Walther Brandon K, Rajeeva Pandian Navaneeth Krishna, Gold Karli A, Kiliç Ecem S, Sama Vineeth, Gu Jianhua, Gaharwar Akhilesh K, Guiseppi-Elie Anthony, Cooke John P, Jain Abhishek
Department of Biomedical Engineering, Texas A&M University, College Station, Texas 77843, USA.
Department of Biomedical Engineering, Clemson University, Clemson, South Carolina 29634, USA.
Lab Chip. 2021 May 4;21(9):1738-1751. doi: 10.1039/d0lc01283a.
Endothelial mechanobiology is a key consideration in the progression of vascular dysfunction, including atherosclerosis. However mechanistic connections between the clinically associated physical stimuli, vessel stiffness and shear stress, and how they interact to modulate plaque progression remain incompletely characterized. Vessel-chip systems are excellent candidates for modeling vascular mechanobiology as they may be engineered from the ground up, guided by the mechanical parameters present in human arteries and veins, to recapitulate key features of the vasculature. Here, we report extensive validation of a vessel-chip model of endothelial yes-associated protein (YAP) mechanobiology, a protein sensitive to both matrix stiffness and shearing forces and, importantly, implicated in atherosclerotic progression. Our model captures the established endothelial mechanoresponse, with endothelial alignment, elongation, reduction of adhesion molecules, and YAP cytoplasmic retention under high laminar shear. Conversely, we observed disturbed morphology, inflammation, and nuclear partitioning under low, high, and high oscillatory shear. Examining targets of YAP transcriptional co-activation, connective tissue growth factor (CTGF) is strongly downregulated by high laminar shear, whereas it is strongly upregulated by low shear or oscillatory flow. Ankyrin repeat domain 1 (ANKRD1) is only upregulated by high oscillatory shear. Verteporfin inhibition of YAP reduced the expression of CTGF but did not affect ANKRD1. Lastly, substrate stiffness modulated the endothelial shear mechanoresponse. Under high shear, softer substrates showed the lowest nuclear localization of YAP whereas stiffer substrates increased nuclear localization. Low shear strongly increased nuclear localization of YAP across stiffnesses. Together, we have validated a model of endothelial mechanobiology and describe a clinically relevant biological connection between matrix stiffness, shear stress, and endothelial activation via YAP mechanobiology.
内皮细胞力学生物学是血管功能障碍(包括动脉粥样硬化)进展中的一个关键因素。然而,临床相关的物理刺激、血管硬度和剪切应力之间的机制联系,以及它们如何相互作用来调节斑块进展,仍未完全明确。血管芯片系统是模拟血管力学生物学的理想选择,因为它们可以根据人体动脉和静脉中存在的机械参数从头开始设计,以重现脉管系统的关键特征。在此,我们报告了一种内皮细胞Yes相关蛋白(YAP)力学生物学血管芯片模型的广泛验证,YAP是一种对基质硬度和剪切力均敏感的蛋白,并且重要的是,与动脉粥样硬化进展有关。我们的模型捕捉到了已确立的内皮机械反应,即在高切应力下内皮细胞排列、伸长、黏附分子减少以及YAP保留在细胞质中。相反,在低、高和高振荡切应力下,我们观察到细胞形态紊乱、炎症和核定位变化。研究YAP转录共激活的靶点发现,高切应力强烈下调结缔组织生长因子(CTGF),而低切应力或振荡流则强烈上调CTGF。锚蛋白重复结构域1(ANKRD1)仅在高振荡切应力下上调。维替泊芬抑制YAP可降低CTGF的表达,但不影响ANKRD1。最后,底物硬度调节内皮细胞的剪切机械反应。在高切应力下,较软的底物显示YAP的核定位最低,而较硬的底物则增加核定位。低切应力在不同硬度条件下均强烈增加YAP的核定位。总之,我们验证了一种内皮细胞力学生物学模型,并描述了基质硬度、剪切应力和通过YAP力学生物学介导的内皮细胞激活之间的临床相关生物学联系。