Analysis of Inward Vascular Remodeling Focusing on Endothelial–Perivascular Crosstalk in a Microfluidic Device

Pub Date : 2023-10-20 DOI:10.20965/jrm.2023.p1165
Ryosuke Murai, Masafumi Watanabe, Ryo Sudo
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Abstract

Vascular remodeling is a crucial process for the effective delivery of oxygen and nutrients to the entire body during vascular formation. However, detailed mechanisms underlying vascular remodeling are not yet fully understood owing to the absence of an appropriate experimental model. To address this, in this study, we utilized a microfluidic vascular model with perivascular cells to investigate the mechanism of vascular remodeling by culturing human umbilical vein endothelial cells (HUVECs) and mesenchymal stem cells (MSCs) in a microfluidic device. We compared two different cell culture conditions: culturing HUVECs and MSCs (1) separately in different channels and (2) in the same channel. In both conditions, microvascular networks covered with perivascular cells were formed. Interestingly, a significant inward vascular remodeling occurred over time when HUVECs and MSCs were cultured in different channels. This remodeling was mediated by direct endothelial–perivascular crosstalk through α 6 integrin. Furthermore, computational fluid analysis revealed that hypothetical shear stress on the luminal surface of microvessels was attenuated during inward vascular remodeling, suggesting that the remodeling might be an adaptive change. Our findings and the microfluidic model will be useful not only for further elucidation of mechanisms underlying physiological and pathological vascular remodeling but also for constructing functional vascularized tissues and organs by controlling vascular remodeling.
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以微流控装置内皮-血管周串扰为中心的血管内重构分析
血管重构是血管形成过程中氧气和营养物质向全身有效输送的关键过程。然而,由于缺乏适当的实验模型,血管重构的详细机制尚未完全了解。为了解决这一问题,本研究利用带血管周围细胞的微流控血管模型,通过在微流控装置中培养人脐静脉内皮细胞(HUVECs)和间充质干细胞(MSCs)来研究血管重塑的机制。我们比较了两种不同的细胞培养条件:HUVECs和MSCs(1)分别在不同的通道中培养,(2)在同一通道中培养。在这两种情况下,微血管网络都被血管周围细胞覆盖。有趣的是,当HUVECs和MSCs在不同的通道中培养时,随着时间的推移,显著的血管内重构发生了。这种重构是通过α 6整合素介导的内皮-血管周围直接串扰介导的。此外,计算流体分析显示,在向内血管重构过程中,微血管管腔表面的假设剪切应力减弱,表明重构可能是一种适应性变化。我们的发现和微流控模型不仅有助于进一步阐明生理和病理血管重构的机制,而且有助于通过控制血管重构来构建功能性的血管化组织和器官。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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