Romer Lewis H, Birukov Konstantin G, Garcia Joe G N
Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287-4904, USA.
Circ Res. 2006 Mar 17;98(5):606-16. doi: 10.1161/01.RES.0000207408.31270.db.
The vascular wall contains intimal endothelium and medial smooth muscle that act as contiguous tissues with tight spatial and functional coordination in response to tonic and episodic input from the bloodstream and the surrounding parenchyma. Focal adhesions are molecular bridges between the intracellular and extracellular spaces that integrate a variety of environmental stimuli and mediate 2-way crosstalk between the extracellular matrix and the cytoskeleton. Focal adhesion components are targets for biochemical and mechanical stimuli that evoke crucial developmental and injury response mechanisms including cell growth, movement, and differentiation, and tailoring of the extracellular microenvironment. Focal adhesions provide the vascular wall constituents with flexible and specific tools for exchanging cues in a complex system. The molecular mechanisms that underlie these vital communications are detailed in this review with the goal of defining future targets for vascular tissue engineering and for the therapeutic modulation of disordered vascular growth, inflammation, thrombosis, and angiogenesis.
血管壁包含内膜内皮和中膜平滑肌,它们作为连续的组织,在对来自血流和周围实质的持续性和间歇性输入做出反应时,具有紧密的空间和功能协调性。粘着斑是细胞内和细胞外空间之间的分子桥梁,整合各种环境刺激,并介导细胞外基质和细胞骨架之间的双向串扰。粘着斑成分是生化和机械刺激的靶点,这些刺激引发关键的发育和损伤反应机制,包括细胞生长、运动和分化,以及细胞外微环境的调整。粘着斑为血管壁成分提供了在复杂系统中交换信号的灵活且特定的工具。本综述详细阐述了这些重要通讯背后的分子机制,目的是确定血管组织工程以及对紊乱的血管生长、炎症、血栓形成和血管生成进行治疗调节的未来靶点。