Chiu Jeng-Jiann, Chen Li-Jing, Lee Pei-Ling, Lee Chih-I, Lo Leu-Wei, Usami Shunichi, Chien Shu
Division of Medical Engineering Research, National Health Research Institutes, Taipei, Taiwan, Republic of China.
Blood. 2003 Apr 1;101(7):2667-74. doi: 10.1182/blood-2002-08-2560. Epub 2002 Dec 5.
Vascular endothelial cells (ECs), which exist in close proximity to vascular smooth muscle cells (SMCs), are constantly subjected to blood flow-induced shear stress. Although the effect of shear stress on endothelial biology has been extensively studied, the influence of SMCs on endothelial response to shear stress remains largely unexplored. We examined the potential role of SMCs in regulating the shear stress-induced gene expression in ECs, using a parallel-plate coculture flow system in which these 2 types of cells were separated by a porous membrane. In this coculture system, SMCs tended to orient perpendicularly to the flow direction, whereas the ECs were elongated and aligned with the flow direction. Under static conditions, coculture with SMCs induced EC gene expression of intercellular adhesion molecule-1 (ICAM-1), vascular adhesion molecule-1 (VCAM-1), and E-selectin, while attenuating EC gene expression of endothelial nitric oxide synthase (eNOS). Shear stress significantly inhibited SMC-induced adhesion molecule gene expression. These EC responses under static and shear conditions were not observed in the absence of close communication between ECs and SMCs, and they were also not observed when ECs were cocultured with fibroblasts instead of SMCs. Our findings indicate that under static conditions, coculture with SMCs induces ICAM-1, VCAM-1, and E-selectin gene expression in ECs. These coculture effects are inhibited by shear stress and require specific interaction between ECs and SMCs in close contact.
血管内皮细胞(ECs)与血管平滑肌细胞(SMCs)紧密相邻,不断受到血流诱导的剪切应力作用。尽管剪切应力对内皮生物学的影响已得到广泛研究,但SMCs对内皮细胞对剪切应力反应的影响在很大程度上仍未被探索。我们使用平行板共培养流动系统,研究了SMCs在调节ECs中剪切应力诱导的基因表达方面的潜在作用,在该系统中这两种类型的细胞被多孔膜分隔。在这个共培养系统中,SMCs倾向于垂直于流动方向排列,而ECs则伸长并与流动方向对齐。在静态条件下,与SMCs共培养会诱导细胞间黏附分子-1(ICAM-1)、血管黏附分子-1(VCAM-1)和E-选择素的EC基因表达,同时减弱内皮型一氧化氮合酶(eNOS)的EC基因表达。剪切应力显著抑制了SMCs诱导的黏附分子基因表达。在ECs和SMCs之间缺乏密切通讯的情况下,未观察到静态和剪切条件下的这些EC反应,并且当ECs与成纤维细胞而非SMCs共培养时也未观察到这些反应。我们的研究结果表明,在静态条件下,与SMCs共培养会诱导ECs中ICAM-1、VCAM-1和E-选择素基因表达。这些共培养效应受到剪切应力的抑制,并且需要紧密接触的ECs和SMCs之间的特定相互作用。