Mongiat Maurizio, Andreuzzi Eva, Tarticchio Giulia, Paulitti Alice
Experimental Oncology Division 2, Department of Translational Research, CRO-IRCCS, Aviano 33081, Italy.
Int J Mol Sci. 2016 Nov 1;17(11):1822. doi: 10.3390/ijms17111822.
The extracellular matrix (ECM) is a complex network of proteins, glycoproteins, proteoglycans, and polysaccharides. Through multiple interactions with each other and the cell surface receptors, not only the ECM determines the physical and mechanical properties of the tissues, but also profoundly influences cell behavior and many physiological and pathological processes. One of the functions that have been extensively explored is its impingement on angiogenesis. The strong impact of the ECM in this context is both direct and indirect by virtue of its ability to interact and/or store several growth factors and cytokines. The aim of this review is to provide some examples of the complex molecular mechanisms that are elicited by these molecules in promoting or weakening the angiogenic processes. The scenario is intricate, since matrix remodeling often generates fragments displaying opposite effects compared to those exerted by the whole molecules. Thus, the balance will tilt towards angiogenesis or angiostasis depending on the relative expression of pro- or anti-angiogenetic molecules/fragments composing the matrix of a given tissue. One of the vital aspects of this field of research is that, for its endogenous nature, the ECM can be viewed as a reservoir to draw from for the development of new more efficacious therapies to treat angiogenesis-dependent pathologies.
细胞外基质(ECM)是由蛋白质、糖蛋白、蛋白聚糖和多糖组成的复杂网络。通过彼此之间以及与细胞表面受体的多种相互作用,ECM不仅决定了组织的物理和机械特性,还深刻影响细胞行为以及许多生理和病理过程。其中一个已被广泛研究的功能是其对血管生成的影响。在这种情况下,ECM的强烈影响是直接的,也是间接的,因为它能够相互作用和/或储存多种生长因子和细胞因子。本综述的目的是提供一些由这些分子引发的促进或减弱血管生成过程的复杂分子机制的例子。情况很复杂,因为基质重塑常常产生与整个分子所发挥的作用相反的片段。因此,取决于构成给定组织基质的促血管生成或抗血管生成分子/片段的相对表达,平衡将倾向于血管生成或血管生成抑制。该研究领域的一个重要方面是,由于其内在性质,ECM可被视为一个宝库,从中汲取灵感以开发更有效的新疗法来治疗血管生成依赖性疾病。