Dunnebacke T H, Walen K H
Viral and Rickettsial Disease Laboratory, California Department of Health Services, Berkeley 94704-1011, USA.
In Vitro Cell Dev Biol Anim. 1999 May;35(5):252-61. doi: 10.1007/s11626-999-0069-6.
Exposure for less than an hour to a protein isolated from Naegleria amoebae initiates a process that has no apparent effect on the appearance or growth of chick embryo or CHO cell cultures for 4 to 9 days; after the development of confluency, at some unknown signal, all of the cells undergo an apoptotic death within a 12- to 24-hour period. Abnormalities detected among the last mitotic cells include chromosomal breakage and early reversal in metaphase to telo/interphase daughter nuclei with irregular shapes. Additional events in the dying cultures include the development of a cytoplasmic amoebic-related immunogen, gross DNA fragmentation, cell blebbing, shrinkage, and apoptotic body formation. Culture death included all cells, those present in confluent cultures when the protein was added, and in other cultures, those formed during a more than 30-fold increase in cells as the cultures became confluent. The increase in the number of cells followed by the uniformity and synchrony of their death pattern indicates that the signal to kill has increased and spread throughout the culture; upon an unknown condition related to confluency, events are initiated that lead to the unusual apoptotic death of the culture.
暴露于从耐格里属变形虫分离出的一种蛋白质不到一小时,会启动一个过程,该过程在4至9天内对鸡胚或CHO细胞培养物的外观或生长没有明显影响;在细胞汇合后,在某个未知信号的作用下,所有细胞会在12至24小时内经历凋亡死亡。在最后一批有丝分裂细胞中检测到的异常包括染色体断裂以及中期到末期/间期子核的早期逆转,子核形状不规则。垂死培养物中的其他事件包括形成一种与细胞质变形虫相关的免疫原、大量DNA片段化、细胞起泡、收缩以及凋亡小体形成。培养物死亡包括所有细胞,即添加蛋白质时汇合培养物中存在的细胞,以及在其他培养物中,随着培养物汇合细胞数量增加超过30倍期间形成的细胞。细胞数量的增加以及随后其死亡模式的一致性和同步性表明,致死信号增强并在整个培养物中传播;在与汇合相关的未知条件下,会引发导致培养物异常凋亡死亡的事件。