Nakamura M, Takasawa N, Ohbo K, Higashimura N, Ohtani K, Tanaka Y, Sugamura K
Human Gene Sciences Center, Tokyo Medical and Dental University, Japan.
Leukemia. 1997 Apr;11 Suppl 3:7-9.
We have cloned two genes for cell surface molecules, capable of delivering the intracellular signals, which are modulated for their expression by Tax. One is the gamma chain of the interleukin-2 (IL-2) receptor which is suggested to be critical for IL-2-dependent growth of human T-cell leukemia virus type I (HTLV-I) infected cells. The gamma chain is upregulated by Tax, like the IL-2 receptor alpha chain. This upregulation may compensate the gamma chain downregulation after IL-2 binding, presumably resulting in more frequent growth of HTLV-I infected T cells. The other is gp34 that was initially identified as a molecule specifically expressed on HTLV-I-infected T cells. gp34 has been demonstrated to bind OX40 which belongs to the tumor necrosis factor (TNF) receptor family. We found that HTLV-I Tax induces expression of gp34 and OX40, and that normal T cell transiently express both gp34 and OX40 upon antigenic stimulation. Collectively, it may be possible that HTLV-I-infected T cells are in a predisposition to growth due to modulated expression by HTLV-I Tax of gp34/OX40 and the gamma chain.
我们克隆了两个编码细胞表面分子的基因,这些分子能够传递细胞内信号,其表达受Tax调节。其中一个是白细胞介素-2(IL-2)受体的γ链,它被认为对I型人类T细胞白血病病毒(HTLV-I)感染细胞的IL-2依赖性生长至关重要。γ链像IL-2受体α链一样被Tax上调。这种上调可能补偿IL-2结合后γ链的下调,大概会导致HTLV-I感染的T细胞更频繁地生长。另一个是gp34,它最初被鉴定为在HTLV-I感染的T细胞上特异性表达的分子。已证明gp34能结合属于肿瘤坏死因子(TNF)受体家族的OX40。我们发现HTLV-I Tax诱导gp34和OX40的表达,并且正常T细胞在抗原刺激后会短暂表达gp34和OX40。总体而言,由于HTLV-I Tax对gp34/OX40和γ链的表达调节,HTLV-I感染的T细胞可能易于生长。