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An in vitro assay to study induction of the regenerative state in sensory neurons
After injury, peripheral neurons activate a pro-regenerative program that facilitates axon regeneration. While many regeneration-associated genes have been identified, the mechanism by which injury activates this program is less well understood. Furthermore, identifying pharmacological methods to in...
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Published in: | Experimental neurology 2015-01, Vol.263, p.350-363 |
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creator | Frey, E. Valakh, V. Karney-Grobe, S. Shi, Y. Milbrandt, J. DiAntonio, A. |
description | After injury, peripheral neurons activate a pro-regenerative program that facilitates axon regeneration. While many regeneration-associated genes have been identified, the mechanism by which injury activates this program is less well understood. Furthermore, identifying pharmacological methods to induce a pro-regenerative state could lead to novel treatments to repair the injured nervous system. Therefore, we have developed an in vitro assay to study induction of the pro-regenerative state following injury or pharmacological treatment. First, we took advantage of the observation that dissociating and culturing sensory neurons from dorsal root ganglia activates a pro-regenerative program. We show that cultured neurons activate transcription factors and upregulate regeneration-associated genes common to the pro-regenerative program within the first hours after dissection. In a paradigm similar to pre-conditioning, neurons injured by dissociation display enhanced neurite outgrowth when replated as early as 12h after being removed from the animal. Furthermore, stimulation of the pro-regenerative state improves growth on inhibitory substrates and requires DLK/JNK signaling, both hallmarks of the pro-regeneration response in vivo. Finally, we modified this assay in order to identify new methods to activate the pro-regenerative state in an effort to mimic the pre-conditioning effect. We report that after several days in culture, neurons down-regulate many molecular hallmarks of injury and no longer display enhanced neurite outgrowth after replating. Hence, these neurons are functionally naïve and are a useful tool for identifying methods to induce the pro-regenerative state. We show that both injury and pre-treatment with forskolin reactivate the pro-regenerative state in this paradigm. Hence, this assay is useful for identifying pharmacological agents that induce the pro-regenerative state in the absence of injury.
•Dissection and dissociation of DRG neurons activates a pro-regenerative response.•The regenerative response fades in culture resulting in functionally naïve neurons.•Injury or Forskolin re-induce the regenerative response of functionally naïve neurons.•Assay can identify drugs that induce regenerative response in the absence of injury. |
doi_str_mv | 10.1016/j.expneurol.2014.10.012 |
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•Dissection and dissociation of DRG neurons activates a pro-regenerative response.•The regenerative response fades in culture resulting in functionally naïve neurons.•Injury or Forskolin re-induce the regenerative response of functionally naïve neurons.•Assay can identify drugs that induce regenerative response in the absence of injury.</description><identifier>ISSN: 0014-4886</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1016/j.expneurol.2014.10.012</identifier><identifier>PMID: 25447942</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Axon regeneration ; Cells, Cultured ; cJun N-terminal kinase (JNK) ; Dorsal root ganglion (DRG) ; Dual leucine zipper kinase (DLK) ; Ganglia, Spinal - physiology ; Immunohistochemistry ; In Vitro Techniques ; Mice ; Mice, Inbred C57BL ; Nerve Regeneration - physiology ; Real-Time Polymerase Chain Reaction ; Replating assay ; Sensory Receptor Cells - physiology ; Superior cervical ganglion 10 (SCG10)</subject><ispartof>Experimental neurology, 2015-01, Vol.263, p.350-363</ispartof><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><rights>2014 Elsevier Inc. All rights reserved. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-5134f6d9deed297713af35a22a628a6a7ddd559cc72b5a3056ecde46835a29fc3</citedby><cites>FETCH-LOGICAL-c508t-5134f6d9deed297713af35a22a628a6a7ddd559cc72b5a3056ecde46835a29fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25447942$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frey, E.