Fukada T, Hibi M, Yamanaka Y, Takahashi-Tezuka M, Fujitani Y, Yamaguchi T, Nakajima K, Hirano T
Department of Molecular Oncology, Biomedical Research Center, Osaka University Medical School, Japan.
Immunity. 1996 Nov;5(5):449-60. doi: 10.1016/s1074-7613(00)80501-4.
gp130 is a common signal transducer for the interleukin-6-related cytokines. To delineate the gp130-mediated growth signal, we established a series of pro-B cell lines expressing chimeric receptors composed of the extracellular domain of the granulocyte colony-stimulating factor receptor and the transmembrane and cytoplasmic domains of gp130. The second tyrosine (from the membrane) of gp130, which was required for the tyrosine phosphorylation of SHP-2, its association with GRB2, and activation of a MAP kinase, was essential for mitogenesis, but not for anti-apoptosis. On the other hand, the tyrosine in the YXXQ motifs essential for STAT3 activation was required for bcl-2 induction and anti-apoptosis. Furthermore, dominant-negative STAT3 inhibited anti-apoptosis. These data demonstrate that two distinct signals, mitogenesis and anti-apoptosis, are required for gp130-induced cell growth and that STAT3 is involved in anti-apoptosis.
gp130是白细胞介素-6相关细胞因子的共同信号转导子。为了阐明gp130介导的生长信号,我们建立了一系列表达嵌合受体的前B细胞系,这些嵌合受体由粒细胞集落刺激因子受体的胞外结构域以及gp130的跨膜和胞质结构域组成。gp130的第二个酪氨酸(从膜算起)对于SHP-2的酪氨酸磷酸化、其与GRB2的结合以及MAP激酶的激活是必需的,该酪氨酸对于有丝分裂是必不可少的,但对于抗凋亡并非必需。另一方面,STAT3激活所必需的YXXQ基序中的酪氨酸对于bcl-2诱导和抗凋亡是必需的。此外,显性负性STAT3抑制抗凋亡。这些数据表明,gp130诱导的细胞生长需要两种不同的信号,即有丝分裂和抗凋亡,并且STAT3参与抗凋亡。