Deparment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
FEBS J. 2010 Oct;277(19):3876-89. doi: 10.1111/j.1742-4658.2010.07798.x. Epub 2010 Aug 31.
Proteolytic processes in the extracellular matrix are a major influence on cell adhesion, migration, survival, differentiation and proliferation. The syndecan cell-surface proteoglycans are important mediators of cell spreading on extracellular matrix and respond to growth factors and other biologically active polypeptides. The ectodomain of each syndecan is constitutively shed from many cultured cells, but is accelerated in response to wound healing and diverse pathophysiological events. Ectodomain shedding is an important regulatory mechanism, because it rapidly changes surface receptor dynamics and generates soluble ectodomains that can function as paracrine or autocrine effectors, or competitive inhibitors. It is known that the family of syndecans can be shed by a variety of matrix proteinase, including many metzincins. Shedding is particularly active in proliferating and invasive cells, such as cancer cells, where cell-surface components are continually released. Here, recent research into the shedding of syndecans and its physiological relevance are assessed.
细胞外基质中的蛋白水解过程对细胞黏附、迁移、存活、分化和增殖有重要影响。黏附素细胞表面蛋白聚糖是细胞在细胞外基质上扩展的重要介质,对生长因子和其他生物活性多肽有反应。每个黏附素的细胞外结构域都从许多培养细胞中连续脱落,但在对伤口愈合和各种病理生理事件的反应中会加速脱落。细胞外结构域脱落是一种重要的调节机制,因为它可以快速改变表面受体的动态,并产生可溶性细胞外结构域,这些结构域可以作为旁分泌或自分泌效应物,或竞争性抑制剂发挥作用。已知黏附素家族可以被多种基质蛋白酶(包括许多金属蛋白酶)脱落。脱落特别活跃于增殖和侵袭性细胞,如癌细胞,细胞表面成分不断释放。在这里,评估了黏附素的脱落及其生理相关性的最新研究。