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Gerst, F. ; Wagner, R. ; Oquendo, M.B.* ; Siegel-Axel, D.I.* ; Fritsche, A.* ; Heni, M. ; Staiger, H. ; Häring, H.-U. ; Ullrich, S.

What role do fat cells play in pancreatic tissue?

Mol. Metab. 25, 1-10 (2019)
Verlagsversion DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Background: It is now generally accepted that obesity is a major risk factor for type 2 diabetes mellitus (T2DM). Hepatic steatosis in particular, as well as visceral and ectopic fat accumulation within tissues, is associated with the development of the disease. We recently presented the first study on isolated human pancreatic adipocytes and their interaction with islets [Gerst, F., Wagner, R., Kaiser, G., Panse, M., Heni, M., Machann, J., et al., 2017. Metabolic crosstalk between fatty pancreas and fatty liver: effects on local inflammation and insulin secretion. Diabetologia 60(11): 2240-2251.]. The results indicate that the function of adipocytes depends on the overall metabolic status in humans which, in turn, differentially affects islet hormone release.Scope of Review: This review summarizes former and recent studies on factors derived from adipocytes and their effects on insulin-secreting beta-cells, with particular emphasis on the human pancreas. The adipocyte secretome is discussed with a special focus on its influence on insulin secretion, beta-cell survival and apoptotic beta-cell death.Major Conclusions: Human pancreatic adipocytes store lipids and release adipokines, metabolites, and pro-inflammatory molecules in response to the overall metabolic, humoral, and neuronal status. The differentially regulated adipocyte secretome impacts on endocrine function, i.e., insulin secretion, beta-cell survival and death which interferes with glycemic control. This review attempts to explain why the extent of pancreatic steatosis is associated with reduced insulin secretion in some studies but not in others. (C) 2019 The Authors. Published by Elsevier GmbH.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Fatty Pancreas ; Adipocytes ; Paracrine Signalling ; Insulin Secretion ; Beta-cell Mass ; Type 2 Diabetes Mellitus (t2dm); Stimulated Insulin-secretion; Endoplasmic-reticulum Stress; Acid-induced Apoptosis; Long-term Exposure; Beta-cell; Adipose-tissue; Metabolic Syndrome; In-vivo; Alpha-2-adrenergic Inhibition; Inflammatory Cytokines
Sprache
Veröffentlichungsjahr 2019
HGF-Berichtsjahr 2019
ISSN (print) / ISBN 2212-8778
e-ISSN 2212-8778
Zeitschrift Molecular Metabolism
Quellenangaben Band: 25, Heft: , Seiten: 1-10 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort Amsterdam
Begutachtungsstatus Peer reviewed
POF Topic(s) 90000 - German Center for Diabetes Research
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-502400-001
Scopus ID 85065796256
PubMed ID 31113756
Erfassungsdatum 2019-05-24