Metabolic flexibility via mitochondrial BCAA carrier SLC25A44 is required for optimal fever.

Journal Article (Journal Article)

Importing necessary metabolites into the mitochondrial matrix is a crucial step of fuel choice during stress adaptation. Branched chain-amino acids (BCAAs) are essential amino acids needed for anabolic processes, but they are also imported into the mitochondria for catabolic reactions. What controls the distinct subcellular BCAA utilization during stress adaptation is insufficiently understood. The present study reports the role of SLC25A44, a recently identified mitochondrial BCAA carrier (MBC), in the regulation of mitochondrial BCAA catabolism and adaptive response to fever in rodents. We found that mitochondrial BCAA oxidation in brown adipose tissue (BAT) is significantly enhanced during fever in response to the pyrogenic mediator prostaglandin E2 (PGE2) and psychological stress in mice and rats. Genetic deletion of MBC in a BAT-specific manner blunts mitochondrial BCAA oxidation and non-shivering thermogenesis following intracerebroventricular PGE2 administration. At a cellular level, MBC is required for mitochondrial BCAA deamination as well as the synthesis of mitochondrial amino acids and TCA intermediates. Together, these results illuminate the role of MBC as a determinant of metabolic flexibility to mitochondrial BCAA catabolism and optimal febrile responses. This study also offers an opportunity to control fever by rewiring the subcellular BCAA fate.

Full Text

Duke Authors

Cited Authors

  • Yoneshiro, T; Kataoka, N; Walejko, JM; Ikeda, K; Brown, Z; Yoneshiro, M; Crown, SB; Osawa, T; Sakai, J; McGarrah, RW; White, PJ; Nakamura, K; Kajimura, S

Published Date

  • May 4, 2021

Published In

Volume / Issue

  • 10 /

PubMed ID

  • 33944778

Pubmed Central ID

  • PMC8137140

Electronic International Standard Serial Number (EISSN)

  • 2050-084X

Digital Object Identifier (DOI)

  • 10.7554/eLife.66865

Language

  • eng

Conference Location

  • England