<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhu D</submitter><funding>NICHD NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NLM NIH HHS</funding><pagination>107494</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11301355</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>300(8)</volume><pubmed_abstract>The commitment of stem cells to differentiate into osteoblasts is a highly regulated and complex process that involves the coordination of extrinsic signals and intrinsic transcriptional machinery. While rodent osteoblastic differentiation has been extensively studied, research on human osteogenesis has been limited by cell sources and existing models. Here, we systematically dissect human pluripotent stem cell-derived osteoblasts to identify functional membrane proteins and their downstream transcriptional networks involved in human osteogenesis. Our results reveal an enrichment of type II transmembrane serine protease CORIN in humans but not rodent osteoblasts. Functional analyses demonstrated that CORIN depletion significantly impairs osteogenesis. Genome-wide chromatin immunoprecipitat</pubmed_abstract><journal>The Journal of biological chemistry</journal><pubmed_title>Systematic transcriptome profiling of hPSC-derived osteoblasts unveils CORIN's mastery in governing osteogenesis through CEBPD modulation.</pubmed_title><pmcid>PMC11301355</pmcid><funding_grant_id>R01 CA246130</funding_grant_id><funding_grant_id>R01 HL142704</funding_grant_id><funding_grant_id>K08 HD042136</funding_grant_id><funding_grant_id>R01 LM012806</funding_grant_id><pubmed_authors>Huang YW</pubmed_authors><pubmed_authors>Pang LK</pubmed_authors><pubmed_authors>Shen J</pubmed_authors><pubmed_authors>Bazer DA</pubmed_authors><pubmed_authors>Tu J</pubmed_authors><pubmed_authors>Kameoka J</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Zhao Z</pubmed_authors><pubmed_authors>Zhu D</pubmed_authors><pubmed_authors>Dai Y</pubmed_authors><pubmed_authors>Ambrose CG</pubmed_authors><pubmed_authors>Lu L</pubmed_authors><pubmed_authors>Huo Z</pubmed_authors><pubmed_authors>Phan TTT</pubmed_authors><pubmed_authors>Shoemaker R</pubmed_authors><pubmed_authors>Zhao R</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Xu A</pubmed_authors><pubmed_authors>Gingold JA</pubmed_authors><pubmed_authors>Gao X</pubmed_authors><pubmed_authors>Lee DF</pubmed_authors><pubmed_authors>Wang LL</pubmed_authors><pubmed_authors>Huang MF</pubmed_authors><pubmed_authors>Chi TY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Systematic transcriptome profiling of hPSC-derived osteoblasts unveils CORIN's mastery in governing osteogenesis through CEBPD modulation.</name><description>The commitment of stem cells to differentiate into osteoblasts is a highly regulated and complex process that involves the coordination of extrinsic signals and intrinsic transcriptional machinery. While rodent osteoblastic differentiation has been extensively studied, research on human osteogenesis has been limited by cell sources and existing models. Here, we systematically dissect human pluripotent stem cell-derived osteoblasts to identify functional membrane proteins and their downstream transcriptional networks involved in human osteogenesis. Our results reveal an enrichment of type II transmembrane serine protease CORIN in humans but not rodent osteoblasts. Functional analyses demonstrated that CORIN depletion significantly impairs osteogenesis. Genome-wide chromatin immunoprecipitat</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-06-02T22:54:39.325Z</modification><creation>2024-11-09T02:03:44.016Z</creation></dates><accession>S-EPMC11301355</accession><cross_references><pubmed>38925326</pubmed><doi>10.1016/j.jbc.2024.107494</doi></cross_references></HashMap>