Signaling via IL-2 and IL-4 in JAK3-deficient severe combined immunodeficiency lymphocytes: JAK3-dependent and independent pathways

被引:109
作者
Oakes, SA
Candotti, F
Johnston, JA
Chen, YQ
Ryan, JJ
Taylor, N
Liu, XW
Hennighausen, L
Notarangelo, LD
Paul, WE
Blaese, RM
OShea, JJ
机构
[1] NIH, NATL CTR HUMAN GENOME RES, CLIN GENE THERAPY BRANCH, BETHESDA, MD 20892 USA
[2] HOWARD HUGHES MED INST, NIH, RES SCHOLARS PROGRAM, BETHESDA, MD 20892 USA
[3] NIAID, IMMUNOL LAB, NIH, BETHESDA, MD 20892 USA
[4] NIDDKD, BIOCHEM & METAB LAB, NIH, BETHESDA, MD 20892 USA
[5] CHILDRENS HOSP LOS ANGELES, DIV RES IMMUNOL & BONE MARROW TRANSPLANTAT, LOS ANGELES, CA 90027 USA
[6] UNIV BRESCIA, DEPT PEDIAT, I-25123 BRESCIA, ITALY
[7] NIAMSD, NIH, ARTHRIT & RHEUMATISM BRANCH, LYMPHOCYTE CELL BIOL SECT, BETHESDA, MD 20892 USA
关键词
D O I
10.1016/S1074-7613(00)80274-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Both IL-2 and IL-4 bind to receptors containing the common gamma chain and JAK3. Although JAK3 is required for proper lymphoid development, the precise roles of this kinase in IL-2 and IL-4 signaling in lymphocytes have not been defined. Here, we have studied IL-2 and IL-4 signaling in B cell lines lacking JAK3. Although IL-2-induced phosphorylation of IL-2R beta, JAK1, and STAT5 all required the presence of JAK3, IL-4-mediated phosphorylation of JAK1, STAT6, and insulin receptor substrates 1 and 2 did not. However, IL-4-induced effects were clearly improved following JAK3 expression. These data indicate that IL-4 signaling occurs in the absence of of JAK3, but is comparatively inefficient. These findings may help in understanding the pathogenesis of the immunodeficiency that occurs with mutations of JAK3 and may suggest a mechanism for the pleiotropic effects of IL-4.
引用
收藏
页码:605 / 615
页数:11
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