</creatorcontrib><creatorcontrib>Valakh, V.</creatorcontrib><creatorcontrib>Karney-Grobe, S.</creatorcontrib><creatorcontrib>Shi, Y.</creatorcontrib><creatorcontrib>Milbrandt, J.</creatorcontrib><creatorcontrib>DiAntonio, A.</creatorcontrib><title>An in vitro assay to study induction of the regenerative state in sensory neurons</title><title>Experimental neurology</title><addtitle>Exp Neurol</addtitle><description>After injury, peripheral neurons activate a pro-regenerative program that facilitates axon regeneration. While many regeneration-associated genes have been identified, the mechanism by which injury activates this program is less well understood. Furthermore, identifying pharmacological methods to induce a pro-regenerative state could lead to novel treatments to repair the injured nervous system. Therefore, we have developed an in vitro assay to study induction of the pro-regenerative state following injury or pharmacological treatment. First, we took advantage of the observation that dissociating and culturing sensory neurons from dorsal root ganglia activates a pro-regenerative program. We show that cultured neurons activate transcription factors and upregulate regeneration-associated genes common to the pro-regenerative program within the first hours after dissection. In a paradigm similar to pre-conditioning, neurons injured by dissociation display enhanced neurite outgrowth when replated as early as 12h after being removed from the animal. Furthermore, stimulation of the pro-regenerative state improves growth on inhibitory substrates and requires DLK/JNK signaling, both hallmarks of the pro-regeneration response in vivo. Finally, we modified this assay in order to identify new methods to activate the pro-regenerative state in an effort to mimic the pre-conditioning effect. We report that after several days in culture, neurons down-regulate many molecular hallmarks of injury and no longer display enhanced neurite outgrowth after replating. Hence, these neurons are functionally naïve and are a useful tool for identifying methods to induce the pro-regenerative state. We show that both injury and pre-treatment with forskolin reactivate the pro-regenerative state in this paradigm. Hence, this assay is useful for identifying pharmacological agents that induce the pro-regenerative state in the absence of injury.
•Dissection and dissociation of DRG neurons activates a pro-regenerative response.•The regenerative response fades in culture resulting in functionally naïve neurons.•Injury or Forskolin re-induce the regenerative response of functionally naïve neurons.•Assay can identify drugs that induce regenerative response in the absence of injury.</description><subject>Animals</subject><subject>Axon regeneration</subject><subject>Cells, Cultured</subject><subject>cJun N-terminal kinase (JNK)</subject><subject>Dorsal root ganglion (DRG)</subject><subject>Dual leucine zipper kinase (DLK)</subject><subject>Ganglia, Spinal - physiology</subject><subject>Immunohistochemistry</subject><subject>In Vitro Techniques</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Nerve Regeneration - physiology</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Replating assay</subject><subject>Sensory Receptor Cells - physiology</subject><subject>Superior cervical ganglion 10 (SCG10)</subject><issn>0014-4886</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkU1vEzEQhi0EomnhL8AeuWwYf-7uBSmq-KhUCSHB2XLt2dbRxg62NyL_Hi8pEZzgZGve550Z-yXkNYU1Barebtf4Yx9wTnFaM6CiVtdA2ROyojBAywSHp2QFVWlF36sLcpnzFgAGwbrn5IJJIbp6X5Evm9D40Bx8SbExOZtjU2KTy-yOte5mW3wMTRyb8oBNwnsMmEzxB6yMKbh4M4Yc07H5tU7IL8iz0UwZXz6eV-Tbh_dfrz-1t58_3lxvblsroS-tpFyMyg0O0bGh6yg3I5eGMaNYb5TpnHNSDtZ27E4aDlKhdShUv0DDaPkVeXfqu5_vdugshpLMpPfJ70w66mi8_lsJ_kHfx4MWTCmhRG3w5rFBit9nzEXvfLY4TSZgnLOmSgEfGGXyP1AuATgwqGh3Qm2KOScczxtR0Et2eqvP2eklu0Wo2VXnqz8fdPb9DqsCmxOA9VsPHpPO1mOw6HxCW7SL_p9DfgJpB7E3</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Frey, E.</creator><creator>Valakh, V.</creator><creator>Karney-Grobe, S.</creator><creator>Shi, Y.</creator><creator>Milbrandt, J.</creator><creator>DiAntonio, A.