<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chalasani SH</submitter><funding>NINDS NIH HHS</funding><pagination>4601-12</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6740796</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(11)</volume><pubmed_abstract>The chemokine receptor CXCR4 is expressed in the embryonic and mature CNS, yet its normal physiological function in neurons remains obscure. Here, we show that its cognate chemokine, stromal cell-derived factor-1 (SDF-1), promotes the survival of cultured embryonic retinal ganglion cell neurons even in the absence of other neurotrophic factors. This survival effect is mediated primarily through a cAMP-dependent pathway that acts through protein kinase A and MAP kinase. Addition of SDF-1 to a human neuronal cell line induces phosphorylation of p44/p42 MAP kinase and GSK3beta. Mouse embryos lacking the CXCR4 receptor have a reduced number of retinal ganglion cells. The ligand of CXCR4, SDF-1, may therefore provide generalized trophic support to neurons during their development and maturation</pubmed_abstract><journal>The Journal of neuroscience : the official journal of the Society for Neuroscience</journal><pubmed_title>The chemokine stromal cell-derived factor-1 promotes the survival of embryonic retinal ganglion cells.</pubmed_title><pmcid>PMC6740796</pmcid><funding_grant_id>R01 NS026527</funding_grant_id><funding_grant_id>R01-NS26527</funding_grant_id><pubmed_authors>Baribaud F</pubmed_authors><pubmed_authors>Doms RW</pubmed_authors><pubmed_authors>Littman DR</pubmed_authors><pubmed_authors>Coughlan CM</pubmed_authors><pubmed_authors>Lee VM</pubmed_authors><pubmed_authors>Raper JA</pubmed_authors><pubmed_authors>Chalasani SH</pubmed_authors><pubmed_authors>Sunshine MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>The chemokine stromal cell-derived factor-1 promotes the survival of embryonic retinal ganglion cells.</name><description>The chemokine receptor CXCR4 is expressed in the embryonic and mature CNS, yet its normal physiological function in neurons remains obscure. Here, we show that its cognate chemokine, stromal cell-derived factor-1 (SDF-1), promotes the survival of cultured embryonic retinal ganglion cell neurons even in the absence of other neurotrophic factors. This survival effect is mediated primarily through a cAMP-dependent pathway that acts through protein kinase A and MAP kinase. Addition of SDF-1 to a human neuronal cell line induces phosphorylation of p44/p42 MAP kinase and GSK3beta. Mouse embryos lacking the CXCR4 receptor have a reduced number of retinal ganglion cells. The ligand of CXCR4, SDF-1, may therefore provide generalized trophic support to neurons during their development and maturation</description><dates><release>2003-01-01T00:00:00Z</release><publication>2003 Jun</publication><modification>2025-04-04T12:25:43.764Z</modification><creation>2019-09-26T07:05:50Z</creation></dates><accession>S-EPMC6740796</accession><cross_references><pubmed>12805300</pubmed><doi>10.1523/jneurosci.23-11-04601.2003</doi><doi>10.1523/JNEUROSCI.23-11-04601.2003</doi></cross_references></HashMap>