AI Article Synopsis

  • High-fat diets (HFD) increase the number and activity of intestinal stem cells (specifically Lgr5(+) cells) in mammals, affecting their function.
  • The mechanism involves activation of peroxisome proliferator-activated receptor delta (PPAR-δ), which plays a key role in regulating these stem and progenitor cells.
  • PPAR-δ activation, whether through HFD or pharmacological means, not only boosts self-renewal in stem cells but also allows progenitor cells to form tumors when combined with loss of the Apc tumor suppressor gene.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846772PMC
http://dx.doi.org/10.1038/nature17173DOI Listing

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