Brenner Shirley, Bercovich Zippi, Feiler Yulia, Keshet Rom, Kahana Chaim
Department of Molecular Genetics, The Weizmann Institute of Science, Rehovot 7610001, Israel.
Department of Molecular Genetics, The Weizmann Institute of Science, Rehovot 7610001, Israel.
J Biol Chem. 2015 Nov 6;290(45):27384-27392. doi: 10.1074/jbc.M115.686980. Epub 2015 Sep 22.
Adipogenesis is a complex process, accompanied by a chain of interdependent events. Disruption of key events in this cascade may interfere with the correct formation of adipose tissue. Polyamines were demonstrated necessary for adipogenesis; however, the underlying mechanism by which they act has not been established. Here, we examined the effect of polyamine depletion on the differentiation of 3T3-L1 preadipocytes. Our results demonstrate that polyamines are required early in the adipogenic process. Polyamine depletion inhibited the second division of the mitotic clonal expansion (MCE), and inhibited the expression of PPARγ and C/EBPα, the master regulators of adipogenesis. However, it did not affect the expression of their transcriptional activator, C/EBPβ. Additionally, polyamine depletion resulted in elevation of mRNA and protein levels of the stress-induced C/EBP homologous protein (CHOP), whose dominant negative function is known to inhibit C/EBPβ DNA binding activity. Conditional knockdown of CHOP in polyamine-depleted preadipocytes restored PPARγ and C/EBPα expression, but failed to recover MCE and differentiation. Thus, our results suggest that the need for MCE in the adipogenic process is independent from the requirement for PPARγ and C/EBPα expression. We conclude that de novo synthesis of polyamines during adipogenesis is required for down-regulation of CHOP to allow C/EBPβ activation, and for promoting MCE.
脂肪生成是一个复杂的过程,伴随着一系列相互依存的事件。这一连串事件中关键环节的破坏可能会干扰脂肪组织的正常形成。多胺已被证明是脂肪生成所必需的;然而,其作用的潜在机制尚未明确。在此,我们研究了多胺耗竭对3T3-L1前脂肪细胞分化的影响。我们的结果表明,多胺在脂肪生成过程的早期是必需的。多胺耗竭抑制了有丝分裂克隆扩增(MCE)的第二次分裂,并抑制了脂肪生成的主要调节因子PPARγ和C/EBPα的表达。然而,它并不影响其转录激活因子C/EBPβ的表达。此外,多胺耗竭导致应激诱导的C/EBP同源蛋白(CHOP)的mRNA和蛋白质水平升高,已知其显性负功能可抑制C/EBPβ的DNA结合活性。在多胺耗竭的前脂肪细胞中条件性敲低CHOP可恢复PPARγ和C/EBPα的表达,但未能恢复MCE和分化。因此,我们的结果表明,脂肪生成过程中对MCE的需求独立于对PPARγ和C/EBPα表达的需求。我们得出结论,脂肪生成过程中多胺的从头合成对于下调CHOP以激活C/EBPβ以及促进MCE是必需的。