High-fat diet enhances stemness and tumorigenicity of intestinal progenitors

高脂肪饮食增强肠道祖细胞的干性和致瘤性

阅读:3
作者:Semir Beyaz,Miyeko D Mana,Jatin Roper,Dmitriy Kedrin,Assieh Saadatpour,Sue-Jean Hong,Khristian E Bauer-Rowe,Michael E Xifaras,Adam Akkad,Erika Arias,Luca Pinello,Yarden Katz,Shweta Shinagare,Monther Abu-Remaileh,Maria M Mihaylova,Dudley W Lamming,Rizkullah Dogum,Guoji Guo,George W Bell,Martin Selig,G Petur Nielsen,Nitin Gupta,Cristina R Ferrone,Vikram Deshpande,Guo-Cheng Yuan,Stuart H Orkin,David M Sabatini ,Ömer H Yilmaz

Abstract

Little is known about how pro-obesity diets regulate tissue stem and progenitor cell function. Here we show that high-fat diet (HFD)-induced obesity augments the numbers and function of Lgr5(+) intestinal stem cells of the mammalian intestine. Mechanistically, a HFD induces a robust peroxisome proliferator-activated receptor delta (PPAR-δ) signature in intestinal stem cells and progenitor cells (non-intestinal stem cells), and pharmacological activation of PPAR-δ recapitulates the effects of a HFD on these cells. Like a HFD, ex vivo treatment of intestinal organoid cultures with fatty acid constituents of the HFD enhances the self-renewal potential of these organoid bodies in a PPAR-δ-dependent manner. Notably, HFD- and agonist-activated PPAR-δ signalling endow organoid-initiating capacity to progenitors, and enforced PPAR-δ signalling permits these progenitors to form in vivo tumours after loss of the tumour suppressor Apc. These findings highlight how diet-modulated PPAR-δ activation alters not only the function of intestinal stem and progenitor cells, but also their capacity to initiate tumours.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。