms of itch.</a> Nature Communications. 11 (1), 3052(2020).</li>
<li>Guan, Z., Hellman, J., Schumacher, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Contemporary+views+on+inflammatory+pain+mechanisms%3A+TRPing+over+innate+and+microglial+pathways%5BTitle%5D)+AND+%22F1000Research%22%5BJournal%5D)">Contemporary views on inflammatory pain mechanisms: TRPing over innate and microglial pathways.</a> F1000Research. , (2016).</li>
<li>Boadas-Vaello, P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Neuroplasticity+of+ascending+and+descending+pathways+after+somatosensory+system+injury%3A+reviewing+knowledge+to+identify+neuropathic+pain+therapeutic+targets%5BTitle%5D)+AND+%22Spinal+Cord%22%5BJournal%5D)">Neuroplasticity of ascending and descending pathways after somatosensory system injury: reviewing knowledge to identify neuropathic pain therapeutic targets.</a> Spinal Cord. 54 (5), 330-340 (2016).</li>
<li>Guha, D., Shamji, M. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+dorsal+root+ganglion+in+the+pathogenesis+of+chronic+neuropathic+pain%5BTitle%5D)+AND+%22Neurosurgery%22%5BJournal%5D)">The dorsal root ganglion in the pathogenesis of chronic neuropathic pain.</a> Neurosurgery. 63, 118-126 (2016).</li>
<li>Shorrock, H. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((UBA1%2FGARS-dependent+pathways+drive+sensory-motor+connectivity+defects+in+spinal+muscular+atrophy%5BTitle%5D)+AND+%22Brain%22%5BJournal%5D)">UBA1/GARS-dependent pathways drive sensory-motor connectivity defects in spinal muscular atrophy.</a> Brain. 141 (10), 2878-2894 (2018).</li>
<li>Sleigh, J. N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Trk+receptor+signaling+and+sensory+neuron+fate+are+perturbed+in+human+neuropathy+caused+by+Gars+mutations%5BTitle%5D)+AND+%22Proceedings+of+the+National+Academy+of+Sciences%22%5BJournal%5D)">Trk receptor signaling and sensory neuron fate are perturbed in human neuropathy caused by Gars mutations.</a> Proceedings of the National Academy of Sciences. 114 (16), E3324-E3333 (2017).</li>
<li>Rubio, M. A., Herrando-Grabulosa, M., Gaja-Capdevila, N., Vilches, J. J., Navarro, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Characterization+of+somatosensory+neuron+involvement+in+the+SOD1%28G93A%29+mouse+model%5BTitle%5D)+AND+%22Scientific+Reports%22%5BJournal%5D)">Characterization of somatosensory neuron involvement in the SOD1(G93A) mouse model.</a> Scientific Reports. 12 (1), 7600(2022).</li>
<li>Sleigh, J. N., West, S. J., Schiavo, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((A+video+protocol+for+rapid+dissection+of+mouse+dorsal+root+ganglia+from+defined+spinal+levels%5BTitle%5D)+AND+%22BMC+Research+Notes%22%5BJournal%5D)">A video protocol for rapid dissection of mouse dorsal root ganglia from defined spinal levels.</a> BMC Research Notes. 13 (1), 302(2020).</li>
<li>Sleigh, J. N., Weir, G. A., Schiavo, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((A+simple%2C+step-by-step+dissection+protocol+for+the+rapid+isolation+of+mouse+dorsal+root+ganglia%5BTitle%5D)+AND+%22BMC+Research+Notes%22%5BJournal%5D)">A simple, step-by-step dissection protocol for the rapid isolation of mouse dorsal root ganglia.</a> BMC Research Notes. 9, 82(2016).</li>
<li>Perner, C., Sokol, C. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Protocol+for+dissection+and+culture+of+murine+dorsal+root+ganglia+neurons+to+study+neuropeptide+release%5BTitle%5D)+AND+%22STAR+Protocols%22%5BJournal%5D)">Protocol for dissection and culture of murine dorsal root ganglia neurons to study neuropeptide release.</a> STAR Protocols. 2 (1), 100333(2021).</li>
