Huang Zenan, Cheng Xiaofei, Zhao Jie, Liu Zhongjun, Wang Jingcheng, Feng Xinmin, Zhang Liang
Department of Orthopaedics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011,China.
Department of Orthopaedics, Peking University Third Hospital, Beijing 100191,China.
Iran J Basic Med Sci. 2019 Dec;22(12):1468-1475. doi: 10.22038/IJBMS.2019.14068.
This research is to study the influences of different concentrations of simvastatin on the biological activities of nucleus pulposus-derived mesenchymal stem cells (NPMSC).
NPMSC were cultured with different concentrations of simvastatin (0, 0.01, 0.1, and 1 μM) and assessed to determine the possible effects of simvastatin. The cell proliferation was assessed with CCK-8 assay. The flowcytometry and multilineage differentiation were also performed to identify the stem characterization of the cells. The mRNA expressions of aggrecan, collagen type II, glucose transporter 1 (GLUT-1), vascular endothelial growth factor (VEGF) and hypoxia-inducible factor-1α (HIF-1α) were determined by qRT-PCR.
The results demonstrated that the cells isolated from nucleus pulposus of healthy Sprague-Dawley (SD) rat met the criteria of MSC. NPMSC could form sunflower-like colonies and strongly expressed stem cell-related genes. In addition, NPMSC showed strong ability of chondrogenic, adipogenic and osteogenic differentiation. Simvastatin at certain range concentrations (0.01 μM-0.1 μM)) significantly promoted colony-forming rate and cell proliferation, and inhibited cell apoptosis. Simvastatin could promote expressions of aggrecan, collagen type II, HIF-1α, VEGF and GLUT-1, while 0.1 μmol/l concentration reached the maximum effect. Our study further demonstrated that HIF-1α-intermediated signaling pathway might participate in regulating the biological activities of NPMSC.
Proper concentration of simvastatin can promote the biological behavior of NPMSC, and HIF-1α-intermediated signaling pathway might participate in the mechanism.
本研究旨在探讨不同浓度辛伐他汀对髓核来源间充质干细胞(NPMSC)生物学活性的影响。
将NPMSC与不同浓度的辛伐他汀(0、0.01、0.1和1 μM)共同培养,评估辛伐他汀可能产生的作用。采用CCK-8法检测细胞增殖情况。还进行了流式细胞术和多向分化实验以鉴定细胞的干细胞特性。通过qRT-PCR检测聚集蛋白聚糖、Ⅱ型胶原、葡萄糖转运蛋白1(GLUT-1)、血管内皮生长因子(VEGF)和缺氧诱导因子-1α(HIF-1α)的mRNA表达。
结果表明,从健康Sprague-Dawley(SD)大鼠髓核中分离出的细胞符合间充质干细胞的标准。NPMSC可形成向日葵样集落,并强烈表达干细胞相关基因。此外,NPMSC表现出较强的成软骨、成脂和成骨分化能力。一定浓度范围(0.01 μM - 0.1 μM)的辛伐他汀显著提高集落形成率和细胞增殖能力,并抑制细胞凋亡。辛伐他汀可促进聚集蛋白聚糖、Ⅱ型胶原、HIF-1α、VEGF和GLUT-1的表达,其中0.1 μmol/l浓度时作用效果最佳。我们的研究进一步表明,HIF-1α介导的信号通路可能参与调节NPMSC的生物学活性。
适当浓度的辛伐他汀可促进NPMSC的生物学行为,且HIF-1α介导的信号通路可能参与其中。