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Plant miR167e-5p promotes 3T3-L1 adipocyte adipogenesis by targeting β-catenin.

Authors :
Chen, Ting
Ma, Fei
Peng, Yongjia
Sun, Ruiping
Xi, Qianyun
Sun, Jiajie
Zhang, Jin
Zhang, Yongliang
Li, Meng
Source :
In Vitro Cellular & Developmental Biology Animal; Jun2022, Vol. 58 Issue 6, p471-479, 9p
Publication Year :
2022

Abstract

Adipogenesis is important in the development of fat deposition. Evidence showed that plant microRNAs (miRNAs) could be absorbed by the digestive tract and exert regulatory effects on animals' physiological processes. However, the regulation of plant miRNA on host lipogenesis remains unknown. This study explored the potential function of plant miRNA, miR167e-5p, in adipogenesis in vitro. The presentation of plant miR167e-5p improved lipid accumulation in 3T3-L1 cells. Bioinformatics prediction and luciferase reporter assay indicated that miR167e-5p targeted β-catenin. MiR167e-5p could not only negatively affect the expression of β-catenin but also showed a positive effect on several fat synthesis–related genes, peroxisome proliferator–activated receptor gamma (Pparγ), CCAAT/enhancer-binding protein α (Cebpα), fatty acid-binding protein 4 (Ap2), lipolysis genes, adipose triglyceride lipase (Atgl), and hormone-sensitive lipase (Hsl) messenger RNA levels. Meanwhile, lipid accumulation and the expression of the β-catenin and other five fat synthesis–related genes were recovered to their original pattern by adding the miR167e-5p inhibitor in 3T3-L1 cells. The immunoblot confirmed the same expression pattern in protein levels in β-catenin, PPAR-γ, FAS, and HSL. This research demonstrates that plant miR167e-5p can potentially affect adipogenesis through the regulation of β-catenin, suggesting that plant miRNAs could be a new class of bioactive ingredients in adipogenesis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10712690
Volume :
58
Issue :
6
Database :
Complementary Index
Journal :
In Vitro Cellular & Developmental Biology Animal
Publication Type :
Academic Journal
Accession number :
158111646
Full Text :
https://doi.org/10.1007/s11626-022-00702-w