Levy R R, Cordonier H, Czyba J C, Guerin J F
Laboratoire de Biologie de la Reproduction du Pr. J.L. Laurent, Hôpital Nord, Saint Ertienne, France.
Ital J Anat Embryol. 2001;106(2 Suppl 2):101-8.
The presence of dead cells in the preimplantation mammalian embryo has been well described. Since Kerr et al. (1972), it has become apparent that these cells die by apoptosis, a form of programmed cell death. This review analyses the recent morphological and biochemical evidence that apoptosis play a role in early mammalian embryo development. Normal and apoptotic (i.e. fragmented) embryos express several apoptosis-related genes during mammalian preimplantation embryo development, with severe changes when apoptosis is activated; these findings support a model in which mammalian preimplantation embryo development is regulated by the ratio of pro- and -anti- apoptotic genes. Apoptosis may be a normal feature in human preimplantation development, even in vivo, and may play an active role in the developing embryo through the removal of genetically abnormal cells. Contrary to these beneficial effects, apoptosis may have detrimental effects if either the number of apoptotic cells or ratio of these cells to the normal cells is elevated. According to this value, embryos could either continue to develop or arrest.
植入前哺乳动物胚胎中存在死亡细胞已得到充分描述。自克尔等人(1972年)以来,很明显这些细胞通过凋亡死亡,这是一种程序性细胞死亡形式。本综述分析了近期关于凋亡在早期哺乳动物胚胎发育中起作用的形态学和生化证据。正常胚胎和凋亡(即碎片化)胚胎在哺乳动物植入前胚胎发育过程中表达几种与凋亡相关的基因,当凋亡被激活时会发生严重变化;这些发现支持了一种模型,即哺乳动物植入前胚胎发育受促凋亡基因和抗凋亡基因比例的调节。凋亡可能是人类植入前发育中的一个正常特征,即使在体内也是如此,并且可能通过清除基因异常细胞在发育中的胚胎中发挥积极作用。与这些有益作用相反,如果凋亡细胞数量或这些细胞与正常细胞的比例升高,凋亡可能会产生有害影响。根据这个值,胚胎可能会继续发育或停滞。