<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Y</submitter><funding>NICHD NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>1113-1126.e6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11890119</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(8)</volume><pubmed_abstract>Emerging human pluripotent stem cell (hPSC)-based embryo models are useful for studying human embryogenesis. Particularly, there are hPSC-based somitogenesis models using free-floating culture that recapitulate somite formation. Somitogenesis in vivo involves intricately orchestrated biochemical and biomechanical events. However, none of the current somitogenesis models controls biochemical gradients or biomechanical signals in the culture, limiting their applicability to untangle complex biochemical-biomechanical interactions that drive somitogenesis. Herein, we develop a human somitogenesis model by confining hPSC-derived presomitic mesoderm (PSM) tissues in microfabricated trenches. Exogenous microfluidic morphogen gradients imposed on the PSM tissues cause axial patterning and trigger </pubmed_abstract><journal>Cell stem cell</journal><pubmed_title>A human pluripotent stem cell-based somitogenesis model using microfluidics.</pubmed_title><pmcid>PMC11890119</pmcid><funding_grant_id>R01 NS129850</funding_grant_id><funding_grant_id>R21 NS127983</funding_grant_id><funding_grant_id>R21 NS113518</funding_grant_id><funding_grant_id>R21 HD105192</funding_grant_id><funding_grant_id>R01 HD085121</funding_grant_id><funding_grant_id>R21 HD109635</funding_grant_id><funding_grant_id>R21 HD105126</funding_grant_id><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Sun S</pubmed_authors><pubmed_authors>Fu J</pubmed_authors><pubmed_authors>Miao Y</pubmed_authors><pubmed_authors>Yan RZ</pubmed_authors><pubmed_authors>Yang Q</pubmed_authors><pubmed_authors>Kobayashi N</pubmed_authors><pubmed_authors>Kim YS</pubmed_authors><pubmed_authors>Xue X</pubmed_authors><pubmed_authors>Pourquie O</pubmed_authors></additional><is_claimable>false</is_claimable><name>A human pluripotent stem cell-based somitogenesis model using microfluidics.</name><description>Emerging human pluripotent stem cell (hPSC)-based embryo models are useful for studying human embryogenesis. Particularly, there are hPSC-based somitogenesis models using free-floating culture that recapitulate somite formation. Somitogenesis in vivo involves intricately orchestrated biochemical and biomechanical events. However, none of the current somitogenesis models controls biochemical gradients or biomechanical signals in the culture, limiting their applicability to untangle complex biochemical-biomechanical interactions that drive somitogenesis. Herein, we develop a human somitogenesis model by confining hPSC-derived presomitic mesoderm (PSM) tissues in microfabricated trenches. Exogenous microfluidic morphogen gradients imposed on the PSM tissues cause axial patterning and trigger </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-03-16T03:32:49.46Z</modification><creation>2025-08-14T03:05:42.139Z</creation></dates><accession>S-EPMC11890119</accession><cross_references><pubmed>38981471</pubmed><doi>10.1016/j.stem.2024.06.004</doi></cross_references></HashMap>