| Literature DB >> 27923766 |
Damian Wollny1, Sheng Zhao1, Isabelle Everlien1, Xiaokang Lun1, Jan Brunken1, Daniel Brüne1, Frederik Ziebell2, Inna Tabansky3, Wilko Weichert4, Anna Marciniak-Czochra5, Ana Martin-Villalba6.
Abstract
Acinar cells make up the majority of all cells in the pancreas, yet the source of new acinar cells during homeostasis remains unknown. Using multicolor lineage-tracing and organoid-formation assays, we identified the presence of a progenitor-like acinar cell subpopulation. These cells have long-term self-renewal capacity, albeit in a unipotent fashion. We further demonstrate that binuclear acinar cells are terminally differentiated acinar cells. Transcriptome analysis of single acinar cells revealed the existence of a minor population of cells expressing progenitor markers. Interestingly, a gain of the identified markers accompanied by a transient gain of proliferation was observed following chemically induced pancreatitis. Altogether, our study identifies a functionally and molecularly distinct acinar subpopulation and thus transforms our understanding of the acinar cell compartment as a pool of equipotent secretory cells.Entities:
Keywords: acinar cells; multicolor lineage tracing; organoids; pancreas; progenitors; single-cell sequencing
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Year: 2016 PMID: 27923766 DOI: 10.1016/j.devcel.2016.10.002
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270