Single-Cell Analysis Uncovers Clonal Acinar Cell Heterogeneity in the Adult Pancreas

被引:84
作者
Wollny, Damian [1 ]
Zhao, Sheng [1 ]
Everlien, Isabelle [1 ]
Lun, Xiaokang [1 ,5 ]
Brunken, Jan [1 ]
Bruene, Daniel [1 ]
Ziebell, Frederik [1 ,2 ]
Tabansky, Inna [3 ]
Weichert, Wilko [4 ]
Marciniak-Czochra, Anna [2 ]
Martin-Villalba, Ana [1 ]
机构
[1] German Canc Res Ctr, Mol Neurobiol, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, Inst Appl Math, D-69120 Heidelberg, Germany
[3] Rockefeller Univ, Dept Neurobiol & Behav, 1230 York Ave, New York, NY 10065 USA
[4] Tech Univ Munich, Inst Pathol, D-81675 Munich, Germany
[5] Univ Zurich, Inst Mol Life Sci, CH-8057 Zurich, Switzerland
关键词
RNA-SEQ; GENERATION; PLASTICITY; HEPATOCYTES; PROGENITORS; HOMEOSTASIS; COLONIES; GROWTH;
D O I
10.1016/j.devcel.2016.10.002
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
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.
引用
收藏
页码:289 / 301
页数:13
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