<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chiu H</submitter><funding>NIGMS NIH HHS</funding><pagination>4842</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6242819</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>Two important biological events happen coincidently soon after nerve injury in the peripheral nervous system in C. elegans: removal of axon debris and initiation of axon regeneration. But, it is not known how these two events are co-regulated. Mutants of ced-1, a homolog of Draper and MEGF10, display defects in both events. One model is that those events could be related. But our data suggest that they are actually separable. CED-1 functions in the muscle-type engulfing cells in both events and is enriched in muscle protrusions in close contact with axon debris and regenerating axons. Its two functions occur through distinct biochemical mechanisms; extracellular domain-mediated adhesion for regeneration and extracellular domain binding-induced intracellular domain signaling for debris remo</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Engulfing cells promote neuronal regeneration and remove neuronal debris through distinct biochemical functions of CED-1.</pubmed_title><pmcid>PMC6242819</pmcid><funding_grant_id>R01 GM098026</funding_grant_id><funding_grant_id>R01 GM111320</funding_grant_id><pubmed_authors>Hsieh YW</pubmed_authors><pubmed_authors>Zou Y</pubmed_authors><pubmed_authors>Wu YC</pubmed_authors><pubmed_authors>Suzuki N</pubmed_authors><pubmed_authors>Chiu H</pubmed_authors><pubmed_authors>Chuang CF</pubmed_authors><pubmed_authors>Chang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Engulfing cells promote neuronal regeneration and remove neuronal debris through distinct biochemical functions of CED-1.</name><description>Two important biological events happen coincidently soon after nerve injury in the peripheral nervous system in C. elegans: removal of axon debris and initiation of axon regeneration. But, it is not known how these two events are co-regulated. Mutants of ced-1, a homolog of Draper and MEGF10, display defects in both events. One model is that those events could be related. But our data suggest that they are actually separable. CED-1 functions in the muscle-type engulfing cells in both events and is enriched in muscle protrusions in close contact with axon debris and regenerating axons. Its two functions occur through distinct biochemical mechanisms; extracellular domain-mediated adhesion for regeneration and extracellular domain binding-induced intracellular domain signaling for debris remo</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2025-04-04T08:41:18.228Z</modification><creation>2019-03-27T00:08:32Z</creation></dates><accession>S-EPMC6242819</accession><cross_references><pubmed>30451835</pubmed><doi>10.1038/s41467-018-07291-x</doi></cross_references></HashMap>