Department of Infectious Disease, Qingdao Municipal Hospital, Qingdao University, 1 Jiaozhou Road, Qingdao, 266011, Shandong Province, China.
School of Medicine and Pharmacy, Ocean University of China, Qingdao, China.
Lipids Health Dis. 2022 Jun 15;21(1):54. doi: 10.1186/s12944-022-01662-6.
MicroRNAs (MiRNAs) are known to participate in preadipocyte differentiation, but the manner in which miR-146a-5p participates in this process remains unclear. This study was performed to examine the participation of miR-146a-5p in 3T3-L1 cell differentiation.
miR-146a-5p expression was upregulated and down-regulated to examine effects on 3T3-L1 cell differentiation. Bioinformatics analysis was performed to predict its target genes, and the signaling pathway it regulates was identified by qRT-PCR and Western blotting. The expression of miR-146a-5p in epididymal adipose tissue from obese mice and in an obese mouse adipose cell model was examined by qRT-PCR.
3T3-L1 cells differentiated into mature adipocytes successfully, as verified by increased areas of intracellular lipid droplets and elevated expression of mature adipocyte markers, and these cells had elevated miR-146a-5p expression. The intracellular lipid droplet and triglyceride contents and the expression of mature adipocyte markers were significantly increased in miR-146a-5p-overexpressing 3T3-L1 cells and markedly decreased in miR-146a-5p-inhibited 3T3-L1 cells. ErbB4 was a predicted target gene of miR-146a-5p. In miR-146a-5p-overexpressing 3T3-L1 cells, ErbB4 expression and ERK1/2 phosphorylation were decreased and the expression of PPAR-γ was increased; the opposite was observed in miR-146a-5p-inhibited 3T3-L1 cells. In addition, miR-146a-5p expression was significantly increased in the mouse epididymal adipose tissue and adipose cell model.
Upregulated miR-146a-5p expression was related to 3T3-L1 cell differentiation. MiR-146a-5p promoted 3T3-L1 cell differentiation by targeting ErbB4 and via the ERK1/2/PPAR-γ signaling pathway.
已知 microRNAs(miRNAs)参与前体脂肪细胞分化,但 miR-146a-5p 参与该过程的方式尚不清楚。本研究旨在研究 miR-146a-5p 在 3T3-L1 细胞分化中的作用。
上调和下调 miR-146a-5p 的表达,以观察对 3T3-L1 细胞分化的影响。通过生物信息学分析预测其靶基因,并通过 qRT-PCR 和 Western blot 鉴定其调节的信号通路。通过 qRT-PCR 检测肥胖小鼠附睾脂肪组织和肥胖小鼠脂肪细胞模型中 miR-146a-5p 的表达。
3T3-L1 细胞成功分化为成熟脂肪细胞,这可通过细胞内脂滴面积的增加和成熟脂肪细胞标志物的表达得到验证,并且这些细胞中 miR-146a-5p 的表达升高。在 miR-146a-5p 过表达的 3T3-L1 细胞中,细胞内脂滴和甘油三酯含量以及成熟脂肪细胞标志物的表达显著增加,而在 miR-146a-5p 抑制的 3T3-L1 细胞中则显著降低。ErbB4 是 miR-146a-5p 的一个预测靶基因。在 miR-146a-5p 过表达的 3T3-L1 细胞中,ErbB4 表达和 ERK1/2 磷酸化降低,而 PPAR-γ 表达增加;在 miR-146a-5p 抑制的 3T3-L1 细胞中则观察到相反的结果。此外,miR-146a-5p 的表达在小鼠附睾脂肪组织和脂肪细胞模型中显著增加。
上调的 miR-146a-5p 表达与 3T3-L1 细胞分化有关。miR-146a-5p 通过靶向 ErbB4 并通过 ERK1/2/PPAR-γ 信号通路促进 3T3-L1 细胞分化。