Kosaka H, Ogata M, Hikita I, Maruo S, Sugihara S, Matsubara H, Takai Y, Hamaoka T, Fujiwara H
Biomedical Research Center, Osaka University Medical School, Japan.
Proc Natl Acad Sci U S A. 1989 May;86(10):3773-7. doi: 10.1073/pnas.86.10.3773.
A thymic stromal cell clone, MRL104.8a, expresses class I as well as class II H-2k antigens after exposure to gamma-interferon. This clone also produces thymic stroma-derived T-cell growth factor (TSTGF), which is distinct from other known interleukins and is capable of promoting the growth of various antigen-specific helper T cell (Th) clones without requiring a specific antigen or interleukin 2. When the keyhole limpet hemocyanin (KLH)-specific, I-Ek-restricted Th clone 9-16 was cultured on an Ia (I-Ak and I-Ek)-expressing MRL104.8a monolayer, potent proliferation of the 9-16 cells was induced by TSTGF produced by the monolayer. In contrast, the addition of KLH resulted in lethal growth inhibition of Th clone 9-16 cells. Another Th clone that is KLH-specific but I-Ab-restricted was capable of proliferating on the Iak-expressing MRL104.8a monolayer whether or not KLH was present. More importantly, death of Th clone 9-16 cells cultured on a MRL104.8a monolayer in the presence of KLH was almost completely prevented by the addition of anti-I-Ek or anti-CD3 monoclonal antibodies, which are capable of blocking antigen recognition by the T-cell receptor. However, when Th clone 9-16 cells were cultured in the presence of KLH but on a monolayer of MRL28.8a cells, another thymic stromal clone that expresses a comparable amount of I-Ek antigen but produces a marginal amount of TSTGF, cells did not die; a lethal effect was induced by adding TSTGF. These results indicate that the TSTGF-producing and Ia-expressing thymic stromal cells induce the continuous proliferation or selective elimination of each T-cell clone, depending on whether the T-cell receptor is stimulated by the relevant antigen associated with Ia molecules expressed on the stromal cell surface.
一个胸腺基质细胞克隆MRL104.8a,在暴露于γ干扰素后表达I类以及II类H-2k抗原。该克隆还产生胸腺基质衍生的T细胞生长因子(TSTGF),它不同于其他已知的白细胞介素,能够促进各种抗原特异性辅助性T细胞(Th)克隆的生长,而无需特定抗原或白细胞介素2。当在表达Ia(I-Ak和I-Ek)的MRL104.8a单层细胞上培养血蓝蛋白(KLH)特异性、I-Ek限制性的Th克隆9-16时,单层细胞产生的TSTGF诱导了9-16细胞的强烈增殖。相反,添加KLH导致Th克隆9-16细胞的致死性生长抑制。另一个KLH特异性但I-Ab限制性的Th克隆,无论是否存在KLH,都能够在表达Iak的MRL104.8a单层细胞上增殖。更重要的是,在存在KLH的情况下,在MRL104.8a单层细胞上培养的Th克隆9-16细胞的死亡几乎完全被添加抗I-Ek或抗CD3单克隆抗体所阻止,这些抗体能够阻断T细胞受体对抗原的识别。然而,当Th克隆9-16细胞在存在KLH的情况下,但在MRL28.8a细胞单层上培养时,另一个胸腺基质克隆表达相当数量的I-Ek抗原但产生少量的TSTGF,细胞没有死亡;添加TSTGF诱导了致死效应。这些结果表明,产生TSTGF并表达Ia的胸腺基质细胞根据T细胞受体是否受到与基质细胞表面表达的Ia分子相关的相关抗原的刺激,诱导每个T细胞克隆的持续增殖或选择性消除。