<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bertaux-Skeirik N</submitter><funding>BLRD VA</funding><funding>University of Cincinnati Graduate School Dean&amp;apos;s Fellowship</funding><funding>National Institutes of Health</funding><funding>Albert J Ryan Fellowship</funding><funding>National Institute of General Medical Sciences</funding><funding>College of Medicine Bridge Funding Program</funding><funding>Department of Veterans Affairs Merit Review Award</funding><funding>NIDDK NIH HHS</funding><funding>Presbyterian Historical Society</funding><funding>NCI NIH HHS</funding><funding>NIAMS NIH HHS</funding><funding>National Cancer Institute of the National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><pagination>463-475</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5591948</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>242(4)</volume><pubmed_abstract>The CD44 gene encodes several protein isoforms due to alternative splicing and post translational modifications. Given that CD44 variant isoform 9 (CD44v9) is expressed within Spasmolytic Polypeptide/TFF2-Expressing Metaplasia (SPEM) glands during repair, CD44v9 may be play a funcitonal role during the process of regeneration of the gastric epithelium. Here we hypothesize that CD44v9 marks a regenerative cell lineage responsive to infiltrating macrophages during regeneration of the gastric epithelium. Ulcers were induced in CD44-deficient (CD44KO) and C57BL/6 (BL6) mice by a localized application of acetic acid to the serosal surface of the stomach. Gastric organoids expressing CD44v9 were derived from mouse stomachs and transplanted at the ulcer site of CD44KO mice. Ulcers, CD44v9 express</pubmed_abstract><journal>The Journal of pathology</journal><pubmed_title>CD44 variant isoform 9 emerges in response to injury and contributes to the regeneration of the gastric epithelium.</pubmed_title><pmcid>PMC5591948</pmcid><funding_grant_id>R01 DK083402</funding_grant_id><funding_grant_id>R50 CA211404</funding_grant_id><funding_grant_id>P30 DK078392</funding_grant_id><funding_grant_id>P30 DK058404</funding_grant_id><funding_grant_id>I01 BX000930</funding_grant_id><funding_grant_id>I01BX000930</funding_grant_id><funding_grant_id>P30 AR047363</funding_grant_id><funding_grant_id>R01 DK071590</funding_grant_id><funding_grant_id>2 R01 DK083402-06</funding_grant_id><funding_grant_id>T32 GM105526</funding_grant_id><funding_grant_id>R50CA211404</funding_grant_id><funding_grant_id>AR-47363</funding_grant_id><funding_grant_id>T32 CA106183</funding_grant_id><funding_grant_id>2T32GM105526-04</funding_grant_id><pubmed_authors>Biesiada J</pubmed_authors><pubmed_authors>Sundaram N</pubmed_authors><pubmed_authors>Hawkins J</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Engevik AC</pubmed_authors><pubmed_authors>Jian G</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Mahe M</pubmed_authors><pubmed_authors>Medvedovic M</pubmed_authors><pubmed_authors>Chakrabarti J</pubmed_authors><pubmed_authors>Teal E</pubmed_authors><pubmed_authors>Goldenring JR</pubmed_authors><pubmed_authors>Mulloy JC</pubmed_authors><pubmed_authors>Qualls JE</pubmed_authors><pubmed_authors>Helmrath MA</pubmed_authors><pubmed_authors>Diwan T</pubmed_authors><pubmed_authors>Zavros Y</pubmed_authors><pubmed_authors>Wunderlich M</pubmed_authors><pubmed_authors>Bertaux-Skeirik N</pubmed_authors><pubmed_authors>Gabre J</pubmed_authors></additional><is_claimable>false</is_claimable><name>CD44 variant isoform 9 emerges in response to injury and contributes to the regeneration of the gastric epithelium.</name><description>The CD44 gene encodes several protein isoforms due to alternative splicing and post translational modifications. Given that CD44 variant isoform 9 (CD44v9) is expressed within Spasmolytic Polypeptide/TFF2-Expressing Metaplasia (SPEM) glands during repair, CD44v9 may be play a funcitonal role during the process of regeneration of the gastric epithelium. Here we hypothesize that CD44v9 marks a regenerative cell lineage responsive to infiltrating macrophages during regeneration of the gastric epithelium. Ulcers were induced in CD44-deficient (CD44KO) and C57BL/6 (BL6) mice by a localized application of acetic acid to the serosal surface of the stomach. Gastric organoids expressing CD44v9 were derived from mouse stomachs and transplanted at the ulcer site of CD44KO mice. Ulcers, CD44v9 express</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Aug</publication><modification>2025-04-19T08:43:14.851Z</modification><creation>2019-03-27T02:55:58Z</creation></dates><accession>S-EPMC5591948</accession><cross_references><pubmed>28497484</pubmed><doi>10.1002/path.4918</doi></cross_references></HashMap>