Kumaki S, Ochs H D, Kuropatwinski K K, Konno T, Timour M S, Cosman D, Baumann H
Department of Pediatrics, University of Washington, Seattle, WA, USA.
Clin Exp Immunol. 1999 Feb;115(2):356-61. doi: 10.1046/j.1365-2249.1999.00792.x.
Mutations of the common gamma (gammac) chain result in X-linked SCID (X-SCID), which is characterized by the reduction in number or absence of peripheral blood T cells and natural killer (NK) cells, with retention of normal numbers of B cells. In the present study we describe a novel mutant gammac chain of an X-SCID patient with a typical X-SCID phenotype. This mutant receptor subunit is able to associate with Jak3 to transduce a weak signal. The Jak3-specific action is demonstrated by the induction of gene expression through the haematopoietin receptor response element (HRRE) by IL-2 and IL-4 in the experimental model of transiently transfected hepatoma cells over-expressing Jak3. This result suggests that a threshold in the gammac-Jak3 interaction determines the X-SCID phenotype.
共同γ(γc)链的突变导致X连锁重症联合免疫缺陷病(X-SCID),其特征是外周血T细胞和自然杀伤(NK)细胞数量减少或缺失,而B细胞数量正常。在本研究中,我们描述了一名具有典型X-SCID表型的X-SCID患者的新型突变γc链。这种突变受体亚基能够与Jak3结合以转导微弱信号。在过表达Jak3的瞬时转染肝癌细胞实验模型中,IL-2和IL-4通过造血受体反应元件(HRRE)诱导基因表达,证明了Jak3的特异性作用。该结果表明γc-Jak3相互作用中的一个阈值决定了X-SCID表型。