<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Q</submitter><funding>Education Department of Jiangxi Province</funding><pagination>605-614</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8102600</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>53(4)</volume><pubmed_abstract>The adult pancreatic ductal system was suggested to harbor facultative beta-cell progenitors similar to the embryonic pancreas, and the appearance of insulin-positive duct cells has been used as evidence for natural duct-to-beta-cell reprogramming. Nevertheless, the phenotype and fate of these insulin-positive cells in ducts have not been determined. Here, we used a cell-tagging dye, CFDA-SE, to permanently label pancreatic duct cells through an intraductal infusion technique. Representing a time when significant increases in beta-cell mass occur, pregnancy was later induced in these CFDA-SE-treated mice to assess the phenotype and fate of the insulin-positive cells in ducts. We found that a small portion of CFDA-SE-labeled duct cells became insulin-positive, but they were not fully functi</pubmed_abstract><journal>Experimental &amp; molecular medicine</journal><pubmed_title>Insulin-positive ductal cells do not migrate into preexisting islets during pregnancy.</pubmed_title><pmcid>PMC8102600</pmcid><funding_grant_id>GJJ180021</funding_grant_id><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Qian J</pubmed_authors><pubmed_authors>Zhu L</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Xiao X</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Gittes GK</pubmed_authors><pubmed_authors>Yang T</pubmed_authors><pubmed_authors>Prasadan K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Insulin-positive ductal cells do not migrate into preexisting islets during pregnancy.</name><description>The adult pancreatic ductal system was suggested to harbor facultative beta-cell progenitors similar to the embryonic pancreas, and the appearance of insulin-positive duct cells has been used as evidence for natural duct-to-beta-cell reprogramming. Nevertheless, the phenotype and fate of these insulin-positive cells in ducts have not been determined. Here, we used a cell-tagging dye, CFDA-SE, to permanently label pancreatic duct cells through an intraductal infusion technique. Representing a time when significant increases in beta-cell mass occur, pregnancy was later induced in these CFDA-SE-treated mice to assess the phenotype and fate of the insulin-positive cells in ducts. We found that a small portion of CFDA-SE-labeled duct cells became insulin-positive, but they were not fully functi</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2026-04-16T13:43:19.959Z</modification><creation>2022-02-10T11:43:28.823Z</creation></dates><accession>S-EPMC8102600</accession><cross_references><pubmed>33820959</pubmed><doi>10.1038/s12276-021-00593-z</doi></cross_references></HashMap>