<li>Haberberger, R. V., Barry, C., Matusica, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Immortalized+dorsal+root+ganglion+neuron+cell+lines%5BTitle%5D)+AND+%22Frontiers+in+Cellular+Neuroscience%22%5BJournal%5D)">Immortalized dorsal root ganglion neuron cell lines.</a> Frontiers in Cellular Neuroscience. 14, 184(2020).</li>
<li>Pokhilko, A., Nash, A., Cader, M. Z. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Common+transcriptional+signatures+of+neuropathic+pain%5BTitle%5D)+AND+%22Pain%22%5BJournal%5D)">Common transcriptional signatures of neuropathic pain.</a> Pain. 161 (7), 1542-1554 (2020).</li>
<li>Martin, S. L., Reid, A. J., Verkhratsky, A., Magnaghi, V., Faroni, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Gene+expression+changes+in+dorsal+root+ganglia+following+peripheral+nerve+injury%3A+roles+in+inflammation%2C+cell+death+and+nociception%5BTitle%5D)+AND+%22Neural+Regeneration+Research%22%5BJournal%5D)">Gene expression changes in dorsal root ganglia following peripheral nerve injury: roles in inflammation, cell death and nociception.</a> Neural Regeneration Research. 14 (6), 939-947 (2019).</li>
<li>Miller, R. J., Jung, H., Bhangoo, S. K., White, F. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Cytokine+and+chemokine+regulation+of+sensory+neuron+function%5BTitle%5D)+AND+%22Handbook+of+Experimental+Pharmacology%22%5BJournal%5D)">Cytokine and chemokine regulation of sensory neuron function.</a> Handbook of Experimental Pharmacology. (194), 417-449 (2009).</li>
<li>Neto, E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Axonal+outgrowth%2C+neuropeptides+expression+and+receptors+tyrosine+kinase+phosphorylation+in+3D+organotypic+cultures+of+adult+dorsal+root+ganglia%5BTitle%5D)+AND+%22PLoS+One%22%5BJournal%5D)">Axonal outgrowth, neuropeptides expression and receptors tyrosine kinase phosphorylation in 3D organotypic cultures of adult dorsal root ganglia.</a> PLoS One. 12 (7), e0181612(2017).</li>
<li>Nascimento, A. I., Mar, F. M., Sousa, M. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+intriguing+nature+of+dorsal+root+ganglion+neurons%3A+Linking+structure+with+polarity+and+function%5BTitle%5D)+AND+%22Progress+in+Neurobiolology%22%5BJournal%5D)">The intriguing nature of dorsal root ganglion neurons: Linking structure with polarity and function.</a> Progress in Neurobiolology. 168, 86-103 (2018).</li>
<li>Middleton, S. J., Perez-Sanchez, J., Dawes, J. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+structure+of+sensory+afferent+compartments+in+health+and+disease%5BTitle%5D)+AND+%22Journal+of+Anatomy%22%5BJournal%5D)">The structure of sensory afferent compartments in health and disease.</a> Journal of Anatomy. 241 (5), 1186-1210 (2022).</li>
<li>Nguyen, M. Q., von Buchholtz, L. J., Reker, A. N., Ryba, N. J., Davidson, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Single-nucleus+transcriptomic+analysis+of+human+dorsal+root+ganglion+neurons%5BTitle%5D)+AND+%22eLife%22%5BJournal%5D)">Single-nucleus transcriptomic analysis of human dorsal root ganglion neurons.</a> eLife. 10, e71752(2021).</li>
<li>Usoskin, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Unbiased+classification+of+sensory+neuron+types+by+large-scale+single-cell+RNA+sequencing%5BTitle%5D)+AND+%22Nature+Neuroscience%22%5BJournal%5D)">Unbiased classification of sensory neuron types by large-scale single-cell RNA sequencing.</a> Nature Neuroscience. 18 (1), 145-153 (2015).</li>
<li>Hunt, M. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((DRGquant%3A+A+new+modular+AI-based+pipeline+for+3D+analysis+of+the+DRG%5BTitle%5D)+AND+%22Journal+of+Neuroscience+Methods%22%5BJournal%5D)">DRGquant: A new modular AI-based pipeline for 3D analysis of the DRG.</a> Journal of Neuroscience Methods. 371, 109497(2022).</li>
</ol>

