<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Umbaugh DS</submitter><funding>Midwest Stem Cell Center</funding><funding>National Institute of General Medicine Liver Disease COBRE</funding><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIGMS NIH HHS</funding><funding>Midwest Biomedical Accelerator Consortium, an NIH Research Evaluation and Commercialization Hub</funding><pagination>3315-3329</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9773902</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>96(12)</volume><pubmed_abstract>The persistence of hepatotoxicity induced by N-acetyl-para-aminophenol (Acetaminophen or Paracetamol, abbreviated as APAP) as the most common cause of acute liver failure in the United States, despite the availability of N-acetylcysteine, illustrates the clinical relevance of additional therapeutic approaches. While human mesenchymal stem cells (MSCs) have shown protection in mouse models of liver injury, the MSCs used are generally not cleared for human use and it is unclear whether these effects are due to xenotransplantation. Here we evaluated GMP manufactured clinical grade human Wharton's Jelly mesenchymal stem cells (WJMSCs), which are currently being investigated in human clinical trials, in a mouse model of APAP hepatotoxicity in comparison to human dermal fibroblasts (HDFs) to add</pubmed_abstract><journal>Archives of toxicology</journal><pubmed_title>Human Wharton's Jelly-derived mesenchymal stem cells prevent acetaminophen-induced liver injury in a mouse model unlike human dermal fibroblasts.</pubmed_title><pmcid>PMC9773902</pmcid><funding_grant_id>P20 GM103549</funding_grant_id><funding_grant_id>R01 DK102142</funding_grant_id><funding_grant_id>R01 DK098414</funding_grant_id><funding_grant_id>P30 GM118247</funding_grant_id><funding_grant_id>DK125465</funding_grant_id><funding_grant_id>R01 DK125465</funding_grant_id><pubmed_authors>Duan L</pubmed_authors><pubmed_authors>Woolbright B</pubmed_authors><pubmed_authors>Soder RP</pubmed_authors><pubmed_authors>Ramachandran A</pubmed_authors><pubmed_authors>Umbaugh DS</pubmed_authors><pubmed_authors>Nguyen NT</pubmed_authors><pubmed_authors>Robarts DR</pubmed_authors><pubmed_authors>Jaeschke H</pubmed_authors><pubmed_authors>Adelusi O</pubmed_authors><pubmed_authors>Abhyankar S</pubmed_authors><pubmed_authors>Dawn B</pubmed_authors><pubmed_authors>Apte U</pubmed_authors></additional><is_claimable>false</is_claimable><name>Human Wharton's Jelly-derived mesenchymal stem cells prevent acetaminophen-induced liver injury in a mouse model unlike human dermal fibroblasts.</name><description>The persistence of hepatotoxicity induced by N-acetyl-para-aminophenol (Acetaminophen or Paracetamol, abbreviated as APAP) as the most common cause of acute liver failure in the United States, despite the availability of N-acetylcysteine, illustrates the clinical relevance of additional therapeutic approaches. While human mesenchymal stem cells (MSCs) have shown protection in mouse models of liver injury, the MSCs used are generally not cleared for human use and it is unclear whether these effects are due to xenotransplantation. Here we evaluated GMP manufactured clinical grade human Wharton's Jelly mesenchymal stem cells (WJMSCs), which are currently being investigated in human clinical trials, in a mouse model of APAP hepatotoxicity in comparison to human dermal fibroblasts (HDFs) to add</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-05-29T21:47:02.503Z</modification><creation>2025-05-29T21:47:02.503Z</creation></dates><accession>S-EPMC9773902</accession><cross_references><pubmed>36057886</pubmed><doi>10.1007/s00204-022-03372-5</doi></cross_references></HashMap>