Department of Cardiology, The First Affiliated Hospital of China Medical University, Shenyang, PR China.
Int J Mol Med. 2011 Nov;28(5):777-83. doi: 10.3892/ijmm.2011.744. Epub 2011 Jul 8.
Excessive proliferation of vascular smooth muscle cells (VSMCs) is an important reason for the formation and development of many vascular remodeling diseases. In pathological conditions, necrosis of VSMCs may result in the release of inflammatory cytokines, which can lead to stimulation of other normal smooth muscle cells, and promote the proliferation of VSMCs. The purpose of this study was to investigate the effect of oxygen- and glucose-deprived (OGD) conditioned medium on VSMC cell proliferation and invasion. Following culture of VSMCs in OGD-conditioned medium, the cell cycle distributions were remarkably altered. The number of cells in the G0/G1 phase decreased, while the number of cells in G2/M and S phase increased. The expression of cell cycle proteins D1 (Cyclin D1) in VSMCs increased correspondingly. These results suggested that after being cultured in OGD medium, VSMCs can pass through the G0/G1 phase by up-regulation of Cyclin D1 expression, and promote cell proliferation. In addition, we found that the expression of matrix metalloproteinase (MMP)-2 and MMP-9 was increased in OGD medium cultured VSMCs. Using a Transwell invasion assay, we showed that the OGD medium enhanced VSMC cell invasion. These results suggest that MMP-2 and MMP-9 degraded the basement membrane and promoted VSMC invasion. Taken together, our data demonstrate that OGD-conditioned medium can promote VSMC proliferation and invasion by up-regulating Cyclin D1 and MMP-2 and MMP-9 expression, which may contribute to the formation and development of vascular remodeling diseases.
血管平滑肌细胞(VSMCs)的过度增殖是许多血管重构疾病形成和发展的重要原因。在病理条件下,VSMCs 的坏死可能导致炎症细胞因子的释放,这可能导致对其他正常平滑肌细胞的刺激,并促进 VSMCs 的增殖。本研究旨在探讨缺氧/低糖(OGD)条件培养基对 VSMC 细胞增殖和侵袭的影响。在 OGD 条件培养基中培养 VSMCs 后,细胞周期分布发生明显改变。G0/G1 期细胞数量减少,而 G2/M 和 S 期细胞数量增加。VSMCs 中细胞周期蛋白 D1(Cyclin D1)的表达相应增加。这些结果表明,在 OGD 培养基中培养后,VSMCs 可以通过上调 Cyclin D1 表达来通过 G0/G1 期,促进细胞增殖。此外,我们发现 OGD 培养基培养的 VSMCs 中基质金属蛋白酶(MMP)-2 和 MMP-9 的表达增加。通过 Transwell 侵袭实验,我们表明 OGD 培养基增强了 VSMC 细胞的侵袭。这些结果表明 MMP-2 和 MMP-9 降解了基底膜并促进了 VSMC 侵袭。总之,我们的数据表明,OGD 条件培养基通过上调 Cyclin D1 和 MMP-2 和 MMP-9 的表达来促进 VSMC 的增殖和侵袭,这可能有助于血管重构疾病的形成和发展。