4.7 Article

miR-429 Inhibits Differentiation and Promotes Proliferation in Porcine Preadipocytes

期刊

出版社

MDPI AG
DOI: 10.3390/ijms17122047

关键词

miR-429; proliferation; differentiation; porcine subcutaneous preadipocytes; porcine intramuscular preadipocytes; KLF9; p27

资金

  1. National Science and Technology Major Project of China [2016ZX08006003]
  2. National Basic Research Program of China [2015CB943102]
  3. Major Projects for Genetically Modified Organisms Breeding [2014ZX08009-047B]

向作者/读者索取更多资源

MicroRNAs (miRNAs) are crucial regulatory molecules for adipogenesis. They contribute to the controlling of proliferation and differentiation of preadipocytes. Previous studies revealed an important role of miR-429 in cell invasion, migration, and apoptosis. Our previous work has shown that the expression of miR-429 in subcutaneous fat can be observed in newly born (3-day-old) Rongchang piglets rather than their adult counterparts (180-day-old). This expression pattern suggests that miR-429 might be functionally related to postnatal adipogenesis. However, we currently lack a mechanistic understanding of miR-429 within the context of preadipocyte differentiation. In this study, we investigated the function of miR-429 in porcine subcutaneous and intramuscular preadipocyte proliferation and differentiation. In our porcine preadipocyte differentiation model, miR-429 expression decreased remarkably upon adipogenic induction. Overexpression of miR-429 notably down-regulated the expression of adipogenic marker genes: PPAR gamma, aP2, FAS and impaired the triglyceride accumulation, while the expression of lipolytic gene ATGL was not affected. In addition, we observed that miR-429 significantly promoted the proliferation of porcine preadipocytes. We also found that miR-429 could directly bind to the 3'-UTRs of KLF9 and p27, which have been well documented to promote preadipocyte differentiation and repress cell cycle progression. Taken together, our data support a novel role of miR-429 in regulating porcine preadipocyte differentiation and proliferation, and KLF9 and p27 are potent targets of miR-429 during these processes.

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