MiR-33a plays an crucial role in the proliferation of bovine preadipocytes.

IF 3.5 4区 生物学 Q2 ENDOCRINOLOGY & METABOLISM
Wenzhen Zhang, Li Wang, Sayed Haidar Abbas Raza, Xiaoyu Wang, Guohu Wang, Chengcheng Liang, Gong Cheng, Bingzhi Li, Linsen Zan
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引用次数: 0

Abstract

Preadipocyte proliferation is a critical and precisely orchestrated procedure in adipogenesis, which is highly regulated by microRNAs (miRNAs). A previous study identified that the expression of miR-33a is different in intramuscular fat (IMF) tissues from steers and bulls. In the present study, miR-33a was overexpressed in bovine preadipocytes, and a total of 781 differentialy expressed genes were found, including 348 upregulated and 433 downregulated genes. Gene Ontology and Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway analyses of the differentially expressed genes enriched cell division and cell cycle respectively. MiR-33a overexpression decreased the rate of preadipocyte proliferation. Synchronously, the mRNA and protein expression levels of proliferation-related marker genes, including cyclin B1 (CCNB1) and proliferating cell nuclear antigen (PCNA), were decreased. In contrast, inhibiting miR-33a increased the rate of preadipocyte proliferation, and expression levels of CCNB1 and PCNA. Furthermore, based on luciferase reporter assays, miR-33a targeted directly cyclin-dependent kinase 6 (CDK6)-3'UTR and inhibited CDK6 protein expression. Interestingly, the silencing of CDK6 inhibited bovine preadipocyte proliferation and proliferation-related genes. Therefore, miR-33a inhibits the proliferation of bovine preadipocytes. CDK6 is the target gene of miR-33a and may be involved in the effects of miR-33a on bovine preadipocyte proliferation.

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MiR-33a 在牛前脂肪细胞的增殖过程中起着至关重要的作用。
前脂肪细胞增殖是脂肪生成过程中的一个关键和精确协调的过程,它受到微RNA(miRNA)的高度调控。之前的一项研究发现,miR-33a 在母牛和公牛的肌内脂肪(IMF)组织中的表达不同。在本研究中,miR-33a 在牛前脂肪细胞中过表达,共发现 781 个差异表达基因,包括 348 个上调基因和 433 个下调基因。基因本体和京都基因组百科全书(KEGG)对差异表达基因进行了通路分析,发现细胞分裂和细胞周期的差异表达基因较多。MiR-33a的过表达降低了前脂肪细胞的增殖速度。与此同时,细胞周期蛋白 B1(CCNB1)和增殖细胞核抗原(PCNA)等增殖相关标记基因的 mRNA 和蛋白表达水平也下降了。相反,抑制 miR-33a 会增加前脂肪细胞的增殖速度以及 CCNB1 和 PCNA 的表达水平。此外,根据荧光素酶报告实验,miR-33a 直接靶向细胞周期蛋白依赖性激酶 6(CDK6)-3'UTR,抑制了 CDK6 蛋白的表达。有趣的是,CDK6 的沉默抑制了牛前脂肪细胞的增殖和增殖相关基因的表达。因此,miR-33a 能抑制牛前脂肪细胞的增殖。CDK6 是 miR-33a 的靶基因,可能参与了 miR-33a 对牛前脂肪细胞增殖的影响。
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来源期刊
Adipocyte
Adipocyte Medicine-Histology
CiteScore
6.50
自引率
3.00%
发文量
46
审稿时长
32 weeks
期刊介绍: Adipocyte recognizes that the adipose tissue is the largest endocrine organ in the body, and explores the link between dysfunctional adipose tissue and the growing number of chronic diseases including diabetes, hypertension, cardiovascular disease and cancer. Historically, the primary function of the adipose tissue was limited to energy storage and thermoregulation. However, a plethora of research over the past 3 decades has recognized the dynamic role of the adipose tissue and its contribution to a variety of physiological processes including reproduction, angiogenesis, apoptosis, inflammation, blood pressure, coagulation, fibrinolysis, immunity and general metabolic homeostasis. The field of Adipose Tissue research has grown tremendously, and Adipocyte is the first international peer-reviewed journal of its kind providing a multi-disciplinary forum for research focusing exclusively on all aspects of adipose tissue physiology and pathophysiology. Adipocyte accepts high-profile submissions in basic, translational and clinical research.
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