Mitochondrial matrix protein LETMD1 maintains thermogenic capacity of brown adipose tissue in male mice

Author:

Park Anna,Kim Kwang-eun,Park Isaac,Lee Sang Heon,Park Kun-YoungORCID,Jung Minkyo,Li Xiaoxu,Sleiman Maroun BouORCID,Lee Su Jeong,Kim Dae-SooORCID,Kim Jaehoon,Lim Dae-SikORCID,Woo Eui-JeonORCID,Lee Eun WooORCID,Han Baek Soo,Oh Kyoung-JinORCID,Lee Sang Chul,Auwerx JohanORCID,Mun Ji Young,Rhee Hyun-WooORCID,Kim Won KonORCID,Bae Kwang-HeeORCID,Suh Jae MyoungORCID

Abstract

AbstractBrown adipose tissue (BAT) has abundant mitochondria with the unique capability of generating heat via uncoupled respiration. Mitochondrial uncoupling protein 1 (UCP1) is activated in BAT during cold stress and dissipates mitochondrial proton motive force generated by the electron transport chain to generate heat. However, other mitochondrial factors required for brown adipocyte respiration and thermogenesis under cold stress are largely unknown. Here, we show LETM1 domain-containing protein 1 (LETMD1) is a BAT-enriched and cold-induced protein required for cold-stimulated respiration and thermogenesis of BAT. Proximity labeling studies reveal that LETMD1 is a mitochondrial matrix protein. Letmd1 knockout male mice display aberrant BAT mitochondria and fail to carry out adaptive thermogenesis under cold stress. Letmd1 knockout BAT is deficient in oxidative phosphorylation (OXPHOS) complex proteins and has impaired mitochondrial respiration. In addition, BAT-specific Letmd1 deficient mice exhibit phenotypes identical to those observed in Letmd1 knockout mice. Collectively, we demonstrate that the BAT-enriched mitochondrial matrix protein LETMD1 plays a tissue-autonomous role that is essential for BAT mitochondrial function and thermogenesis.

Funder

Korea Research Institute of Bioscience and Biotechnology

National Research Foundation of Korea

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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