<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Villa-Hernandez S</submitter><funding>Wellcome Trust</funding><pagination>15-29</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7618384</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>129</volume><pubmed_abstract>Neuropathic pain is a particularly intractable type of chronic pain that can result from physical nerve damage due to surgery or entrapment. Here, we present data which suggest that a particular subclass of fibroblast and mural cells may be implicated in the sensory neuron dysfunction that is characteristic of this pain state. In a mouse model of traumatic painful neuropathy, we used cell sorting, nerve tissue clearing and RNA sequencing to study stromal cells. With cell sorting (n = 4 mouse nerves) and tissue clearing (n = 5), we show that fibroblasts and mural cells positive for the platelet-derived growth factor receptor beta (Pdgfrb) gene are increased in number for at least two months post-nerve damage. Moreover, single cell RNA sequencing data (n = 4) from our own lab and those of th</pubmed_abstract><journal>Brain, behavior, and immunity</journal><pubmed_title>A role for fibroblast and mural cell subsets in a nerve ligation model of neuropathic pain?</pubmed_title><pmcid>PMC7618384</pmcid><funding_grant_id>224257/Z/21/Z</funding_grant_id><funding_grant_id>218452/Z/19/Z</funding_grant_id><funding_grant_id>224257</funding_grant_id><funding_grant_id>WT098051</funding_grant_id><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Davis H</pubmed_authors><pubmed_authors>Taams LS</pubmed_authors><pubmed_authors>Villa-Hernandez S</pubmed_authors><pubmed_authors>Walker JV</pubmed_authors><pubmed_authors>Zebochin I</pubmed_authors><pubmed_authors>Shimizu F</pubmed_authors><pubmed_authors>Denk F</pubmed_authors><pubmed_authors>Hore Z</pubmed_authors><pubmed_authors>Fedele L</pubmed_authors><pubmed_authors>Kanda T</pubmed_authors></additional><is_claimable>false</is_claimable><name>A role for fibroblast and mural cell subsets in a nerve ligation model of neuropathic pain?</name><description>Neuropathic pain is a particularly intractable type of chronic pain that can result from physical nerve damage due to surgery or entrapment. Here, we present data which suggest that a particular subclass of fibroblast and mural cells may be implicated in the sensory neuron dysfunction that is characteristic of this pain state. In a mouse model of traumatic painful neuropathy, we used cell sorting, nerve tissue clearing and RNA sequencing to study stromal cells. With cell sorting (n = 4 mouse nerves) and tissue clearing (n = 5), we show that fibroblasts and mural cells positive for the platelet-derived growth factor receptor beta (Pdgfrb) gene are increased in number for at least two months post-nerve damage. Moreover, single cell RNA sequencing data (n = 4) from our own lab and those of th</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-06T03:19:15.247Z</modification><creation>2026-06-06T03:07:08.905Z</creation></dates><accession>S-EPMC7618384</accession><cross_references><pubmed>40381746</pubmed><doi>10.1016/j.bbi.2025.05.012</doi></cross_references></HashMap>