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Hasan, S.S.* ; Jabs, M.* ; Taylor, J.* ; Wiedmann, L.* ; Leibing, T.* ; Nordström, V.* ; Federico, G.* ; Roma, L.P.* ; Carlein, C.* ; Wolff, G. ; Ekim-Üstünel, B. ; Brune, M.* ; Moll, I.* ; Tetzlaff, F.* ; Gröne, H.J.* ; Fleming, T.* ; Géraud, C.* ; Herzig, S. ; Nawroth, P.P. ; Fischer, A.*

Endothelial Notch signaling controls insulin transport in muscle.

EMBO Mol. Med. 12:e09271 (2020)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
The role of the endothelium is not just limited to acting as an inert barrier for facilitating blood transport. Endothelial cells (ECs), through expression of a repertoire of angiocrine molecules, regulate metabolic demands in an organ-specific manner. Insulin flux across the endothelium to muscle cells is a rate-limiting process influencing insulin-mediated lowering of blood glucose. Here, we demonstrate that Notch signaling in ECs regulates insulin transport to muscle. Notch signaling activity was higher in ECs isolated from obese mice compared to non-obese. Sustained Notch signaling in ECs lowered insulin sensitivity and increased blood glucose levels. On the contrary, EC-specific inhibition of Notch signaling increased insulin sensitivity and improved glucose tolerance and glucose uptake in muscle in a high-fat diet-induced insulin resistance model. This was associated with increased transcription of Cav1, Cav2, and Cavin1, higher number of caveolae in ECs, and insulin uptake rates, as well as increased microvessel density. These data imply that Notch signaling in the endothelium actively controls insulin sensitivity and glucose homeostasis and may therefore represent a therapeutic target for diabetes.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Caveolae ; Endothelial Cell ; Insulin Transport ; Muscle ; Notch Signaling; Diet-induced Obesity; Skeletal-muscle; Microvascular Permeability; Caveolin-1; Delivery; Capillaries; Inhibition; Expression; Mice
Sprache englisch
Veröffentlichungsjahr 2020
HGF-Berichtsjahr 2020
ISSN (print) / ISBN 1757-4676
e-ISSN 1757-4684
Zeitschrift EMBO Molecular Medicine
Quellenangaben Band: 12, Heft: 4, Seiten: , Artikelnummer: e09271 Supplement: ,
Verlag Wiley
Verlagsort Chichester
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Diabetes and Cancer (IDC)
POF Topic(s) 90000 - German Center for Diabetes Research
Forschungsfeld(er) Helmholtz Diabetes Center
PSP-Element(e) G-501900-251
DOI 10.15252/emmm.201809271
WOS ID WOS:000520271300001
Scopus ID 85081980950
PubMed ID 32187826
WOS ID WOS:000526640800013
Erfassungsdatum 2020-04-16
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