So H S, Park R K, Kim M S, Lee S R, Jung B H, Chung S Y, Jun C D, Chung H T
Department of Microbiology & Immunology, Wonkwang University School of Medicine, Iksan Chonbuk, South Korea.
Biochem Biophys Res Commun. 1998 Jun 29;247(3):809-13. doi: 10.1006/bbrc.1998.8788.
S-nitrosylation by S-nitrosoglutathione (GSNO), a nitric oxide (NO) donor, suppresses the phosphotransferase activity of cJun N-terminal kinase 2 (JNK2)/stress activated protein kinase (SAPK) in dose- and time-dependent manners in vitro. JNK2 activity is significantly decreased at 10 microM of GSNO, which is dramatically reversed by adding 10 mM of DTT. Reduced form of glutathione protects the GSNO-induced suppression of JNK2 activation in a dose-dependent fashion. However, GSNO-treated Sek1 does not affect the JNK2 activity of phosphotransferation toward c-Jun N-terminal1-79 protein. These results indicate that NO may exert a regulatory role of JNK2 activity by S-nitrosylation of the protein in apoptotic signaling pathway. Suppression of JNK2 phosphotransferase activity by NO is also supported by the observation that NO plays an important anti-apoptotic roles in heptocytes, splenocytes, eosinophils and B lymphocytes.
一氧化氮供体S-亚硝基谷胱甘肽(GSNO)介导的S-亚硝基化作用,在体外以剂量和时间依赖的方式抑制c-Jun氨基末端激酶2(JNK2)/应激激活蛋白激酶(SAPK)的磷酸转移酶活性。在10微摩尔的GSNO作用下,JNK2活性显著降低,而添加10毫摩尔的二硫苏糖醇(DTT)可显著逆转这一现象。还原型谷胱甘肽以剂量依赖的方式保护GSNO诱导的JNK2激活抑制作用。然而,经GSNO处理的Sek1并不影响JNK2对c-Jun N末端1-79蛋白的磷酸转移活性。这些结果表明,在凋亡信号通路中,一氧化氮可能通过对该蛋白的S-亚硝基化作用发挥对JNK2活性的调节作用。一氧化氮对JNK2磷酸转移酶活性的抑制作用,也得到了以下观察结果的支持:一氧化氮在肝细胞、脾细胞、嗜酸性粒细胞和B淋巴细胞中发挥重要的抗凋亡作用。