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Bta-微核糖核酸-2400靶向小泛素样修饰蛋白1以影响牦牛前体脂肪细胞的增殖和分化。

Bta-miR-2400 Targets SUMO1 to Affect Yak Preadipocytes Proliferation and Differentiation.

作者信息

Zhang Yongfeng, Ma Lanhua, Gu Yarong, Chang Yongfang, Liang Chunnian, Guo Xian, Bao Pengjia, Chu Min, Ding Xuezhi, Yan Ping

机构信息

Key Laboratory of Yak Breeding Engineering Gansu Province, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730050, China.

State Key Laboratory of Grassland Agro-Ecosystems, College of Pastoral Agriculture Science and Technology, Lanzhou University, Lanzhou 730000, China.

出版信息

Biology (Basel). 2021 Sep 22;10(10):949. doi: 10.3390/biology10100949.

Abstract

Yak adipose tissue may have evolved a unique energy metabolism manner to accommodate the organism's seasonal growth rhythms. MiRNAs regulate multiple biological processes including systemic metabolism and energy homeostasis through post-transcriptional regulations. Rare reports have shown that miRNAs regulate lipid metabolism in domestic yaks. Therefore, we investigated the regulatory mechanisms of bta-miR-2400 in modulating yak preadipocytes proliferation and differentiation. We found that bta-miR-2400 was highly expressed in adipose tissue. Overexpression of bta-miR-2400 in yak preadipocytes significantly enhanced cell proliferation, increased the number of EdU fluorescence-stained cells, and promoted the expression of proliferation marker genes (, and ). Besides, overexpression of bta-miR-2400 repressed the expression of adipogenesis-related marker genes, and the content of cellular triglyceride was substantially reduced. Conversely, inhibition of bta-miR-2400 showed opposite effects compared to those of bta-miR-2400 overexpression in yak preadipocytes. Further, luciferase reporter assays revealed that SUMO1 is a target gene of bta-miR-2400, with bta-miR-2400 being able to down-regulate SUMO1 mRNA and protein expression. In conclusion, bta-miR-2400 regulates lipid metabolism and energy homeostasis in yak preadipocytes by directly targeting SUMO1 to promote cell proliferation and inhibit differentiation.

摘要

牦牛脂肪组织可能已经进化出一种独特的能量代谢方式,以适应机体的季节性生长节律。微小RNA(miRNA)通过转录后调控来调节包括全身代谢和能量稳态在内的多个生物学过程。鲜有报道表明miRNA对家牦牛的脂质代谢有调控作用。因此,我们研究了bta-miR-2400在调节牦牛前体脂肪细胞增殖和分化中的调控机制。我们发现bta-miR-2400在脂肪组织中高表达。在牦牛前体脂肪细胞中过表达bta-miR-2400可显著增强细胞增殖,增加EdU荧光染色细胞的数量,并促进增殖标记基因( 、 和 )的表达。此外,bta-miR-2400的过表达抑制了脂肪生成相关标记基因的表达,细胞内甘油三酯含量大幅降低。相反,在牦牛前体脂肪细胞中抑制bta-miR-2400与过表达bta-miR-2400相比表现出相反的效果。进一步的荧光素酶报告基因检测显示,SUMO1是bta-miR-2400的靶基因,bta-miR-2400能够下调SUMO1的mRNA和蛋白表达。总之,bta-miR-2400通过直接靶向SUMO1促进细胞增殖并抑制分化,从而调节牦牛前体脂肪细胞中的脂质代谢和能量稳态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4156/8533534/a5f1019251c2/biology-10-00949-g001.jpg

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