Matsumoto H, Shimura M, Omatsu T, Okaichi K, Majima H, Ohnishi T
Department of Biology, Nara Medical University, Japan.
Cancer Lett. 1994 Nov 25;87(1):39-46. doi: 10.1016/0304-3835(94)90407-3.
We investigated the accumulation of p53 proteins after heat stress and their association with HSP72/HSC73 using four human glioblastoma cell lines. Human glioblastoma cell lines U-87MG and A-172 exhibited no mutation in the region between the 2nd and 11th exons of the p53 gene, whereas A-7 and T98G had mutations in exon 5 and exon 7 of the p53 gene, respectively. In U-87MG and A-172, the levels of wild-type p53 protein were slightly increased by heat stress. Levels of mutant p53 protein were apparently increased by heat stress in A-7, but not in T98G. Furthermore, wild-type p53 proteins in both U-87MG and A-172 co-immunoprecipitated with anti-HSP72/HSC73 antibody and HSP72 and HSC73 in them co-immunoprecipitated with anti-p53 antibody as did the mutant p53 proteins. These findings suggest that p53 proteins accumulated by heat stress are associated with HSP72 and HSC73.
我们使用四种人胶质母细胞瘤细胞系,研究了热应激后p53蛋白的积累情况及其与HSP72/HSC73的关联。人胶质母细胞瘤细胞系U-87MG和A-172在p53基因第2外显子和第11外显子之间的区域未表现出突变,而A-7和T98G分别在p53基因的第5外显子和第7外显子存在突变。在U-87MG和A-172中,野生型p53蛋白水平因热应激而略有增加。在A-7中,突变型p53蛋白水平因热应激而明显增加,但在T98G中未增加。此外,U-87MG和A-172中的野生型p53蛋白均与抗HSP72/HSC73抗体发生共免疫沉淀,其中的HSP72和HSC73也与抗p53抗体发生共免疫沉淀,突变型p53蛋白也是如此。这些发现表明,热应激积累的p53蛋白与HSP72和HSC73相关。