Russell S M, Johnston J A, Noguchi M, Kawamura M, Bacon C M, Friedmann M, Berg M, McVicar D W, Witthuhn B A, Silvennoinen O
Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, Bethesda, MD 20892.
Science. 1994 Nov 11;266(5187):1042-5. doi: 10.1126/science.7973658.
Interleukin-2 (IL-2) signaling requires the dimerization of the IL-2 receptor beta.(IL-2R beta) and common gamma (gamma c) chains. Mutations of gamma c can result in X-linked severe combined immunodeficiency (XSCID). IL-2, IL-4, IL-7 (whose receptors are known to contain gamma c), and IL-9 (whose receptor is shown here to contain gamma c) induced the tyrosine phosphorylation and activation of the Janus family tyrosine kinases Jak1 and Jak3. Jak1 and Jak3 associated with IL-2R beta and gamma c, respectively; IL-2 induced Jak3-IL-2R beta and increased Jak3-gamma c associations. Truncations of gamma c, and a gamma c, point mutation causing moderate X-linked combined immunodeficiency (XCID), decreased gamma c-Jak3 association. Thus, gamma c mutations in at least some XSCID and XCID patients prevent normal Jak3 activation, suggesting that mutations of Jak3 may result in an XSCID-like phenotype.
白细胞介素-2(IL-2)信号传导需要白细胞介素-2受体β(IL-2Rβ)和共同γ链(γc)的二聚化。γc的突变可导致X连锁严重联合免疫缺陷症(XSCID)。IL-2、IL-4、IL-7(已知其受体含有γc)和IL-9(此处显示其受体含有γc)可诱导Janus家族酪氨酸激酶Jak1和Jak3的酪氨酸磷酸化及激活。Jak1和Jak3分别与IL-2Rβ和γc相关联;IL-2诱导Jak3与IL-2Rβ结合并增加Jak3与γc的结合。γc的截短以及导致中度X连锁联合免疫缺陷症(XCID)的γc点突变会减少γc与Jak3的结合。因此,至少一些XSCID和XCID患者中的γc突变会阻止Jak3的正常激活,这表明Jak3的突变可能导致类似XSCID的表型。