Han Xiaobo, Sakamoto Naoya, Tomita Noriko, Meng Hui, Sato Masaaki, Ohta Makoto
Graduate School of Biomedical Engineering, Tohoku University, 2-1-1, Katahira, Aoba-ku, Sendai, Japan.
Department of Intelligent Mechanical Systems, Tokyo Metropolitan University, Hachioji, Japan.
Cytotechnology. 2019 Apr;71(2):489-496. doi: 10.1007/s10616-018-0268-7. Epub 2019 Feb 1.
Recently, our group has contrasted an endothelial cell-smooth muscle cell (EC-SMC) co-culture model with 3D-cultured SMCs and found that SMCs could respond to high shear stress (SS), which has not been explored before. SMCs were not directly exposed to the flow but were under an EC monolayer; therefore, it is necessary to explore the influence of EC on SMC behaviors under high SS for understanding the mechanism of SMC response to various magnitudes of SS. In the present study, TGF-β1 expression in ECs in an EC-SMC co-culture model was suppressed by an siRNA transfection method. Next, phenotypic changes were observed and MMP-2 and -9 productions were measured in SMCs in the co-culture model after 72-h flow exposure to different SS levels. We confirmed that TGF-β1 expression in ECs could influence SMC phenotypic change under SS conditions and that TGF-β1 expression in ECs could also change MMP-2 production but not MMP-9 production in SMCs under SS conditions in the co-culture model. These results could be useful for understanding the mechanisms of SMC response to SS, particularly for understanding signal transduction emanating from ECs.
最近,我们团队将内皮细胞-平滑肌细胞(EC-SMC)共培养模型与三维培养的平滑肌细胞进行了对比,发现平滑肌细胞能够对高剪切应力(SS)作出反应,这一点此前尚未被研究过。平滑肌细胞并未直接暴露于流体中,而是处于内皮细胞单层之下;因此,有必要探究内皮细胞在高剪切应力条件下对平滑肌细胞行为的影响,以了解平滑肌细胞对不同强度剪切应力作出反应的机制。在本研究中,通过小干扰RNA转染方法抑制了EC-SMC共培养模型中内皮细胞的转化生长因子-β1(TGF-β1)表达。接下来,在共培养模型中的平滑肌细胞经72小时不同剪切应力水平的流体暴露后,观察其表型变化并检测基质金属蛋白酶-2(MMP-2)和基质金属蛋白酶-9(MMP-9)的产生情况。我们证实,在内皮细胞中TGF-β1的表达能够在剪切应力条件下影响平滑肌细胞的表型变化,并且在内皮细胞中TGF-β1的表达还能够改变共培养模型中平滑肌细胞在剪切应力条件下MMP-2的产生,但不会改变MMP-9的产生。这些结果可能有助于理解平滑肌细胞对剪切应力作出反应的机制,特别是有助于理解源自内皮细胞的信号转导。