An improved method for in vitro morphofunctional analysis of mouse dorsal root ganglia
Sensory neurons in dorsal root ganglia (DRGs) are the first-order neurons along the pathway conveying sensory information from the periphery to the central nervous system. The analysis of the morphological and physiological features of these neurons and their alterations in pathology is the necessar...
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Veröffentlicht in: | Annals of anatomy 2016-09, Vol.207, p.62-67 |
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description | Sensory neurons in dorsal root ganglia (DRGs) are the first-order neurons along the pathway conveying sensory information from the periphery to the central nervous system. The analysis of the morphological and physiological features of these neurons and their alterations in pathology is the necessary prerequisite to understand pain encoding mechanisms. Here, we describe an in vitro procedure for combined morphofunctional analysis of mouse DRGs. Freshly excised DRGs obtained from adult mice were incubated in collagenase to dissolve the ensheathing connective capsule. The degradation of the connective tissue facilitates both access to the neurons by classical recording glass pipettes and the penetration of primary antibodies for immunohistochemical procedures. The entire DRGs were then imaged using a confocal microscope obtaining a fine 3D representation of their cytoarchitecture without requiring tissue sectioning. Thus, our proposed whole-mount preparation represents a flexible in vitro approach for both functional and phenotypic analysis of DRG neurons by at the same time preserving their neuroanatomical relationships. |
doi_str_mv | 10.1016/j.aanat.2016.04.032 |
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The analysis of the morphological and physiological features of these neurons and their alterations in pathology is the necessary prerequisite to understand pain encoding mechanisms. Here, we describe an in vitro procedure for combined morphofunctional analysis of mouse DRGs. Freshly excised DRGs obtained from adult mice were incubated in collagenase to dissolve the ensheathing connective capsule. The degradation of the connective tissue facilitates both access to the neurons by classical recording glass pipettes and the penetration of primary antibodies for immunohistochemical procedures. The entire DRGs were then imaged using a confocal microscope obtaining a fine 3D representation of their cytoarchitecture without requiring tissue sectioning. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-7e6928c1e7ac6a88d3513eabd40a7a089b6132c34224a8adfbe98b11333264423</citedby><cites>FETCH-LOGICAL-c359t-7e6928c1e7ac6a88d3513eabd40a7a089b6132c34224a8adfbe98b11333264423</cites><orcidid>0000-0002-4956-3563</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0940960216300875$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27224901$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ciglieri, E.</creatorcontrib><creatorcontrib>Ferrini, F.</creatorcontrib><creatorcontrib>Boggio, E.</creatorcontrib><creatorcontrib>Salio, C.</creatorcontrib><title>An improved method for in vitro morphofunctional analysis of mouse dorsal root ganglia</title><title>Annals of anatomy</title><addtitle>Ann Anat</addtitle><description>Sensory neurons in dorsal root ganglia (DRGs) are the first-order neurons along the pathway conveying sensory information from the periphery to the central nervous system. The analysis of the morphological and physiological features of these neurons and their alterations in pathology is the necessary prerequisite to understand pain encoding mechanisms. Here, we describe an in vitro procedure for combined morphofunctional analysis of mouse DRGs. Freshly excised DRGs obtained from adult mice were incubated in collagenase to dissolve the ensheathing connective capsule. The degradation of the connective tissue facilitates both access to the neurons by classical recording glass pipettes and the penetration of primary antibodies for immunohistochemical procedures. The entire DRGs were then imaged using a confocal microscope obtaining a fine 3D representation of their cytoarchitecture without requiring tissue sectioning. Thus, our proposed whole-mount preparation represents a flexible in vitro approach for both functional and phenotypic analysis of DRG neurons by at the same time preserving their neuroanatomical relationships.