| Literature DB >> 33906911 |
Uylissa A Rodriguez1, Mairobys Socorro1,2, Angela Criscimanna1, Christina P Martins1, Nada Mohamed1, Jing Hu3, Krishna Prasadan1, George K Gittes1, Farzad Esni4,5,6.
Abstract
In contrast to the skin and the gut, where somatic stem cells and their niche are well characterized, a definitive pancreatic multipotent cell population in the adult pancreas has yet to be revealed. Of particular interest is whether such cells may be endogenous in patients with diabetes, and if so, can they be used for therapeutic purposes? In the current study, we used two separate reporter lines to target Cre-recombinase expression to the Lgr5- or glucagon-expressing cells in the pancreas. We provide evidence for the existence of a population of cells within and in the proximity of the ducts that transiently express the stem-cell marker Lgr5 during late gestational stages. Careful timing of tamoxifen treatment in Lgr5EGFP-IRES-CreERT2 ;R26 Tomato mice allowed us to show that these Lgr5-expressing progenitor cells can differentiate into α-cells during pregnancy. Furthermore, we report on a spontaneous lineage conversion of α- to β-cells specifically after parturition. The contribution of Lgr5 progeny to the β-cell compartment through an α-cell intermediate phase early after pregnancy appears to be part of a novel mechanism that would counterbalance against excessive β-cell mass reduction during β-cell involution.Entities:
Year: 2021 PMID: 33906911 DOI: 10.2337/db20-1059
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461