FAM210A: Implications in mitochondrial dynamics and metabolic health

Author:

Lou Han12,Xu Henghui12,Zhang Yong123

Affiliation:

1. 1 Department of Pharmacology, College of Pharmacy, and Department of Cardiology, the Second Affiliated Hospital, Harbin Medical University, Harbin Medical University , Harbin , China

2. 2 The State Key Laboratory of Frigid Zone Cardiovascular Diseases (SKLFZCD), and the Key Laboratory of CardiovascularMedicine Research, Ministry of Education , Harbin , China

3. 3 Research Unit of Noninfectious Chronic Diseases in Frigid Zone, Chinese Academy of Medical Sciences , 2019RU070 , Harbin , China

Abstract

Abstract Brown adipose tissue (BAT), crucial for mammalian thermoregulation and energy metabolism, boasts a dense concentration of mitochondria. As a vital cellular organelle, mitochondria undergo substantial remodeling in cold environments, playing a pivotal role in maintaining body temperature and energy balance[1]. Mitochondrial dynamics, particularly mitochondrial cristae remodeling, are key processes governing BAT functionality. A recent study by Qiu et al. unveils groundbreaking insights, highlighting the significance of FAM210A (family with sequence similarity 210 member A) in orchestrating cold-induced mitochondrial remodeling in brown adipocytes. This research sheds light on the molecular mechanisms underpinning mitochondrial adaptability in cold environments[2]. Central to these discoveries is the protein FAM210A, recognized as a critical regulator of mitochondrial cristae remodeling in BAT. This revelation introduces new perspectives on metabolic regulation and thermogenic adaptation. This editorial aims to dissect these findings, extrapolating their broader implications for understanding metabolic health. Additionally, it explores potential therapeutic targets and discusses future directions in mitochondrial research.

Publisher

Walter de Gruyter GmbH

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