The nuclear receptor FXR is expressed in pancreatic beta-cells and protects human islets from lipotoxicity.

Abstract:

:Farnesoid X receptor (FXR) is highly expressed in liver and intestine where it controls bile acid (BA), lipid and glucose homeostasis. Here we show that FXR is expressed and functional, as assessed by target gene expression analysis, in human islets and beta-cell lines. FXR is predominantly cytosolic-localized in the islets of lean mice, but nuclear in obese mice. Compared to FXR+/+ mice, FXR-/- mice display a normal architecture and beta-cell mass but the expression of certain islet-specific genes is altered. Moreover, glucose-stimulated insulin secretion (GSIS) is impaired in the islets of FXR-/- mice. Finally, FXR activation protects human islets from lipotoxicity and ameliorates their secretory index.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Popescu IR,Helleboid-Chapman A,Lucas A,Vandewalle B,Dumont J,Bouchaert E,Derudas B,Kerr-Conte J,Caron S,Pattou F,Staels B

doi

10.1016/j.febslet.2010.04.068

subject

Has Abstract

pub_date

2010-07-02 00:00:00

pages

2845-51

issue

13

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(10)00372-8

journal_volume

584

pub_type

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