College of Life Sciences, Shandong Agricultural University, Tai'an 271018, China.
College of Life Sciences, Shandong Agricultural University, Tai'an 271018, China.
Mol Cell Endocrinol. 2014 Feb 15;382(2):814-24. doi: 10.1016/j.mce.2013.11.006. Epub 2013 Nov 15.
The interferon-inducible protein 202 (p202) has emerged as a key regulator of cell proliferation and differentiation. To explore the role of p202 in adipocyte differentiation, p202 mRNA and protein levels in differentiating mouse adipose-derived stem cells (mASCs) were examined, and were found to continuously increase during mASC adipogenesis. The nuclear and cytoplasmic distribution of p202 in the differentiation process was also determined. In addition, suppression and overexpression of p202 impaired and enhanced the differentiation process, respectively. Further, results of co-immunoprecipitation and co-immunofluorescence showed the interaction and intracellular co-localization of p202 with C/EBPβ, C/EBPα, and PPARγ at intermediate and/or late differentiation stages. Knockdown of p202 interfered with the elevated expression of C/EBPβ, C/EBPα, and PPARγ. In conclusion, the temporal and spatial profiles of p202 and the observed manner in which p202 affected the expression of these transcription factors provided evidence that p202 plays a role during mASC adipogenesis.
干扰素诱导蛋白 202(p202)已成为细胞增殖和分化的关键调节因子。为了探索 p202 在脂肪细胞分化中的作用,检测了分化中的小鼠脂肪源性干细胞(mASCs)中 p202 mRNA 和蛋白水平,发现其在 mASC 脂肪生成过程中持续增加。还确定了 p202 在分化过程中的核质分布。此外,p202 的抑制和过表达分别削弱和增强了分化过程。此外,免疫共沉淀和免疫荧光共定位的结果表明,p202 与 C/EBPβ、C/EBPα 和 PPARγ 在中期和/或晚期分化阶段相互作用并在细胞内共定位。p202 的敲低干扰了 C/EBPβ、C/EBPα 和 PPARγ 的上调表达。总之,p202 的时空调控模式及其对这些转录因子表达的影响方式为 p202 在 mASC 脂肪生成过程中发挥作用提供了证据。