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Mameishvili, E. ; Serafimidis, I.* ; Iwaszkiewicz, S. ; Lesche, M. ; Reinhardt, S.* ; Bölicke, N. ; Büttner, M. ; Stellas, D.* ; Papadimitropoulou, A.* ; Szabolcs, M.* ; Anastassiadis, K.* ; Dahl, A.* ; Theis, F.J. ; Efstratiadis, A.* ; Gavalas, A.

Aldh1b1 expression defines progenitor cells in the adult pancreas and is required for Kras-induced pancreatic cancer.

Proc. Natl. Acad. Sci. U.S.A. 116, 20679-20688 (2019)
Verlagsversion Postprint DOI PMC
Open Access Gold
The presence of progenitor or stem cells in the adult pancreas and their potential involvement in homeostasis and cancer development remain unresolved issues. Here, we show that mouse centroacinar cells can be identified and isolated by virtue of the mitochondrial enzyme Aldh1b1 that they uniquely express. These cells are necessary and sufficient for the formation of self-renewing adult pancreatic organoids in an Aldh1b1-dependent manner. Aldh1b1-expressing centroacinar cells are largely quiescent, self-renew, and, as shown by genetic lineage tracing, contribute to all 3 pancreatic lineages in the adult organ under homeostatic conditions. Single-cell RNA sequencing analysis of these cells identified a progenitor cell population, established its molecular signature, and determined distinct differentiation pathways to early progenitors. A distinct feature of these progenitor cells is the preferential expression of small GTPases, including Kras, suggesting that they might be susceptible to Kras-driven oncogenic transformation. This finding and the overexpression of Aldh1b1 in human and mouse pancreatic cancers, driven by activated Kras, prompted us to examine the involvement of Aldh1b1 in oncogenesis. We demonstrated genetically that ablation of Aldh1b1 completely abrogates tumor development in a mouse model of Kras(G12D)-induced pancreatic cancer.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Adult Stem And Progenitor Cells ; Aldehyde Dehydrogenase ; Organoids ; Single-cell Rna Sequencing ; Pancreatic Ductal Adenocarcinoma; Aldehyde Dehydrogenase 1b1; Beta-cells; Centroacinar Cells; Exocrine Cells; Oncogenic Kras; Acinar-cells; Ductal Cells; Stem-cells; Endocrine; Differentiation
Sprache englisch
Veröffentlichungsjahr 2019
HGF-Berichtsjahr 2019
ISSN (print) / ISBN 0027-8424
e-ISSN 1091-6490
Zeitschrift Proceedings of the National Academy of Sciences of the United States of America
Quellenangaben Band: 116, Heft: 41, Seiten: 20679-20688 Artikelnummer: , Supplement: ,
Verlag National Academy of Sciences
Verlagsort 2101 Constitution Ave Nw, Washington, Dc 20418 Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Pancreatic Islet Research (IPI)
Institute of Computational Biology (ICB)
POF Topic(s) 90000 - German Center for Diabetes Research
30205 - Bioengineering and Digital Health
Forschungsfeld(er) Helmholtz Diabetes Center
Enabling and Novel Technologies
PSP-Element(e) G-502600-003
G-503800-001
DOI 10.1073/pnas.1901075116
WOS ID WOS:000489770700063
Scopus ID 85073073758
PubMed ID 31548432
Erfassungsdatum 2019-09-26
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