Matrix stiffening in the formation of blood vessels

Danielle J. LaValley, C. Reinhart-King
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引用次数: 30

Abstract

Angiogenesis, the process where new blood vessels form from existing vasculature, is essential for the successful integration of most tissue-engineered constructs and is dysregulated in many diseases, including cancer. To be functional, the newly formed vasculature must have similar structure and integrity as existing blood vessels, both of which are dependent upon mechanical and chemical cues from the surrounding extracellular matrix (ECM). ECM stiffness has emerged as a critical extracellular parameter that can modulate capillary network formation and barrier integrity. Moreover, matrix stiffness can alter how endothelial cells respond to soluble, angiogenic factors released by stromal cells, such as vascular endothelial growth factor (VEGF). In this review, we will discuss how matrix stiffness can affect the formation and structure of angiogenic vessels, and we will highlight the role of this work in the development of therapeutics to treat angiogenesis in cancer. Knowledge of the governing parameters for vessel formation is critical to the intelligent design of materials made to foster blood vessel growth for tissue-engineering applications and pharmaceuticals designed to intervene with newly formed vasculature in diseased tissue.
血管形成过程中基质硬化
血管生成是现有血管系统形成新血管的过程,对于大多数组织工程结构的成功整合至关重要,并且在包括癌症在内的许多疾病中失调。为了发挥功能,新形成的血管系统必须具有与现有血管相似的结构和完整性,这两者都依赖于来自周围细胞外基质(ECM)的机械和化学线索。ECM刚度已经成为一个关键的细胞外参数,可以调节毛细血管网络的形成和屏障的完整性。此外,基质硬度可以改变内皮细胞对基质细胞释放的可溶性血管生成因子(如血管内皮生长因子(VEGF))的反应。在这篇综述中,我们将讨论基质刚度如何影响血管生成血管的形成和结构,并强调这项工作在治疗癌症血管生成的治疗方法开发中的作用。血管形成的控制参数的知识对于用于组织工程应用的促进血管生长的材料的智能设计和用于干预病变组织中新形成的血管的药物设计至关重要。
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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