The authors have nothing to disclose.

This protocol provides an easy step-by-step procedure for cryostat sectioning of the mouse DRG to obtain high-quality DRG sections on slides reliably.There are four critical steps in this protocol. First, the DRG sample and the tweezers must be dry before putting the DRG sample onto the base OCT. Any liquid surrounding the DRG sample will form an ice shell around it, resulting in DRG sections separating from the OCT and curving up. Second, if the aluminum block does not have a mark, or if the base OCT covers the mark, it...

The dorsal root ganglion (DRG) contains the primary sensory neurons, the tissue macrophages, and the satellite cells that surround the primary sensory neurons1,2,3,4. It is a key anatomic structure in processing innocuous and noxious signals, and plays critical roles in pain, itch, and various peripheral nerve disorders5,6,7,8,9,10,11,12,13. Although several methods have been developed to dissect DRG tissue from the mouse spinal cord14,15,16, cryosectioning of the DRG tissue remains challenging as the DRG tissue is quite small, and cryostat sections of DRG samples tend to curve into rolls, making it difficult to properly transfer the cryostat sections onto glass slides. However, proper cryosectioning of the DRG tissue is crucial for immunohistochemistry studies and the structure of DRG sensory neurons17,18,19,20,21,22,23. Moreover, as single-cell RNA sequencing results have revealed the remarkable heterogeneity of DRG sensory neurons in both humans24 and mice25, proper cryosectioning of DRG tissue is critical for investigating the functional role of different DRG cells in various physiological and pathological conditions.
Although the tissue-clearing technique has been applied to investigate the 3D reconstruction of the DRG26 as an alternative technique of cryosectioning the DRG, the tissue-clearing technique is time- and labor-consuming. In comparison, cryosectioning of the DRG is quick and relatively easy to perform, and thus it remains to be a key technique for immunohistochemistry and structure studies of the DRG and other regions of the central nervous system. However, obtaining high-quality, intact, and flat cryostat sections onto glass slides remains to be a challenge in neuroscience research because of the tiny sample size of tissues, like the DRG and certain brain regions, and there is no article describing the optimal protocol at this point for cryosectioning small-sized tissue samples, such as mouse DRGs.
This protocol provides an easy, step-by-step technique for cryostat sectioning of the mouse DRG to reliably obtain as many high-quality DRG sections on the slides for subsequent DRG studies. While specifically designed for cryosectioning DRG samples, this technique can potentially be used for cryosectioning various other tissues with a small sample size.

<table><tbody><tr><td>Avertin</td><td>Sigma-Aldrich</td><td>T48402-25G</td><td>Anesthetize animal</td></tr><tr><td>Epredia&amp;nbsp;Cryotome Cryostat Cryocassettes, 25 mm dia. Crosshatched</td><td>Fisherbrand</td><td>1910</td><td>Hold the OCT section at the bottom&amp;nbsp;</td></tr><tr><td>Ergo Tweezers</td><td>Fisherbrand</td><td>S95310</td><td>Using the end of a tweezer to gently touch the bottom (6 o&amp;rsquo;clock) of the section so that it sticks to the platform surface to prevent the section from curving back in a roll&amp;nbsp;</td></tr><tr><td>Fisherbrand&amp;nbsp;Superfrost Plus Microscope Slides</td><td>Fisherbrand</td><td>1255015</td><td>To collect the DRG section&amp;nbsp;</td></tr><tr><td>Marking pens</td><td>Fisherbrand</td><td>133794</td><td>&amp;nbsp;Mark the orientation of base OCT</td></tr><tr><td>Scigen&amp;nbsp;Tissue-Plus O.C.T. Compound</td><td>Fisherbrand</td><td>&amp;nbsp;23730571</td><td>Embedding medium for frozen tissue specimens to ensure optimal cutting temperature (O.C.T.).</td></tr></tbody></table>

a procedure for mouse dorsal root ganglion cryosectioning

A Procedure for Mouse Dorsal Root Ganglion Cryosectioning

High-quality mouse dorsal root ganglion (DRG) cryostat sections are crucial for proper immunochemistry staining and RNAscope studies in the research of inflammatory and neuropathic pain, itch, as well as other peripheral neurological conditions. However, it remains a challenge to consistently obtain high-quality, intact, and flat cryostat sections onto glass slides because of the tiny sample size of the DRG tissue. So far, there is no article describing an optimal protocol for DRG cryosectioning. This protocol presents a step-by-step method to resolve the frequently encountered difficulties associated with DRG cryosectioning. The presented article explains how to remove the surrounding liquid from the DRG tissue samples, place the DRG sections on the slide facing the same orientation, and flatten the sections on the glass slide without curving up. Although this protocol has been developed for cryosectioning the DRG samples, it can be applied for the cryosectioning of many other tissues with a small sample size.

The current study collected about 16 continuous, high-quality DRG sections from one mouse L4 DRG. The obtained sections were without any distortion. Figure 1 depicts the step-by-step procedure for the cryosectioning. The removal of extra liquid from the tissue sections is shown in Figure 2. The process of OCT embedment of the tissues is highlighted in Figure 3. Figure 4 shows the proper placement of the...

