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细胞外基质衍生的生物物理线索介导间质液流动诱导的血管生成。

Extracellular Matrix-Derived Biophysical Cues Mediate Interstitial Flow-Induced Sprouting Angiogenesis.

机构信息

Department of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, Ohio 43210, United States.

Research Center for Applied Science, Academia Sinica, Taipei 115-29, Taiwan.

出版信息

ACS Appl Mater Interfaces. 2023 Mar 29;15(12):15047-15058. doi: 10.1021/acsami.2c15180. Epub 2023 Mar 14.

Abstract

Sprouting angiogenesis is orchestrated by an intricate balance of biochemical and mechanical cues in the local tissue microenvironment. Interstitial flow has been established as a potent regulator of angiogenesis. Similarly, extracellular matrix (ECM) physical properties, such as stiffness and microarchitecture, have also emerged as important mediators of angiogenesis. However, the interplay between interstitial flow and ECM physical properties in the initiation and control of angiogenesis is poorly understood. Using a three-dimensional (3D) microfluidic tissue analogue of angiogenic sprouting with defined interstitial flow superimposed over ECM with well-characterized physical properties, we found that the addition of hyaluronan (HA) to collagen-based matrices significantly enhances sprouting induced by interstitial flow compared to responses in collagen-only hydrogels. We confirmed that both the stiffness and matrix pore size of collagen-only hydrogels were increased by the addition of HA. Interestingly, interstitial flow-potentiated sprouting responses in collagen/HA matrices were not affected when functionally blocking the HA receptor CD44. In contrast, enzymatic depletion of HA in collagen/HA matrices with hyaluronidase (HAdase) resulted in decreased stiffness, pore size, and interstitial flow-mediated sprouting to the levels observed in collagen-only matrices. Taken together, these results suggest that HA enhances interstitial flow-mediated angiogenic sprouting through its alterations to collagen ECM stiffness and pore size.

摘要

血管生成是由局部组织微环境中的生化和力学线索的复杂平衡来调控的。间质流已被确定为血管生成的有效调节剂。同样,细胞外基质 (ECM) 的物理特性,如硬度和微观结构,也已成为血管生成的重要介质。然而,间质流和 ECM 物理特性在血管生成的启动和控制中的相互作用还知之甚少。我们使用具有定义的间质流的三维 (3D) 血管生成发芽的微流控组织模拟物,该间质流叠加在具有良好表征的物理特性的 ECM 上,发现与仅在胶原蛋白水凝胶中的反应相比,向胶原蛋白基质中添加透明质酸 (HA) 可显著增强间质流诱导的发芽。我们证实,仅添加 HA 就会增加胶原蛋白水凝胶的硬度和基质孔径。有趣的是,当功能性阻断 HA 受体 CD44 时,胶原蛋白/HA 基质中的间质流增强的发芽反应不受影响。相比之下,用透明质酸酶 (HAdase) 在胶原蛋白/HA 基质中耗尽 HA 会导致硬度、孔径和间质流介导的发芽降低至仅在胶原蛋白基质中观察到的水平。总之,这些结果表明,HA 通过改变胶原蛋白 ECM 的硬度和孔径来增强间质流介导的血管生成发芽。

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