Bhalla A K, Amento E P, Serog B, Glimcher L H
J Immunol. 1984 Oct;133(4):1748-54.
The proliferative response of murine spleen and thymus cells to antigen but not to lectin was inhibited by the active metabolite of vitamin D3, 1,25-(OH)2D3. To directly examine the effect of 1,25-(OH)2D3 on T cell activation in the absence of other complicating interactions, we utilized a panel of cloned Ia-restricted T cell hybridomas that secrete IL 2 on activation by cloned Ia-bearing stimulator cells (TA3) or when stimulated by mitogen. Physiologic concentrations of 1,25-(OH)2D3 (0.01 to 0.1 nm) inhibited the antigen-induced secretion of IL 2 by several of these T cell hybridomas. This inhibition was dependent on the concentration of the free hormone and could be overcome by increasing the number of Ia-bearing stimulator cells used. Pretreatment of the T hybridoma but not the TA3 stimulator cell with 1,25-(OH)2D3 resulted in inhibition of activation. These results are consistent with the finding that specific 1,25-(OH)2D3 receptors are present on the T cell hybridomas but are lacking in TA3 cells. 1,25-(OH)2D3 failed, however, to inhibit the activation of the T cell hybridomas by lectin or by an anti-Thy-1 antibody. These findings suggest that 1,25-(OH)2D3 may be interfering with early events of antigen-induced T cell activation, perhaps by hindering T cell recognition of the relevant antigen on stimulator cell surfaces. This system should prove useful in studying the molecular mechanisms by which 1,25-(OH)2D3 acts to inhibit T cell activation and subsequent IL 2 production.
维生素D3的活性代谢产物1,25-(OH)2D3可抑制小鼠脾脏和胸腺细胞对抗原而非凝集素的增殖反应。为了在不存在其他复杂相互作用的情况下直接检测1,25-(OH)2D3对T细胞激活的影响,我们使用了一组克隆的Ia限制性T细胞杂交瘤,这些杂交瘤在被携带Ia的克隆刺激细胞(TA3)激活时或被丝裂原刺激时会分泌白细胞介素2(IL 2)。生理浓度的1,25-(OH)2D3(0.01至0.1纳米)可抑制其中几种T细胞杂交瘤抗原诱导的IL 2分泌。这种抑制作用取决于游离激素的浓度,并且可以通过增加所用携带Ia的刺激细胞数量来克服。用1,25-(OH)2D3预处理T杂交瘤而非TA3刺激细胞会导致激活受到抑制。这些结果与以下发现一致,即T细胞杂交瘤上存在特异性的1,25-(OH)2D3受体,而TA3细胞中则没有。然而,1,25-(OH)2D3未能抑制凝集素或抗Thy-1抗体对T细胞杂交瘤的激活。这些发现表明,1,25-(OH)2D3可能正在干扰抗原诱导的T细胞激活的早期事件,也许是通过阻碍T细胞对刺激细胞表面相关抗原的识别。该系统应有助于研究1,25-(OH)2D3抑制T细胞激活及随后IL 2产生的分子机制。