<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yamada D</submitter><funding>Japan Agency for Medical Research and Development</funding><pagination>2661</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8910499</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(5)</volume><pubmed_abstract>Stem cell-based therapies and experimental methods rely on efficient induction of human pluripotent stem cells (hPSCs). During limb development, the lateral plate mesoderm (LPM) produces limb-bud mesenchymal (LBM) cells that differentiate into osteochondroprogenitor cells and form cartilage tissues in the appendicular skeleton. Previously, we generated PRRX1-tdTomato reporter hPSCs to establish the protocol for inducing the hPSC-derived PRRX1+ LBM-like cells. However, surface antigens that assess the induction efficiency of hPSC-derived PRRX1+ LBM-like cells from LPM have not been identified. Here, we used PRRX1-tdTomato reporter hPSCs and found that high pluripotent cell density suppressed the expression of PRRX1 mRNA and tdTomato after LBM-like induction. RNA sequencing and flow cytometr</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Identification of Surface Antigens That Define Human Pluripotent Stem Cell-Derived PRRX1+Limb-Bud-like Mesenchymal Cells.</pubmed_title><pmcid>PMC8910499</pmcid><funding_grant_id>18bm0704024h0001</funding_grant_id><funding_grant_id>20bm0404064h0001</funding_grant_id><pubmed_authors>Nakata E</pubmed_authors><pubmed_authors>Takao T</pubmed_authors><pubmed_authors>Nakamura M</pubmed_authors><pubmed_authors>Kitano T</pubmed_authors><pubmed_authors>Yamada D</pubmed_authors><pubmed_authors>Takarada T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of Surface Antigens That Define Human Pluripotent Stem Cell-Derived PRRX1+Limb-Bud-like Mesenchymal Cells.</name><description>Stem cell-based therapies and experimental methods rely on efficient induction of human pluripotent stem cells (hPSCs). During limb development, the lateral plate mesoderm (LPM) produces limb-bud mesenchymal (LBM) cells that differentiate into osteochondroprogenitor cells and form cartilage tissues in the appendicular skeleton. Previously, we generated PRRX1-tdTomato reporter hPSCs to establish the protocol for inducing the hPSC-derived PRRX1+ LBM-like cells. However, surface antigens that assess the induction efficiency of hPSC-derived PRRX1+ LBM-like cells from LPM have not been identified. Here, we used PRRX1-tdTomato reporter hPSCs and found that high pluripotent cell density suppressed the expression of PRRX1 mRNA and tdTomato after LBM-like induction. RNA sequencing and flow cytometr</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-18T12:09:35.594Z</modification><creation>2025-04-06T21:49:36.588Z</creation></dates><accession>S-EPMC8910499</accession><cross_references><pubmed>35269809</pubmed><doi>10.3390/ijms23052661</doi></cross_references></HashMap>