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CLK1 和 PKCβII 抑制分子在 3T3-L1 细胞中诱导 beige 样脂肪细胞标志物和功能。

Induction of beige-like adipocyte markers and functions in 3T3-L1 cells by Clk1 and PKCβII inhibitory molecules.

机构信息

Department of Molecular Medicine, University of South Florida Morsani College of Medicine, Tampa, Florida, USA.

J.A. Haley Research Service, Tampa, Florida, USA.

出版信息

J Cell Mol Med. 2022 Aug;26(15):4183-4194. doi: 10.1111/jcmm.17345. Epub 2022 Jul 8.

Abstract

Excessive dietary intake of fat results in its storage in white adipose tissue (WAT). Energy expenditure through lipid oxidation occurs in brown adipose tissue (BAT). Certain WAT depots can undergo a change termed beiging where markers that BAT express are induced. Little is known about signalling pathways inducing beiging. Here, inhibition of a signalling pathway regulating alternative pre-mRNA splicing is involved in adipocyte beiging. Clk1/2/4 kinases regulate splicing by phosphorylating factors that process pre-mRNA. Clk1 inhibition by TG003 results in beige-like adipocytes highly expressing PGC1α and UCP1. SiRNA for Clk1, 2 and 4, demonstrated that Clk1 depletion increased UCP1 and PGC1α expression, whereas Clk2/4 siRNA did not. TG003-treated adipocytes contained fewer lipid droplets, are smaller, and contain more mitochondria, resulting in proton leak increases. Additionally, inhibition of PKCβII activity, a splice variant regulated by Clk1, increased beiging. PGC1α is a substrate for both Clk1 and PKCβII kinases, and we surmised that inhibition of PGC1α phosphorylation resulted in beiging of adipocytes. We show that TG003 binds Clk1 more than Clk2/4 through direct binding, and PGC1α binds to Clk1 at a site close to TG003. Furthermore, we show that TG003 is highly specific for Clk1 across hundreds of kinases in our activity screen. Hence, Clk1 inhibition becomes a target for induction of beige adipocytes.

摘要

过量的脂肪摄入会导致其在白色脂肪组织(WAT)中储存。棕色脂肪组织(BAT)通过脂质氧化来消耗能量。某些 WAT 可以发生一种称为“褐色化”的变化,即诱导 BAT 表达的标志物。目前对于诱导褐色化的信号通路知之甚少。在这里,调节替代前体 mRNA 剪接的信号通路的抑制参与了脂肪细胞的褐色化。CLK1/2/4 激酶通过磷酸化处理前体 mRNA 的因子来调节剪接。CLK1 的抑制物 TG003 导致高度表达 PGC1α 和 UCP1 的米色样脂肪细胞。CLK1、2 和 4 的 siRNA 表明,CLK1 耗竭增加了 UCP1 和 PGC1α 的表达,而 Clk2/4 siRNA 则没有。TG003 处理的脂肪细胞含有较少的脂滴,体积较小,含有更多的线粒体,导致质子泄漏增加。此外,Clk1 调节的剪接变异体 PKCβII 活性的抑制增加了褐色化。PGC1α 是 Clk1 和 PKCβII 激酶的底物,我们推测抑制 PGC1α 磷酸化导致脂肪细胞褐色化。我们表明,通过直接结合,TG003 与 Clk1 的结合比 Clk2/4 更多,并且 PGC1α 在靠近 TG003 的位点与 Clk1 结合。此外,我们表明,在我们的活性筛选中,TG003 在数百种激酶中对 Clk1 具有高度特异性。因此,CLK1 的抑制成为诱导米色脂肪细胞的一个靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077f/9344812/fba5952ab4ea/JCMM-26-4183-g003.jpg

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