Kanagawa O
J Immunol. 1983 Aug;131(2):606-10.
The requirement for the signals in induction of cytolytic T lymphocytes (CTL) has been investigated. C57BL/6 X CBA/T6 F1 spleen cells stimulated with the lectin leukoagglutinin (L-A) failed to show CTL activity in a PHA-facilitated assay, although L-A-activated splenic T cells were able to respond to T cell growth factor (TCGF). Concanavalin A (Con A) on the other hand was able to induce cytolytic activity from CTL-P, as well as to render splenic T cells responsive to TCGF. Furthermore, L-A-activated splenic T cells could generate cytolytic activity upon subsequent culture in secondary mixed leukocyte culture supernatant (2 degrees MLC SN). In contrast, EL-4-derived SN (EL-4 SN) was unable to induce cytolytic activity from L-A-activated spleen cells. In addition, proliferation of L-A-activated spleen cells cultured in EL-4 SN was similar to those cultured in 2 degrees MLC SN. Nonactivated spleen cells were totally unresponsive to both SN in proliferation and generation of CTL. Analysis of T cell clones for the production of a factor necessary for induction of cytolytic activity revealed that both cytolytic and noncytolytic T cell clones were able to produce a factor(s) for the generation of cytolytic activity from L-A-activated T cells. On the other hand, SN from certain antigen-stimulated T cell clones produced factors capable of inducing cytocytic activity by L-A-activated T cells only in the presence of EL-4 SN. Neither EL-4 SN nor cloned T cell SN alone had such a capacity. The nature of the necessary lymphokines in the SN from the clone cells or from the EL-4 is unknown. In the case of the EL-4 SN, it is not known whether the presence of TCGF plays a role or whether that role is perhaps more differentiative than proliferative. This study provides evidence that the induction of CTL from CTL-P can be dissociated into activation, which is required to render T cells responsive to second signals, and differentiation, which is mediated by two different factors.
对诱导细胞毒性T淋巴细胞(CTL)所需信号进行了研究。用凝集素白细胞凝集素(L-A)刺激的C57BL/6×CBA/T6 F1脾细胞,在PHA促进的试验中未能显示出CTL活性,尽管L-A激活的脾T细胞能够对T细胞生长因子(TCGF)作出反应。另一方面,伴刀豆球蛋白A(Con A)能够从CTL-P诱导细胞溶解活性,也能使脾T细胞对TCGF作出反应。此外,L-A激活的脾T细胞在随后的二级混合白细胞培养上清液(2°MLC SN)中培养时可产生细胞溶解活性。相比之下,EL-4来源的SN(EL-4 SN)不能从L-A激活的脾细胞诱导细胞溶解活性。此外,在EL-4 SN中培养的L-A激活的脾细胞的增殖与在2°MLC SN中培养的细胞相似。未激活的脾细胞对两种SN在增殖和CTL产生方面完全无反应。对产生诱导细胞溶解活性所需因子的T细胞克隆进行分析发现,细胞溶解和非细胞溶解T细胞克隆都能够产生使L-A激活的T细胞产生细胞溶解活性的因子。另一方面,某些抗原刺激的T细胞克隆的SN仅在存在EL-4 SN的情况下产生能够诱导L-A激活的T细胞产生细胞毒性活性的因子。单独的EL-4 SN或克隆的T细胞SN都没有这种能力。克隆细胞或EL-4的SN中必需淋巴因子的性质尚不清楚。就EL-4 SN而言,尚不清楚TCGF的存在是否起作用,或者该作用是否可能更多地是分化作用而非增殖作用。这项研究提供了证据,表明从CTL-P诱导CTL可分为激活(使T细胞对第二信号作出反应所必需)和分化(由两种不同因子介导)。