Wang Tianming, Zhang Tianyu, Tang Youzhi, Wang Hongshun, Wei Qinjun, Lu Yajie, Yao Jun, Qu Yuan, Cao Xin
Department of Medical Genetics, School of Basic Medical Science, Nanjing Medical University, Nanjing, China.
Jiangsu Cancer Hospital, Nanjing Medical University, Nanjing, China.
Cell Death Discov. 2021 May 17;7(1):109. doi: 10.1038/s41420-021-00503-2.
Oxysterol-binding protein-like 2 (OSBPL2), also known as oxysterol-binding protein-related protein (ORP) 2, is a member of lipid transfer protein well-known for its role in regulating cholesterol homeostasis. A recent study reported that OSBPL2/ORP2 localizes to lipid droplets (LDs) and is associated with energy metabolism and obesity. However, the function of OSBPL2/ORP2 in adipocyte differentiation is poorly understood. Here, we report that OSBPL2/ORP2 contributes to the developmental progression of preadipocytes. We found that OSBPL2/ORP2 binds to β-catenin, a key effector in the Wnt signaling pathway that inhibits adipogenesis. This complex plays a role in regulating the protein level of β-catenin only in preadipocytes, not in mature adipocytes. Our data further indicated that OSBPL2/ORP2 mediates the transport of β-catenin into the nucleus and thus regulates target genes related to adipocyte differentiation. Deletion of OSBPL2/ORP2 markedly reduces β-catenin both in the cytoplasm and in the nucleus, promotes preadipocytes maturation, and ultimately leads to obesity-related characteristics. Altogether, we provide novel insight into the function of OSBPL2/ORP2 in the developmental progression of preadipocytes and suggest OSBPL2/ORP2 may be a potential therapeutic target for the treatment of obesity-related diseases.
氧化甾醇结合蛋白样2(OSBPL2),也被称为氧化甾醇结合蛋白相关蛋白(ORP)2,是脂质转移蛋白家族的一员,因其在调节胆固醇稳态中的作用而闻名。最近一项研究报道,OSBPL2/ORP2定位于脂滴(LDs),并与能量代谢和肥胖相关。然而,人们对OSBPL2/ORP2在脂肪细胞分化中的功能了解甚少。在此,我们报道OSBPL2/ORP2有助于前脂肪细胞的发育进程。我们发现OSBPL2/ORP2与β-连环蛋白结合,β-连环蛋白是Wnt信号通路中抑制脂肪生成的关键效应因子。这种复合物仅在前脂肪细胞中对β-连环蛋白的蛋白水平起调节作用,而在成熟脂肪细胞中则不然。我们的数据进一步表明,OSBPL2/ORP2介导β-连环蛋白转运至细胞核,从而调节与脂肪细胞分化相关的靶基因。缺失OSBPL2/ORP2会显著降低细胞质和细胞核中的β-连环蛋白水平,促进前脂肪细胞成熟,并最终导致肥胖相关特征。总之,我们为OSBPL2/ORP2在前脂肪细胞发育进程中的功能提供了新的见解,并表明OSBPL2/ORP2可能是治疗肥胖相关疾病的潜在治疗靶点。