| Literature DB >> 28768179 |
Nahid A Khan1, Joni Nikkanen1, Shuichi Yatsuga2, Christopher Jackson1, Liya Wang3, Swagat Pradhan1, Riikka Kivelä4, Alberto Pessia5, Vidya Velagapudi5, Anu Suomalainen6.
Abstract
Mitochondrial dysfunction elicits various stress responses in different model systems, but how these responses relate to each other and contribute to mitochondrial disease has remained unclear. Mitochondrial myopathy (MM) is the most common manifestation of adult-onset mitochondrial disease and shows a multifaceted tissue-specific stress response: (1) transcriptional response, including metabolic cytokines FGF21 and GDF15; (2) remodeling of one-carbon metabolism; and (3) mitochondrial unfolded protein response. We show that these processes are part of one integrated mitochondrial stress response (ISRmt), which is controlled by mTORC1 in muscle. mTORC1 inhibition by rapamycin downregulated all components of ISRmt, improved all MM hallmarks, and reversed the progression of even late-stage MM, without inducing mitochondrial biogenesis. Our evidence suggests that (1) chronic upregulation of anabolic pathways contributes to MM progression, (2) long-term induction of ISRmt is not protective for muscle, and (3) rapamycin treatment trials should be considered for adult-type MM with raised FGF21.Entities:
Keywords: ATF4; folate cycle; integrated mitochondrial stress response; mitochondrial disease; mitochondrial disease treatment; mitochondrial myopathy; nucleotide synthesis; one-carbon cycle; rapamycin; serine biosynthesis
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Year: 2017 PMID: 28768179 DOI: 10.1016/j.cmet.2017.07.007
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287