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高脂饮食增强肠道祖细胞的干性和致瘤性。

High-fat diet enhances stemness and tumorigenicity of intestinal progenitors.

作者信息

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

机构信息

The David H. Koch Institute for Integrative Cancer Research at MIT, Department of Biology, MIT, Cambridge, Massachusetts 02139, USA.

Division of Hematology/Oncology, Boston Children's Hospital and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Howard Hughes Medical Institute, Harvard Stem Cell Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Nature. 2016 Mar 3;531(7592):53-8. doi: 10.1038/nature17173.

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.

摘要

关于致肥胖饮食如何调节组织干细胞和祖细胞功能,人们了解甚少。在此我们表明,高脂饮食(HFD)诱导的肥胖会增加哺乳动物肠道中Lgr5(+)肠干细胞的数量和功能。从机制上来说,高脂饮食会在肠干细胞和祖细胞(非肠干细胞)中诱导强烈的过氧化物酶体增殖物激活受体δ(PPAR-δ)信号特征,PPAR-δ的药理学激活模拟了高脂饮食对这些细胞的影响。与高脂饮食一样,用高脂饮食的脂肪酸成分对肠道类器官培养物进行体外处理,以PPAR-δ依赖的方式增强了这些类器官体的自我更新潜力。值得注意的是,高脂饮食和激动剂激活的PPAR-δ信号赋予祖细胞类器官起始能力,并且在肿瘤抑制因子Apc缺失后,增强的PPAR-δ信号使这些祖细胞能够在体内形成肿瘤。这些发现突出了饮食调节的PPAR-δ激活不仅如何改变肠干细胞和祖细胞的功能,还改变了它们起始肿瘤的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f9/4846772/fdd3aba37abf/nihms755851f6.jpg

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