Tsunoda H, Terasawa T, Yageta M, Nakajima T, Tomooka Y, Tsuchida N, Oda K
Department of Biological Science and Technology, Science University of Tokyo, 2641 Yamazaki, Noda, 278, Japan.
Biochem Biophys Res Commun. 1999 Feb 24;255(3):722-30. doi: 10.1006/bbrc.1999.0143.
The sensitivities of apoptosis induced by E1A, c-Myc, Bax, and Nip3 to wild-type (wt) and mutated p53 and Id proteins were analyzed by transient transfection followed by flow cytometry with p53 null mouse cerebellum cell lines W7 and M13 that express wt and mutated p53 in response to dexamethasone, respectively. Apoptosis induced by c-Myc was stimulated weakly by wt p53, strongly by Ids, but suppressed completely by mutated p53 irrespective of coexpression with Ids, while apoptosis induced by E1A was suppressed by mutated p53 but stimulated when coexpressed with Ids. Apoptosis induced by Bax was little affected by wt and mutated p53, but inhibited by Ids, while apoptosis induced by Nip3 was inhibited by both wt and mutated p53 and inhibition was stimulated by Ids. Caspase-1 was activated only by Bax significantly when coexpressed with mutated p53 but not with wt p53. These results indicate that the apoptotic processes elicited by these inducers are different and differently affected by wt and mutated p53 and by Ids.
通过瞬时转染,随后使用p53基因缺失的小鼠小脑细胞系W7和M13进行流式细胞术分析,研究E1A、c-Myc、Bax和Nip3诱导的凋亡对野生型(wt)和突变型p53以及Id蛋白的敏感性,W7和M13细胞系分别在给予地塞米松后表达wt和突变型p53。c-Myc诱导的凋亡受到wt p53的微弱刺激、Ids的强烈刺激,但无论是否与Ids共表达,均被突变型p53完全抑制;而E1A诱导的凋亡受到突变型p53的抑制,但与Ids共表达时则受到刺激。Bax诱导的凋亡受wt和突变型p53的影响较小,但受到Ids的抑制;Nip3诱导的凋亡受到wt和突变型p53的抑制,且Ids可增强这种抑制作用。当与突变型p53共表达时,Caspase-1仅被Bax显著激活,与wt p53共表达时则未被激活。这些结果表明,这些诱导剂引发的凋亡过程不同,且受到wt和突变型p53以及Ids的影响也不同。