Golias C, Tsoutsi E, Matziridis A, Makridis P, Batistatou A, Charalabopoulos K
Department of Physiology, Clinical Unit, Medical Faculty, University of Ioannina, Greece.
In Vivo. 2007 Sep-Oct;21(5):757-69.
In multicellular organisms the development of adhesion bonds, either among cells or among cells and components of the extracellular matrix, is a crucial process. These interactions are mediated by molecules which are named adhesion molecules and play a main role both at the early stages of the development of tissue integrity and later. Cell adhesion molecules (CAMs) have a key role in several pathologies such as cancer and inflammatory diseases. Selectins, integrins and immunoglobulin gene superfamily of adhesion receptors mediate different steps of leukocyte migration from the bloodstream towards the inflammatory foci. Leukocyte interactions with the vascular endothelium are highly orchestrated processes that include the capture of free-flowing leukocytes from the blood with subsequent leukocyte rolling, arrest, firm adhesion and ensuing diapedesis. These interactions occur under high shear stresses within venules and depend on multiple families of adhesion molecules. As a response to infection mediators, leukocyte gathering is considered to be crucial for the adequate defence of the organism to any kind of injury or infection. Endothelial activation contributes significantly to the systemic inflammatory response to bacteraemia and increased expression. Release of soluble endothelial markers into the circulation has been demonstrated together with elevated plasma levels of CAMs and has been reported in bacteraemic patients. It has been proposed that infection of endothelial cells with Staphylococcus aureus, Streptococcus sanguis, or Staphylococcus epidermidis induces surface expression of ICAM-1 and VCAM-1 and monocyte adhesion. In general, leukocyte/endothelial cell interactions such as capture, rolling, and firm adhesion can no longer be viewed as occurring in discrete steps mediated by individual families of adhesion molecules but rather as a series of overlapping synergistic interactions among adhesion molecules resulting in an adhesion cascade. These cascades thereby direct leukocyte migration, which is essential for the generation of effective inflammatory responses and the development of rapid immune responses.
在多细胞生物中,细胞间或细胞与细胞外基质成分之间黏附键的形成是一个关键过程。这些相互作用由被称为黏附分子的分子介导,在组织完整性发育的早期和后期都发挥着主要作用。细胞黏附分子(CAMs)在多种病理状况如癌症和炎症性疾病中起关键作用。选择素、整合素和黏附受体免疫球蛋白基因超家族介导白细胞从血液流向炎症病灶的不同步骤。白细胞与血管内皮的相互作用是高度协调的过程,包括从血液中捕获自由流动的白细胞,随后白细胞滚动、停滞、牢固黏附并随之发生穿胞作用。这些相互作用发生在小静脉内的高剪切应力下,并且依赖于多个黏附分子家族。作为对感染介质的反应,白细胞聚集被认为对于机体充分抵御任何类型的损伤或感染至关重要。内皮细胞活化对菌血症的全身炎症反应和表达增加有显著贡献。可溶性内皮标志物释放到循环中已得到证实,同时菌血症患者血浆中CAMs水平升高也有报道。有人提出,金黄色葡萄球菌、血链球菌或表皮葡萄球菌感染内皮细胞会诱导细胞间黏附分子-1(ICAM-1)和血管细胞黏附分子-1(VCAM-1)的表面表达以及单核细胞黏附。一般来说,白细胞/内皮细胞相互作用,如捕获、滚动和牢固黏附,不再被视为由单个黏附分子家族介导的离散步骤,而是黏附分子之间一系列重叠的协同相互作用,从而产生黏附级联反应。这些级联反应进而指导白细胞迁移,这对于产生有效的炎症反应和快速免疫反应的发展至关重要。