4.8 Article

Region-Specific Proteome Changes of the Intestinal Epithelium during Aging and Dietary Restriction

期刊

CELL REPORTS
卷 31, 期 4, 页码 -

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2020.107565

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资金

  1. FLI Core Facilities Proteomics, Imaging, and Histology
  2. Mouse Facility
  3. German Research Foundation (Deutsche Forschungsgemeinschaft [DFG]) via the Research Training Group ProMoAge [GRK 2155]
  4. Else Kroner-Fresenius-Stiftung [2019_A79]
  5. Deutsches Zentrum fur HerzKreislaufforschung [81X2800193]
  6. Federal Government of Germany
  7. State of Thuringia
  8. NIH [R00 AG045144, R01CA211184, R01CA034992, U54CA224068, K99 DK123407-01]
  9. German Research Foundation (DFG) [SFB1127 ChemBioSys]
  10. DFG within the collaborative research center PolyTarget

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The small intestine is responsible for nutrient absorption and one of the most important interfaces between the environment and the body. During aging, changes of the epithelium lead to food malabsorption and reduced barrier function, thus increasing disease risk. The drivers of these alterations remain poorly understood. Here, we compare the proteomes of intestinal crypts from mice across different anatomical regions and ages. We find that aging alters epithelial immunity, metabolism, and cell proliferation and is accompanied by region-dependent skewing in the cellular composition of the epithelium. Of note, short-term dietary restriction followed by refeeding partially restores the epithelium by promoting stem cell differentiation toward the secretory lineage. We identify Hmgcs2 (3-hydroxy-3-methylglutaryl-coenzyme A [CoA] synthetase 2), the rate-limiting enzyme for ketogenesis, as a modulator of stem cell differentiation that responds to dietary changes, and we provide an atlas of region- and age-dependent proteome changes of the small intestine.

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