Mikalsen S O, Husøy T, Vikhamar G, Sanner T
Laboratory for Environmental and Occupational Cancer, Institute for Cancer Research, The Norwegian Radium Hospital, Oslo.
FEBS Lett. 1997 Jan 20;401(2-3):271-5. doi: 10.1016/s0014-5793(96)01489-5.
The protein-tyrosine phosphatase inhibitors pervanadate, permolybdate, H2O2, and to a much lesser extent vanadate, increased the amount of cellular phosphotyrosine and induced tyrosine phosphorylation of connexin43 (Cx43) in early passage hamster embryo fibroblasts. The presence of phosphotyrosine in Cx43 immunoprecipitates from pervanadate-treated cells was shown by a phosphotyrosine-specific antibody and a phosphotyrosine-specific phosphatase. Pervanadate-induced Cx43 tyrosine phosphorylation was further verified by phosphoamino acid analysis, while no phosphotyrosine was present in control cells. This is the first observation of tyrosine phosphorylation of connexins in normal cells.
蛋白酪氨酸磷酸酶抑制剂过氧钒酸盐、过钼酸盐、过氧化氢,以及程度小得多的钒酸盐,增加了原代仓鼠胚胎成纤维细胞中细胞磷酸酪氨酸的量,并诱导了连接蛋白43(Cx43)的酪氨酸磷酸化。通过磷酸酪氨酸特异性抗体和磷酸酪氨酸特异性磷酸酶显示,在过氧钒酸盐处理的细胞的Cx43免疫沉淀物中存在磷酸酪氨酸。磷酸氨基酸分析进一步证实了过氧钒酸盐诱导的Cx43酪氨酸磷酸化,而对照细胞中不存在磷酸酪氨酸。这是在正常细胞中首次观察到连接蛋白的酪氨酸磷酸化。