<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Thongsa-Ad U</submitter><funding>Ministry of Science and Technology of Thailand</funding><funding>Mahidol University</funding><funding>Ramathibodi Foundation</funding><funding>Faculty of Science, Mahidol University</funding><funding>National Research Council of Thailand</funding><pagination>60</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10910864</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The diarylheptanoid ASPP 049 has improved the quality of adult hematopoietic stem cell (HSC) expansion ex vivo through long-term reconstitution in animal models. However, its effect on hematopoietic regeneration from human induced pluripotent stem cells (hiPSCs) is unknown.&lt;h4>Method&lt;/h4>We utilized a defined cocktail of cytokines without serum or feeder followed by the supplementation of ASPP 049 to produce hematopoietic stem/progenitor cells (HSPCs). Flow cytometry and trypan blue exclusion analysis were used to identify nonadherent and adherent cells. Nonadherent cells were harvested to investigate the effect of ASPP 049 on multipotency using LTC-IC and CFU assays. Subsequently, the mechanism of action was explored through transcriptomic profiles, which were validated</pubmed_abstract><journal>Stem cell research &amp; therapy</journal><pubmed_title>Improving hematopoietic differentiation from human induced pluripotent stem cells by the modulation of Hippo signaling with a diarylheptanoid derivative.</pubmed_title><pmcid>PMC10910864</pmcid><funding_grant_id>the Central Instrument Facility (CIF)</funding_grant_id><funding_grant_id>the Science Achievement Scholarship of Thailand</funding_grant_id><funding_grant_id>MU’s Strategic Research Fund: fiscal year 2023</funding_grant_id><funding_grant_id>N41A660154</funding_grant_id><funding_grant_id>MU's Strategic Research Fund: fiscal year 2023</funding_grant_id><pubmed_authors>Wongpan A</pubmed_authors><pubmed_authors>Tong-Ngam P</pubmed_authors><pubmed_authors>Chukhan A</pubmed_authors><pubmed_authors>Tubsuwan A</pubmed_authors><pubmed_authors>Wongniam S</pubmed_authors><pubmed_authors>Hongeng S</pubmed_authors><pubmed_authors>Uppakara K</pubmed_authors><pubmed_authors>Pabuprappap W</pubmed_authors><pubmed_authors>Bhukhai K</pubmed_authors><pubmed_authors>Anurathapan U</pubmed_authors><pubmed_authors>Wongkummool W</pubmed_authors><pubmed_authors>Thongsa-Ad U</pubmed_authors><pubmed_authors>Chaiwijit P</pubmed_authors><pubmed_authors>Kulkeaw K</pubmed_authors><pubmed_authors>Singpant P</pubmed_authors><pubmed_authors>Chaiyakitpattana G</pubmed_authors><pubmed_authors>Suksamrarn A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Improving hematopoietic differentiation from human induced pluripotent stem cells by the modulation of Hippo signaling with a diarylheptanoid derivative.</name><description>&lt;h4>Background&lt;/h4>The diarylheptanoid ASPP 049 has improved the quality of adult hematopoietic stem cell (HSC) expansion ex vivo through long-term reconstitution in animal models. However, its effect on hematopoietic regeneration from human induced pluripotent stem cells (hiPSCs) is unknown.&lt;h4>Method&lt;/h4>We utilized a defined cocktail of cytokines without serum or feeder followed by the supplementation of ASPP 049 to produce hematopoietic stem/progenitor cells (HSPCs). Flow cytometry and trypan blue exclusion analysis were used to identify nonadherent and adherent cells. Nonadherent cells were harvested to investigate the effect of ASPP 049 on multipotency using LTC-IC and CFU assays. Subsequently, the mechanism of action was explored through transcriptomic profiles, which were validated</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-16T04:50:51.866Z</modification><creation>2025-04-06T17:15:23.208Z</creation></dates><accession>S-EPMC10910864</accession><cross_references><pubmed>38433217</pubmed><doi>10.1186/s13287-024-03686-4</doi></cross_references></HashMap>