Avraham A, Jung S, Samuels Y, Seger R, Ben-Neriah Y
Lautenberg Center for General and Tumor Immunology, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.
Eur J Immunol. 1998 Aug;28(8):2320-30. doi: 10.1002/(SICI)1521-4141(199808)28:08<2320::AID-IMMU2320>3.0.CO;2-K.
Previously we implicated c-Jun N-terminal kinase (JNK) as an element that is involved in signal integration during co-stimulation of T lymphocytes. This pathway has now been traced to an upper level, comprising MAPKK SEK1/MKK4/JNKK1 which, similarly to JNK, must receive input both from the TCR and CD28. A large portion of this input is probably integrated at the level of the Rho-family protein CDC42 which, here, activates SEK1 and JNK to the level reached by TCR and CD28 stimulation. We have identified another putative SEK/ JNK pathway regulator, PKCtheta, which in contrast to CDC42, activates SEK and JNK maximally only in conjunction with a calcium signal delivered through calcineurin. Signals originating at the TCR and CD28 may travel down the JNK pathway via PKCtheta, calcineurin, CDC42, MEKK1 and SEK1.
此前我们认为c-Jun氨基末端激酶(JNK)是参与T淋巴细胞共刺激过程中信号整合的一个元件。现在这条信号通路已追溯到更上游的水平,包括丝裂原活化蛋白激酶激酶(MAPKK)SEK1/MKK4/JNKK1,它与JNK类似,必须同时接收来自T细胞受体(TCR)和CD28的信号输入。很大一部分这种信号输入可能在Rho家族蛋白CDC42水平整合,在此,CDC42将SEK1和JNK激活至TCR和CD28刺激所达到的水平。我们鉴定出另一种假定的SEK/JNK信号通路调节因子PKCtheta,与CDC42不同,它只有在与通过钙调神经磷酸酶传递的钙信号共同作用时,才能最大程度地激活SEK和JNK。源自TCR和CD28的信号可能通过PKCtheta、钙调神经磷酸酶、CDC42、丝裂原活化蛋白激酶激酶激酶1(MEKK1)和SEK1沿JNK信号通路传导。