<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jeong YJ</submitter><funding>Yonsei University College of Medicine</funding><funding>Commercializations Promotion Agency for R and D Outcomes</funding><funding>Ministry of Science and ICT, South Korea</funding><pagination>187</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12008940</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Salivary gland (SG) hypofunction presents a significant clinical challenge with limited treatment options. SG epithelial cells offer a promising approach due to their intrinsic tissue specificity and regenerative potential. However, the lack of efficient culture methods has hindered their clinical use.&lt;h4>Methods&lt;/h4>This study presents a chemical reprogramming culture (CRC) system that utilizes a combination of three small molecules for the long-term two-dimensional culture of human SG epithelial progenitor cells. We characterized the cultured cells, measured their organoid-forming efficiencies, and assessed their differentiation potential. To evaluate the therapeutic efficacy of the SG basal progenitor cells (SG-BPCs), we administered them into a mouse model with radia</pubmed_abstract><journal>Stem cell research &amp; therapy</journal><pubmed_title>Chemical reprogramming culture for the expansion of salivary gland epithelial basal progenitor cells.</pubmed_title><pmcid>PMC12008940</pmcid><funding_grant_id>RS-2022-00164878</funding_grant_id><funding_grant_id>6-2022-0106</funding_grant_id><funding_grant_id>RS-2024-00432946</funding_grant_id><pubmed_authors>Hong SM</pubmed_authors><pubmed_authors>Hong Y</pubmed_authors><pubmed_authors>Sim NS</pubmed_authors><pubmed_authors>Lim JY</pubmed_authors><pubmed_authors>Jeong YJ</pubmed_authors><pubmed_authors>Yoon YJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chemical reprogramming culture for the expansion of salivary gland epithelial basal progenitor cells.</name><description>&lt;h4>Background&lt;/h4>Salivary gland (SG) hypofunction presents a significant clinical challenge with limited treatment options. SG epithelial cells offer a promising approach due to their intrinsic tissue specificity and regenerative potential. However, the lack of efficient culture methods has hindered their clinical use.&lt;h4>Methods&lt;/h4>This study presents a chemical reprogramming culture (CRC) system that utilizes a combination of three small molecules for the long-term two-dimensional culture of human SG epithelial progenitor cells. We characterized the cultured cells, measured their organoid-forming efficiencies, and assessed their differentiation potential. To evaluate the therapeutic efficacy of the SG basal progenitor cells (SG-BPCs), we administered them into a mouse model with radia</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2025-06-28T03:05:34.844Z</modification><creation>2025-06-28T03:05:34.844Z</creation></dates><accession>S-EPMC12008940</accession><cross_references><pubmed>40251601</pubmed><doi>10.1186/s13287-025-04295-5</doi></cross_references></HashMap>