A mitochondrial UPR-mediated metabolic checkpoint regulates hematopoietic stem cell aging

Author:

Mohrin Mary1,Shin Jiyung1,Liu Yufei2,Brown Katharine1,Luo Hanzhi1,Xi Yannan1,Haynes Cole M.34,Chen Danica1

Affiliation:

1. Program in Metabolic Biology, Nutritional Sciences and Toxicology, University of California, Berkeley, CA 94720, USA.

2. Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.

3. Cell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

4. Biochemistry, Cell and Molecular Biology Allied Program, Weill Cornell Medical College, 1300 York Avenue, New York, NY, USA.

Abstract

Keeping stem cells in tip top condition Stem cells are important in the maintenance and growth of tissues. For the health of the organism as a whole, it is important that only healthy stem cells be used. Mohrin et al. elucidated a regulatory branch of the mitochondrial unfolded protein response that is coupled to cellular energy metabolism and proliferation in stem cells (see the Perspective by Ocampo and Belmonte). Mitochondrial protein folding stress triggered a metabolic checkpoint that regulates the cell cycle. Deregulation of this pathway interfered with stem cell quiescence and compromised regenerative function. Science , this issue p. 1374 ; see also p. 1319

Funder

NIH

Ellison Medical Foundation

Glenn Foundation

NSF Graduate Research Fellowship Program

Siebel Stem Cell Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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