Li Ning, Wang Chengzhi, Sun Shujin, Zhang Chen, Lü Dongyuan, Chen Qin, Long Mian
Key Laboratory of Microgravity - National Microgravity Laboratory, Center of Biomechanics and Bioengineering, Beijing Key Laboratory of Engineered Construction and Mechanobiology, Institute of Mechanics, Chinese Academy of Sciences, Beijing, China.
School of Engineering Sciences, University of Chinese Academy of Sciences, Beijing, China.
Front Physiol. 2018 Jul 31;9:1025. doi: 10.3389/fphys.2018.01025. eCollection 2018.
Endothelial cells (ECs) are mechanosensitive cells undergoing morphological and functional changes in space. Ground-based study has provided a body of evidences about how ECs can respond to the effect of simulated microgravity, however, these results need to be confirmed by spaceflight experiments in real microgravity. In this work, we cultured EA.hy926 ECs on board the SJ-10 Recoverable Scientific Satellite for 3 and 10 days, and analyzed the effects of space microgravity on the ECs. Space microgravity suppressed the glucose metabolism, modulated the expression of cellular adhesive molecules such as ICAM-1, VCAM-1, and CD44, and depressed the pro-angiogenesis and pro-inflammation cytokine secretion. Meanwhile, it also induced the depolymerization of actin filaments and microtubules, promoted the vimentin accumulation, restrained the collagen I and fibronectin deposition, regulated the mechanotransduction through focal adhesion kinase and Rho GTPases, and enhanced the exosome-mediated mRNA transfer. Unlike the effect of simulated microgravity, neither three-dimensional growth nor enhanced nitric oxide production was observed in our experimental settings. This work furthers the understandings in the effects and mechanisms of space microgravity on ECs, and provides useful information for future spaceflight experimental design.
内皮细胞(ECs)是对机械敏感的细胞,在空间中会发生形态和功能变化。地面研究已经提供了大量关于ECs如何响应模拟微重力影响的证据,然而,这些结果需要通过实际微重力环境下的太空飞行实验来证实。在这项工作中,我们将EA.hy926内皮细胞搭载于实践十号返回式科学卫星上培养3天和10天,并分析太空微重力对这些细胞的影响。太空微重力抑制了葡萄糖代谢,调节了细胞黏附分子如ICAM-1、VCAM-1和CD44的表达,并抑制了促血管生成和促炎细胞因子的分泌。同时,它还诱导了肌动蛋白丝和微管的解聚,促进了波形蛋白的积累,抑制了I型胶原蛋白和纤连蛋白的沉积,通过粘着斑激酶和Rho GTPases调节机械转导,并增强了外泌体介导的mRNA转移。与模拟微重力的影响不同,在我们的实验条件下未观察到三维生长或一氧化氮产生增加。这项工作进一步加深了对太空微重力对内皮细胞影响及其机制的理解,并为未来的太空飞行实验设计提供了有用信息。