Eastman A
Department of Pharmacology and Toxicology, Dartmouth Medical School, Hanover, New Hampshire 03755, USA.
Methods Cell Biol. 1995;46:41-55. doi: 10.1016/s0091-679x(08)61923-8.
The methods described here facilitate assessment of the DNA digestion that was once considered a hallmark of apoptosis, but is now recognized as a common overdigestion of genomic DNA; less frequent breaks also lead to the morphological appearance of an apoptotic nucleus. Whatever level of DNA digestion occurs, it may be brought about by activity of one of a number of endonucleases. Whether one endonuclease is responsible in all cases of apoptosis or whether different endonucleases are responsible in various systems and circumstances remains unknown. In attempting to identify changes in ion concentrations that might activate these endonucleases, we have observed intracellular acidification to correlate with apoptosis consistently. This observation may have other implications since the acidification could be responsible for activating other proteins, such as proteases, which are also associated with apoptosis. The importance of such events to the onset of apoptosis remains to be fully established.
这里描述的方法有助于评估曾经被视为细胞凋亡标志的DNA消化,但现在被认为是基因组DNA的常见过度消化;较少见的断裂也会导致凋亡细胞核的形态出现。无论发生何种程度的DNA消化,都可能是由多种核酸内切酶之一的活性引起的。在所有细胞凋亡情况下是否由一种核酸内切酶负责,或者在不同系统和环境中是否由不同的核酸内切酶负责,仍然未知。在试图确定可能激活这些核酸内切酶的离子浓度变化时,我们观察到细胞内酸化与细胞凋亡始终相关。这一观察结果可能还有其他含义,因为酸化可能负责激活其他蛋白质,如蛋白酶,它们也与细胞凋亡有关。此类事件对细胞凋亡起始的重要性仍有待充分确定。