<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ji SF</submitter><funding>the National Natural Science Foundation of China</funding><pagination>13</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8962256</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Large skin defects severely disrupt the overall skin structure and can irreversibly damage sweat glands (SG), thus impairing the skin's physiological function. This study aims to develop a stepwise reprogramming strategy to convert fibroblasts into SG lineages, which may provide a promising method to obtain desirable cell types for the functional repair and regeneration of damaged skin.&lt;h4>Methods&lt;/h4>The expression of the SG markers cytokeratin 5 (CK5), cytokeratin 10 (CK10), cytokeratin 18 (CK18), carcino-embryonic antigen (CEA), aquaporin 5 (AQP5) and α-smooth muscle actin (α-SMA) was assessed with quantitative PCR (qPCR), immunofluorescence and flow cytometry. Calcium activity analysis was conducted to test the function of induced SG-like cells (iSGCs). Mouse xenogra</pubmed_abstract><journal>Military Medical Research</journal><pubmed_title>Small molecules facilitate single factor-mediated sweat gland cell reprogramming.</pubmed_title><pmcid>PMC8962256</pmcid><funding_grant_id>81871569</funding_grant_id><pubmed_authors>Sun XY</pubmed_authors><pubmed_authors>Zhou LX</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Sun ZF</pubmed_authors><pubmed_authors>Chen HT</pubmed_authors><pubmed_authors>Xiang JB</pubmed_authors><pubmed_authors>Ji SF</pubmed_authors><pubmed_authors>Cui SY</pubmed_authors><pubmed_authors>Gao HH</pubmed_authors><pubmed_authors>Fu XB</pubmed_authors><pubmed_authors>Liu YQ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Small molecules facilitate single factor-mediated sweat gland cell reprogramming.</name><description>&lt;h4>Background&lt;/h4>Large skin defects severely disrupt the overall skin structure and can irreversibly damage sweat glands (SG), thus impairing the skin's physiological function. This study aims to develop a stepwise reprogramming strategy to convert fibroblasts into SG lineages, which may provide a promising method to obtain desirable cell types for the functional repair and regeneration of damaged skin.&lt;h4>Methods&lt;/h4>The expression of the SG markers cytokeratin 5 (CK5), cytokeratin 10 (CK10), cytokeratin 18 (CK18), carcino-embryonic antigen (CEA), aquaporin 5 (AQP5) and α-smooth muscle actin (α-SMA) was assessed with quantitative PCR (qPCR), immunofluorescence and flow cytometry. Calcium activity analysis was conducted to test the function of induced SG-like cells (iSGCs). Mouse xenogra</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-06-20T04:51:38.309Z</modification><creation>2025-04-06T15:49:27.761Z</creation></dates><accession>S-EPMC8962256</accession><cross_references><pubmed>35351192</pubmed><doi>10.1186/s40779-022-00372-5</doi></cross_references></HashMap>