Department of Endocrinology and Metabolism, Shanghai Clinical Center for Diabetes, Shanghai Key Clinical Center for Metabolic Disease, Shanghai Diabetes Institute, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Department of Geriatrics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Front Endocrinol (Lausanne). 2021 Jan 11;11:592154. doi: 10.3389/fendo.2020.592154. eCollection 2020.
Mitochondrial iron-sulfur (Fe-S) cluster is an important cofactor for the maturation of Fe-S proteins, which are ubiquitously involved in energy metabolism; however, factors facilitating this process in beige fat have not been established. Here, we identified BolA family member 3 (Bola3), as one of 17 mitochondrial Fe-S cluster assembly genes, was the most significant induced gene in the browning program of white adipose tissue. Using lentiviral-delivered shRNA , we determined that Bola3 deficiency inhibited thermogenesis activity without affecting lipogenesis in differentiated beige adipocytes. The inhibition effect of Bola3 knockdown might be through impairing mitochondrial homeostasis and lipolysis. This was evidenced by the decreased expression of mitochondria related genes and respiratory chain complexes, attenuated mitochondrial formation, reduced mitochondrial maximal respiration and inhibited isoproterenol-stimulated lipolysis. Furthermore, BOLA3 mRNA levels were higher in human deep neck brown fat than in the paired subcutaneous white fat, and were positively correlated with thermogenesis related genes (UCP1, CIDEA, PRDM16, PPARG, COX7A1, and LIPE) expression in human omental adipose depots. This study demonstrates that Bola3 is associated with adipose tissue oxidative capacity both in mice and human, and it plays an indispensable role in beige adipocyte thermogenesis maintaining mitochondrial homeostasis and adrenergic signaling-induced lipolysis.
线粒体铁硫(Fe-S)簇是 Fe-S 蛋白成熟的重要辅助因子,这些蛋白广泛参与能量代谢;然而,在米色脂肪中促进这一过程的因素尚未确定。在这里,我们鉴定了 BolA 家族成员 3(Bola3),作为 17 种线粒体 Fe-S 簇组装基因之一,是白色脂肪组织棕色化程序中诱导表达最显著的基因之一。使用慢病毒递送的 shRNA,我们确定 Bola3 缺陷抑制了褐色脂肪细胞分化过程中的产热活性,而不影响脂生成。Bola3 敲低的抑制作用可能是通过损害线粒体稳态和脂解来实现的。这可以通过下调与线粒体相关的基因和呼吸链复合物的表达、减弱线粒体形成、减少线粒体最大呼吸和抑制异丙肾上腺素刺激的脂解来证明。此外,人深颈棕色脂肪中的 BOLA3 mRNA 水平高于配对的皮下白色脂肪,并且与人网膜脂肪组织中与产热相关的基因(UCP1、CIDEA、PRDM16、PPARG、COX7A1 和 LIPE)的表达呈正相关。这项研究表明,Bola3 与小鼠和人类的脂肪组织氧化能力有关,它在米色脂肪细胞产热中发挥不可或缺的作用,维持线粒体稳态和肾上腺素能信号诱导的脂解。