4.2 Article

MicroRNA-378 regulates adipogenic differentiation in bovine intramuscular preadipocytes by targeting CaMKK2

期刊

ADIPOCYTE
卷 10, 期 1, 页码 483-492

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/21623945.2021.1982526

关键词

Microrna-378; Camkk2; adipogenic differentiation; bovine; intramuscular preadipocytes

资金

  1. National Natural Science Foundation of China [31101696]
  2. Program of National Beef Cattle and Yak Industrial Technology System [CARS-37]
  3. Anhui Province Higher School Natural Science Key Program of China [KJ2018A0350]
  4. Anhui Province Science and Technology Major Special Project [202003a06020020, 201904f06020018]
  5. Fuyang Municipal Government [XDHX201736]
  6. Research Startup Fund of Fuyang Normal University
  7. Fuyang Normal University [XDHX201736]

向作者/读者索取更多资源

miR-378 plays a role in promoting adipogenic differentiation in bovine intramuscular preadipocytes by targeting CaMKK2 via the AMPK signalling pathway. The expression of miR-378 varies in different tissues and organs of cattle.
Intramuscular fat, as one of the most important palatability attribute of beef carcase, is the primary determinant of beef quality. The research of adipogenesis mechanism would provide new insight into intramuscular fatty deposition. Here, the role of microRNA-378 was investigated during bovine adipogenic differentiation. It was revealed that miR-378 expression exists variably in bovine major tissue and organs by RT-qPCR. It was predicted that miR-378 targets CaMKK2, as an AMPK alpha kinase, by DIANA Tools. For better research, primary preadipocytes with stable transfection for up-/down-regulated expression of miR-378 were constructed by lentiviral vectors with GFP gene. The analyses of qPCR showed that PPAR gamma and adiponectin mRNA levels increased, but C/EBP beta, pref-1 and CaMKK2 mRNA levels decreased during adipogenic differentiation. When miR-378 was overexpressed, preadipocytes proliferation became slower, there are more cellular lipid droplets, and PPAR gamma and C/EBP beta mRNA levels were higher, but pref-1, adiponectin and CaMKK2 were lower than control groups. Luciferase assay and western blot analysis validated that miR-378 binds the nucleotide sites of the 3 '- untranslated region of CaMKK2, which inhibits the mRNA and protein expression of CaMKK2. These findings suggest that miR-378 promotes adipogenic differentiation in bovine intramuscular preadipocytes by targeting CaMKK2 via AMPK signalling pathway.

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