</creator><general>Elsevier Inc</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><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20150101</creationdate><title>An in vitro assay to study induction of the regenerative state in sensory neurons</title><author>Frey, E. ; Valakh, V. ; Karney-Grobe, S. ; Shi, Y. ; Milbrandt, J. ; DiAntonio, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-5134f6d9deed297713af35a22a628a6a7ddd559cc72b5a3056ecde46835a29fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Axon regeneration</topic><topic>Cells, Cultured</topic><topic>cJun N-terminal kinase (JNK)</topic><topic>Dorsal root ganglion (DRG)</topic><topic>Dual leucine zipper kinase (DLK)</topic><topic>Ganglia, Spinal - physiology</topic><topic>Immunohistochemistry</topic><topic>In Vitro Techniques</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Nerve Regeneration - physiology</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Replating assay</topic><topic>Sensory Receptor Cells - physiology</topic><topic>Superior cervical ganglion 10 (SCG10)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frey, E.</creatorcontrib><creatorcontrib>Valakh, V.</creatorcontrib><creatorcontrib>Karney-Grobe, S.</creatorcontrib><creatorcontrib>Shi, Y.</creatorcontrib><creatorcontrib>Milbrandt, J.</creatorcontrib><creatorcontrib>DiAntonio, A.</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><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frey, E.</au><au>Valakh, V.</au><au>Karney-Grobe, S.</au><au>Shi, Y.</au><au>Milbrandt, J.</au><au>DiAntonio, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An in vitro assay to study induction of the regenerative state in sensory neurons</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>263</volume><spage>350</spage><epage>363</epage><pages>350-363</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><abstract>After injury, peripheral neurons activate a pro-regenerative program that facilitates axon regeneration. While many regeneration-associated genes have been identified, the mechanism by which injury activates this program is less well understood. Furthermore, identifying pharmacological methods to induce a pro-regenerative state could lead to novel treatments to repair the injured nervous system. Therefore, we have developed an in vitro assay to study induction of the pro-regenerative state following injury or pharmacological treatment. First, we took advantage of the observation that dissociating and culturing sensory neurons from dorsal root ganglia activates a pro-regenerative program. We show that cultured neurons activate transcription factors and upregulate regeneration-associated genes common to the pro-regenerative program within the first hours after dissection. In a paradigm similar to pre-conditioning, neurons injured by dissociation display enhanced neurite outgrowth when replated as early as 12h after being removed from the animal. Furthermore, stimulation of the pro-regenerative state improves growth on inhibitory substrates and requires DLK/JNK signaling, both hallmarks of the pro-regeneration response in vivo. Finally, we modified this assay in order to identify new methods to activate the pro-regenerative state in an effort to mimic the pre-conditioning effect. We report that after several days in culture, neurons down-regulate many molecular hallmarks of injury and no longer display enhanced neurite outgrowth after replating. Hence, these neurons are functionally naïve and are a useful tool for identifying methods to induce the pro-regenerative state. We show that both injury and pre-treatment with forskolin reactivate the pro-regenerative state in this paradigm. Hence, this assay is useful for identifying pharmacological agents that induce the pro-regenerative state in the absence of injury.
•Dissection and dissociation of DRG neurons activates a pro-regenerative response.•The regenerative response fades in culture resulting in functionally naïve neurons.•Injury or Forskolin re-induce the regenerative response of functionally naïve neurons.•Assay can identify drugs that induce regenerative response in the absence of injury.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25447942</pmid><doi>10.1016/j.expneurol.2014.10.012</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Axon regeneration Cells, Cultured cJun N-terminal kinase (JNK) Dorsal root ganglion (DRG) Dual leucine zipper kinase (DLK) Ganglia, Spinal - physiology Immunohistochemistry In Vitro Techniques Mice Mice, Inbred C57BL Nerve Regeneration - physiology Real-Time Polymerase Chain Reaction Replating assay Sensory Receptor Cells - physiology Superior cervical ganglion 10 (SCG10) |
title | An in vitro assay to study induction of the regenerative state in sensory neurons |
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