Saini K S, Walker N I
Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Woolloongabba, Brisbane, Queensland, Australia.
Mol Cell Biochem. 1998 Jan;178(1-2):9-25. doi: 10.1023/a:1006891430596.
In eukaryotes, the regulation of tissue cell numbers is a critical homeostatic objective that is achieved through tight control of apoptosis, mitosis and differentiation. While much is known about the genetic regulation of cell growth and differentiation, the molecular basis of apoptosis is less well understood. Genes involved in both cell proliferation and apoptosis reflect the role of some stimuli in both of these processes, the cell response depending on the overall cellular milieu. Recent research has given fascinating insights into the complex genetic and molecular mechanisms regulating apoptosis. A picture is emerging of the initiation in certain cells, after an apoptotic trigger, of sequential gene expression and specific signal transduction cascades that guide cells along the cell death pathway. Changes in gene expression precede the better known biochemical and morphological changes of apoptosis. It seems possible that, as a result of increased understanding of the cellular events preceding cell death, apoptosis may become more amenable to manipulation by appropriate drug- and gene-based therapies.
在真核生物中,组织细胞数量的调节是一个关键的稳态目标,这是通过对细胞凋亡、有丝分裂和分化的严格控制来实现的。虽然人们对细胞生长和分化的基因调控了解很多,但细胞凋亡的分子基础却知之甚少。参与细胞增殖和凋亡的基因反映了某些刺激在这两个过程中的作用,细胞反应取决于整体细胞环境。最近的研究为调节细胞凋亡的复杂遗传和分子机制提供了引人入胜的见解。一幅图景正在浮现:在凋亡触发后,某些细胞中开始了顺序基因表达和特定信号转导级联反应,引导细胞沿着细胞死亡途径发展。基因表达的变化先于细胞凋亡中更为人所知的生化和形态学变化。由于对细胞死亡前细胞事件的了解增加,细胞凋亡似乎有可能更容易通过适当的基于药物和基因的疗法进行操控。