</description><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Collagenases - chemistry</subject><subject>DRG</subject><subject>Ganglia, Spinal - cytology</subject><subject>Ganglia, Spinal - physiology</subject><subject>Image Enhancement - methods</subject><subject>Immunohistochemistry</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Mice</subject><subject>Microscopy, Confocal - methods</subject><subject>Nociceptors</subject><subject>Patch clamp</subject><subject>Patch-Clamp Techniques - methods</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Sensory Receptor Cells - chemistry</subject><subject>Sensory Receptor Cells - cytology</subject><subject>Sensory Receptor Cells - physiology</subject><subject>Structure-Activity Relationship</subject><subject>Whole-mount</subject><issn>0940-9602</issn><issn>1618-0402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwBUjISzYJftVNFiyqipdUiQ2wtRx70rpK4mInlfr3uBRYshqN5t65Mweha0pySqi82-Rad7rPWWpyInLC2QkaU0mLjAjCTtGYlIJkpSRshC5i3BDC5VSKczRiM8ZESegYfcw77Npt8DuwuIV-7S2ufcCuwzvXB49bH7ZrXw-d6Z3vdINTZrOPLmJfp-EQAVsfYhoE73u80t2qcfoSndW6iXD1Uyfo_fHhbfGcLV-fXhbzZWb4tOyzGciSFYbCTBupi8LyKeWgKyuInmlSlJWknBku0rm60LauoCwqSjnnTArB-ATdHvemDz4HiL1qXTTQNLqDdJuiBRVSJsM0SflRaoKPMUCttsG1OuwVJeoAVG3UN1B1AKqIUAloct38BAxVC_bP80swCe6PAkhv7hwEFY2DzoB1AUyvrHf_BnwBIKGH8g</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Ciglieri, E.</creator><creator>Ferrini, F.</creator><creator>Boggio, E.</creator><creator>Salio, C.</creator><general>Elsevier GmbH</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4956-3563</orcidid></search><sort><creationdate>20160901</creationdate><title>An improved method for in vitro morphofunctional analysis of mouse dorsal root ganglia</title><author>Ciglieri, E. ; Ferrini, F. ; Boggio, E. ; Salio, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-7e6928c1e7ac6a88d3513eabd40a7a089b6132c34224a8adfbe98b11333264423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Collagenases - chemistry</topic><topic>DRG</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Spinal - physiology</topic><topic>Image Enhancement - methods</topic><topic>Immunohistochemistry</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Mice</topic><topic>Microscopy, Confocal - methods</topic><topic>Nociceptors</topic><topic>Patch clamp</topic><topic>Patch-Clamp Techniques - methods</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Sensory Receptor Cells - chemistry</topic><topic>Sensory Receptor Cells - cytology</topic><topic>Sensory Receptor Cells - physiology</topic><topic>Structure-Activity Relationship</topic><topic>Whole-mount</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ciglieri, E.</creatorcontrib><creatorcontrib>Ferrini, F.</creatorcontrib><creatorcontrib>Boggio, E.</creatorcontrib><creatorcontrib>Salio, C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of anatomy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ciglieri, E.</au><au>Ferrini, F.</au><au>Boggio, E.</au><au>Salio, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An improved method for in vitro morphofunctional analysis of mouse dorsal root ganglia</atitle><jtitle>Annals of anatomy</jtitle><addtitle>Ann Anat</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>207</volume><spage>62</spage><epage>67</epage><pages>62-67</pages><issn>0940-9602</issn><eissn>1618-0402</eissn><abstract>Sensory neurons in dorsal root ganglia (DRGs) are the first-order neurons along the pathway conveying sensory information from the periphery to the central nervous system. 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subjects | Animals Cells, Cultured Collagenases - chemistry DRG Ganglia, Spinal - cytology Ganglia, Spinal - physiology Image Enhancement - methods Immunohistochemistry In Vitro Techniques Male Mice Microscopy, Confocal - methods Nociceptors Patch clamp Patch-Clamp Techniques - methods Reproducibility of Results Sensitivity and Specificity Sensory Receptor Cells - chemistry Sensory Receptor Cells - cytology Sensory Receptor Cells - physiology Structure-Activity Relationship Whole-mount |
title | An improved method for in vitro morphofunctional analysis of mouse dorsal root ganglia |
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