Roshanzadeh Amir, Yadav Anil Kumar, Pydi Sai-Prasad, Kimura Takefumi, Jang Byeong-Churl
Department of Molecular Medicine, College of Medicine, Keimyung University, 1095 Dalgubeoldaero, Dalseo-gu, Daegu 42601, Korea.
The Hormel Institute, University of Minnesota, Austin, MN 55912, USA.
Biology (Basel). 2022 May 18;11(5):772. doi: 10.3390/biology11050772.
β3-adrenergic receptor (β3-AR) is expressed predominantly in mature white and brown/beige adipocytes. Although the lipolytic and thermogenic role of β3-AR in brown/beige adipocytes is well defined, the adipogenic role of β3-AR in white adipocytes remains unclear at present. In this study, we investigated the expression and function of β3-AR in differentiating 3T3-L1 cells, murine white preadipocytes. Of note, the expression of β3-AR at the protein and mRNA levels was highly induced in a time-dependent manner during 3T3-L1 preadipocyte differentiation. Interestingly, the results of the pharmacological inhibition study demonstrated the roles of p38 MAPK and PKC in the induction of β3-AR expression in differentiating 3T3-L1 cells. Knockdown of β3-AR led to less lipid accumulation and triglyceride (TG) content during 3T3-L1 preadipocyte differentiation with no cytotoxicity. Furthermore, knockdown of β3-AR resulted in a decrease in not only expression levels of CCAAT/enhancer-binding protein-α (C/EBP-α), peroxisome proliferator-activated receptor-γ (PPAR-γ), fatty acid synthase (FASN), perilipin A, and leptin but also phosphorylation levels of signal transducer and activator of transcription-5 (STAT-5) during 3T3-L1 preadipocyte differentiation. In summary, these results demonstrate firstly that β3-AR expression is highly up-regulated in p38 MAPK and PKC-dependent manners, and the up-regulated β3-AR plays a crucial role in lipid accumulation in differentiating 3T3-L1 cells, which is mediated through control of expression and phosphorylation levels of C/EBP-α, PPAR-γ, STAT-5, FASN, and perilipin A.
β3肾上腺素能受体(β3-AR)主要在成熟的白色和棕色/米色脂肪细胞中表达。尽管β3-AR在棕色/米色脂肪细胞中的脂解和产热作用已得到明确,但β3-AR在白色脂肪细胞中的成脂作用目前仍不清楚。在本研究中,我们调查了β3-AR在分化的3T3-L1细胞(小鼠白色前脂肪细胞)中的表达和功能。值得注意的是,在3T3-L1前脂肪细胞分化过程中,β3-AR的蛋白质和mRNA水平表达呈时间依赖性高度诱导。有趣的是,药理学抑制研究结果表明p38丝裂原活化蛋白激酶(p38 MAPK)和蛋白激酶C(PKC)在分化的3T3-L1细胞中诱导β3-AR表达中发挥作用。敲低β3-AR导致3T3-L1前脂肪细胞分化过程中脂质积累和甘油三酯(TG)含量减少,且无细胞毒性。此外,敲低β3-AR不仅导致3T3-L1前脂肪细胞分化过程中CCAAT/增强子结合蛋白-α(C/EBP-α)、过氧化物酶体增殖物激活受体-γ(PPAR-γ)、脂肪酸合酶(FASN)、围脂滴蛋白A和瘦素的表达水平降低,还导致信号转导和转录激活因子-5(STAT-5)的磷酸化水平降低。总之,这些结果首先证明β3-AR表达以p38 MAPK和PKC依赖性方式高度上调,上调的β3-AR在分化的3T3-L1细胞的脂质积累中起关键作用,这是通过控制C/EBP-α、PPAR-γ、STAT-5、FASN和围脂滴蛋白A的表达和磷酸化水平介导的。