Department of Pharmacology, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, Japan.
Am J Physiol Cell Physiol. 2013 Jun 1;304(11):C1091-7. doi: 10.1152/ajpcell.00343.2012. Epub 2013 Apr 10.
PDZRN3, a member of the PDZRN (or LNX) family of proteins, is essential for the differentiation of mesenchymal stem cells into myotubes, but it plays an inhibitory role in the differentiation of these cells into osteoblasts. Given that mesenchymal stem cells also differentiate into adipocytes, we examined the possible role of PDZRN3 in adipogenesis in mouse 3T3-L1 preadipocytes. The expression of PDZRN3 decreased at both the mRNA and protein levels during adipogenic differentiation. RNAi-mediated depletion of PDZRN3 enhanced the differentiation of 3T3-L1 cells into adipocytes as assessed on the basis of lipid accumulation. The upregulation of aP2 and CCAAT/enhancer-binding protein (C/EBP)-β during adipocyte differentiation was also enhanced in the PDZRN3-depleted cells, as was the induction of peroxisome proliferator-activated receptor-γ (PPARγ), an upstream regulator of aP2 and C/EBPα, at both the mRNA and protein levels. Among transcription factors that control the expression of PPARγ, we found that STAT5b, but not STAT5a, was upregulated in PDZRN3-depleted cells at both mRNA and protein levels. Tyrosine phosphorylation of STAT5b, but not that of STAT5a, was also enhanced at an early stage of differentiation by PDZRN3 depletion. In addition, the expression of C/EBPβ during the induction of differentiation was enhanced at the mRNA and protein levels in PDZRN3-depleted cells. Our results thus suggest that PDZRN3 negatively regulates adipogenesis in 3T3-L1 cells through downregulation of STAT5b and C/EBPβ and consequent suppression of PPARγ expression.
PDZRN3 是 PDZRN(或 LNX)蛋白家族的成员,对于间充质干细胞向肌管分化是必需的,但它在这些细胞向成骨细胞分化中起抑制作用。鉴于间充质干细胞也分化为脂肪细胞,我们研究了 PDZRN3 在小鼠 3T3-L1 前脂肪细胞成脂分化中的可能作用。在成脂分化过程中,PDZRN3 的 mRNA 和蛋白水平均降低。RNAi 介导的 PDZRN3 耗竭增强了 3T3-L1 细胞向脂肪细胞的分化,基于脂质积累进行评估。在 PDZRN3 耗竭细胞中,aP2 和 CCAAT/增强子结合蛋白(C/EBP)-β 的上调也增强,而过氧化物酶体增殖物激活受体-γ(PPARγ)的诱导,aP2 和 C/EBPα 的上游调节剂,在 mRNA 和蛋白水平上也是如此。在控制 PPARγ表达的转录因子中,我们发现 PDZRN3 耗竭细胞中 STAT5b 而不是 STAT5a 的 mRNA 和蛋白水平均上调。PDZRN3 耗竭还增强了 STAT5b 的酪氨酸磷酸化,但不增强 STAT5a 的酪氨酸磷酸化,在分化的早期阶段也是如此。此外,PDZRN3 耗竭细胞中 C/EBPβ 在诱导分化过程中的表达在 mRNA 和蛋白水平上均增强。因此,我们的结果表明 PDZRN3 通过下调 STAT5b 和 C/EBPβ 并抑制 PPARγ 表达,负调控 3T3-L1 细胞的成脂分化。