@article{3650,
  keywords = {Animals, Mice, Transcription Factors, Chromatin Immunoprecipitation, Blotting, Western, Flow Cytometry, Homeostasis, Mass Spectrometry, DNA-Binding Proteins, Female, Male, Fluorescent Antibody Technique, Cell Differentiation, Stem Cells, Intestinal Mucosa},
  author = {Rachel Stine and Alexander Sakers and Tara TeSlaa and Megan Kissig and Zachary Stine and Chan Kwon and Lan Cheng and Hee-Woong Lim and Klaus Kaestner and Joshua Rabinowitz and Patrick Seale},
  title = {PRDM16 Maintains Homeostasis of the Intestinal Epithelium by Controlling Region-Specific Metabolism.},
  abstract = { <p>Metabolic pathways dynamically regulate tissue development and maintenance. However, the mechanisms that govern the metabolic adaptation of stem or progenitor cells to their local niche are poorly understood. Here, we define the transcription factor PRDM16 as a region-specific regulator of intestinal metabolism and epithelial renewal. PRDM16 is selectively expressed in the upper intestine, with enrichment in crypt-resident progenitor cells. Acute Prdm16 deletion in mice triggered progenitor apoptosis, leading to diminished epithelial differentiation and severe intestinal atrophy. Genomic and metabolic analyses showed that PRDM16 transcriptionally controls fatty acid oxidation (FAO) in crypts. Expression of this PRDM16-driven FAO program was highest in the upper small intestine and declined distally. Accordingly, deletion of Prdm16 or inhibition of FAO selectively impaired the development and maintenance of upper intestinal enteroids, and these effects were rescued by acetate treatment. Collectively, these data reveal that regionally specified metabolic programs regulate intestinal maintenance.</p> },
  year = {2019},
  journal = {Cell Stem Cell},
  volume = {25},
  pages = {830-845.e8},
  month = {2019 Dec 05},
  issn = {1875-9777},
  doi = {10.1016/j.stem.2019.08.017},
  language = {eng},
}