Aji Kaisaier, Maimaijiang Munila, Aimaiti Abudusaimi, Rexiati Mulati, Azhati Baihetiya, Tusong Hamulati, Cui Lei
Department of Urology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang 830054, China.
Prevention and Health Care Department, The Second Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang 830063, China.
Stem Cells Int. 2016;2016:1267480. doi: 10.1155/2016/1267480. Epub 2016 Jul 14.
The multifunctional Ca(2+)/calmodulin-dependent protein kinase II (CaMKII) is known to participate in maintenance and switches of smooth muscle cell (SMC) phenotypes. However, which isoform of CaMKII is involved in differentiation of adult mesenchymal stem cells into contractile SMCs remains unclear. In the present study, we detected γ isoform of CaMKII in differentiation of human adipose derived stem cells (hASCs) into SMCs that resulted from treatment with TGF-β1 and BMP4 in combination for 7 days. The results showed that CaMKIIγ increased gradually during differentiation of hASCs as determined by real-time PCR and western blot analysis. The siRNA-mediated knockdown of CaMKIIγ decreased the protein levels and transcriptional levels of smooth muscle contractile markers (a-SMA, SM22a, calponin, and SM-MHC), while CaMKIIγ overexpression increases the transcriptional and protein levels of smooth muscle contractile markers. These results suggested that γ isoform of CaMKII plays a significant role in smooth muscle differentiation of hASCs.
多功能的钙/钙调蛋白依赖性蛋白激酶II(CaMKII)已知参与平滑肌细胞(SMC)表型的维持和转换。然而,CaMKII的哪种亚型参与成年间充质干细胞向收缩性SMC的分化仍不清楚。在本研究中,我们在人脂肪来源干细胞(hASC)分化为SMC的过程中检测到CaMKII的γ亚型,该分化过程是由转化生长因子-β1(TGF-β1)和骨形态发生蛋白4(BMP4)联合处理7天导致的。结果显示,通过实时定量聚合酶链反应(PCR)和蛋白质免疫印迹分析确定,在hASC分化过程中CaMKIIγ逐渐增加。小干扰RNA(siRNA)介导的CaMKIIγ敲低降低了平滑肌收缩标志物(α-平滑肌肌动蛋白(α-SMA)、平滑肌22α蛋白(SM22α)、钙调蛋白和平滑肌肌球蛋白重链(SM-MHC))的蛋白质水平和转录水平,而CaMKIIγ过表达则增加了平滑肌收缩标志物的转录和蛋白质水平。这些结果表明,CaMKII的γ亚型在hASC的平滑肌分化中起重要作用。