<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ha SE</submitter><funding>NIDDK NIH HHS</funding><funding>NIH HHS</funding><pagination>5007</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9103908</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(9)</volume><pubmed_abstract>Metalloendopeptidase ADAM-Like Decysin 1 (ADAMDEC1) is an anti-inflammatory peptidase that is almost exclusively expressed in the gastrointestinal (GI) tract. We have recently found abundant and selective expression of Adamdec1 in colonic mucosal PDGFRα&lt;sup>+&lt;/sup> cells. However, the cellular origin for this gene expression is controversial as it is also known to be expressed in intestinal macrophages. We found that Adamdec1 mRNAs were selectively expressed in colonic mucosal subepithelial PDGFRα&lt;sup>+&lt;/sup> cells. ADAMDEC1 protein was mainly released from PDGFRα&lt;sup>+&lt;/sup> cells and accumulated in the mucosal layer lamina propria space near the epithelial basement membrane. PDGFRα&lt;sup>+&lt;/sup> cells significantly overexpressed Adamdec1 mRNAs and protein in DSS-induced colitis mice. Adamd</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Metalloendopeptidase ADAM-like Decysin 1 (ADAMDEC1) in Colonic Subepithelial PDGFRα&lt;sup>+&lt;/sup> Cells Is a New Marker for Inflammatory Bowel Disease.</pubmed_title><pmcid>PMC9103908</pmcid><funding_grant_id>P01 DK041315</funding_grant_id><funding_grant_id>R01 DK103055</funding_grant_id><funding_grant_id>R01DK094886</funding_grant_id><funding_grant_id>R01 DK094886</funding_grant_id><funding_grant_id>P01-DK41315</funding_grant_id><funding_grant_id>R01 DK091336</funding_grant_id><funding_grant_id>R01DK103055</funding_grant_id><pubmed_authors>Kim MS</pubmed_authors><pubmed_authors>Rubin SJS</pubmed_authors><pubmed_authors>Becker L</pubmed_authors><pubmed_authors>Sanders KM</pubmed_authors><pubmed_authors>Habtezion A</pubmed_authors><pubmed_authors>Baek G</pubmed_authors><pubmed_authors>Poudrier SM</pubmed_authors><pubmed_authors>Lee MY</pubmed_authors><pubmed_authors>Gottfried-Blackmore A</pubmed_authors><pubmed_authors>Jorgensen BG</pubmed_authors><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Choi SC</pubmed_authors><pubmed_authors>Jin B</pubmed_authors><pubmed_authors>Ro S</pubmed_authors><pubmed_authors>Ha SE</pubmed_authors><pubmed_authors>Singh R</pubmed_authors><pubmed_authors>Bartlett A</pubmed_authors><pubmed_authors>Zogg H</pubmed_authors><pubmed_authors>Wei L</pubmed_authors><pubmed_authors>Kim YS</pubmed_authors><pubmed_authors>Kurahashi M</pubmed_authors><pubmed_authors>Sasse KC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metalloendopeptidase ADAM-like Decysin 1 (ADAMDEC1) in Colonic Subepithelial PDGFRα&lt;sup>+&lt;/sup> Cells Is a New Marker for Inflammatory Bowel Disease.</name><description>Metalloendopeptidase ADAM-Like Decysin 1 (ADAMDEC1) is an anti-inflammatory peptidase that is almost exclusively expressed in the gastrointestinal (GI) tract. We have recently found abundant and selective expression of Adamdec1 in colonic mucosal PDGFRα&lt;sup>+&lt;/sup> cells. However, the cellular origin for this gene expression is controversial as it is also known to be expressed in intestinal macrophages. We found that Adamdec1 mRNAs were selectively expressed in colonic mucosal subepithelial PDGFRα&lt;sup>+&lt;/sup> cells. ADAMDEC1 protein was mainly released from PDGFRα&lt;sup>+&lt;/sup> cells and accumulated in the mucosal layer lamina propria space near the epithelial basement membrane. PDGFRα&lt;sup>+&lt;/sup> cells significantly overexpressed Adamdec1 mRNAs and protein in DSS-induced colitis mice. Adamd</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-04T22:53:42.189Z</modification><creation>2025-02-19T00:55:57.3Z</creation></dates><accession>S-EPMC9103908</accession><cross_references><pubmed>35563399</pubmed><doi>10.3390/ijms23095007</doi></cross_references></HashMap>