Vachon Pierre H
Département d'Anatomie et de Biologie Cellulaire, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC, Canada J1H5N4.
J Signal Transduct. 2011;2011:738137. doi: 10.1155/2011/738137. Epub 2011 Jul 13.
Cell survival and apoptosis implicate an increasing complexity of players and signaling pathways which regulate not only the decision-making process of surviving (or dying), but as well the execution of cell death proper. The same complex nature applies to anoikis, a form of caspase-dependent apoptosis that is largely regulated by integrin-mediated, cell-extracellular matrix interactions. Not surprisingly, the regulation of cell survival, apoptosis, and anoikis furthermore implicates additional mechanistic distinctions according to the specific tissue, cell type, and species. Incidentally, studies in recent years have unearthed yet another layer of complexity in the regulation of these cell processes, namely, the implication of cell differentiation state-specific mechanisms. Further analyses of such differentiation state-distinct mechanisms, either under normal or physiopathological contexts, should increase our understanding of diseases which implicate a deregulation of integrin function, cell survival, and anoikis.
细胞存活与凋亡涉及越来越复杂的参与者和信号通路,这些不仅调节存活(或死亡)的决策过程,还调节细胞死亡的实际执行。同样复杂的性质也适用于失巢凋亡,这是一种半胱天冬酶依赖性凋亡形式,在很大程度上受整合素介导的细胞与细胞外基质相互作用的调节。毫不奇怪,根据特定的组织、细胞类型和物种,细胞存活、凋亡和失巢凋亡的调节还涉及其他机制差异。顺便说一句,近年来的研究揭示了这些细胞过程调节中另一层复杂性,即细胞分化状态特异性机制的影响。在正常或生理病理背景下对这种分化状态不同机制的进一步分析,应该会增进我们对涉及整合素功能失调、细胞存活和失巢凋亡的疾病的理解。