Presented here is the development for consistently acquiring high-quality dorsal root ganglion cryostat sections.

High-quality mouse dorsal root ganglion (DRG) cryostat sections are crucial for proper immunochemistry staining and RNAscope studies in the research of ...

a-procedure-for-mouse-dorsal-root-ganglion-cryosectioning

Research

JoVE Journal

Neuroscience

We present a method for chromatin immunoprecipitation from dorsal root ganglia tissue following axonal injury. The approach can be used to identify specific transcription factor binding sites and epigenetic modification of histone and DNA important for the regeneration of injured axons in both the peripheral and central nervous system.

Chromatin Immunoprecipitation from Dorsal Root Ganglia Tissue following Axonal Injury

This video demonstrates an enzyme-free protocol to isolate macrophages from mouse dorsal root ganglion (DRG) using a mechanical dissociation technique. Upon homogenization of the freshly collected DRG tissue, antibodies against the cell-surface receptors on the macrophages are used to label the cells fluorescently, followed by performing flow cytometry to confirm the presence of macrophages in the sample.

Isolation of Macrophages from Mouse Dorsal Root Ganglion Using Mechanical Dissociation

This video demonstrates a method for harvesting neurons from the dorsal root ganglia (DRG). DRG from a rat's spinal column is isolated, treated with enzymes, and then mechanically dissociated to obtain a single-cell suspension. The neurons are separated from glial cells using density gradient centrifugation and cultured in a growth medium.

A Technique for Harvesting and Dissociating Dorsal Root Ganglia for Neuronal Cultures

Here, we present a protocol for hydraulic extrusion of the spinal cord as well as identification and isolation of specific dorsal root ganglia (DRGs) in the same rodent. Compared to standard spinal cord isolation methods, this method is significantly faster and reduces the risk of tissue damage.

Hydraulic Extrusion of the Spinal Cord and Isolation of Dorsal Root Ganglia in Rodents

Here we present a mechanical dissociation protocol to rapidly isolate macrophages from the dorsal root ganglion for phenotyping and functional analysis.

Rapid Isolation of Dorsal Root Ganglion Macrophages

A convenient gravity-fed perfusion method for histological analysis of the mouse central nervous system is presented. Immunofluorescent detection of phosphorylated α-synuclein is demonstrated in a mouse model of Parkinson's disease. This work also comprehensively describes the transcardial perfusion, dissection, tissue freezing/embedding, and frozen sectioning steps.

A Gravity-Fed Transcardial Perfusion Method for Histologic Analysis of the Mouse Central Nervous System

This paper describes an immunopanning protocol for adult mouse dorsal root ganglia. By adhering antibodies to culture plates, we can negatively select and remove non-neuronal cells. We show that the cultures are enriched for neurons using this protocol, allowing for an in-depth study of neuronal responses to manipulation.

Enrichment of Adult Mouse Dorsal Root Ganglia Neuron Cultures by Immunopanning

This protocol describes the surgical exposure of the dorsal root ganglion (DRG) followed by GCaMP3 (genetically-encoded Ca2+ indicator; Green Fluorescent Protein-Calmodulin-M13 Protein 3) Ca2+ imaging of the neuronal ensembles using Pirt-GCaMP3 mice while applying a variety of stimuli to the ipsilateral hind paw.

In Vivo Calcium Imaging of Neuronal Ensembles in Networks of Primary Sensory Neurons in Intact Dorsal Root Ganglia

This article presents a manipulation for treating chronic compression of the dorsal root ganglion in rats using Tuina therapy, along with a method for evaluating its effectiveness based on pain behavior and histopathological results.

Analgesic Effect of Tuina on Rat Models with Compression of the Dorsal Root Ganglion Pain

The present protocol describes a practical strategy to expedite the verification step of stereotaxic injection coordinates before conducting viral tracing using dyes and frozen sections.

Preliminary Validation of Stereotaxic Injection Coordinates via Cryosectioning

Dorsal root ganglia (DRG) contain primary sensory neuron cell bodies and relay peripheral sensory signals to the spinal cord. This protocol describes a method for mouse DRG dissection that supports standardized isolation of structurally intact ganglia, anatomical segmental identification, intuitive guidance for novice users, and reduced procedural tissue injury.

Dissection and Isolation of Mouse Dorsal Root Ganglia

Learn a reliable cryostat sectioning method for mouse dorsal root ganglion tissue to obtain high-quality, flat cross-sections. This protocol enables precise immunohistochemistry studies in neuroscience research.

A Procedure for Mouse Dorsal Root Ganglion Cryosectioning

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