Steiner G, Wolff K, Pehamberger H, Stingl G
J Immunol. 1985 Feb;134(2):736-41.
The capacity of epidermal cells (EC) to stimulate T cell activation is a Langerhans cell (LC)-dependent phenomenon. In all in vitro assays probed, LC subserve antigen-presenting cell functions in that they display surface-bound foreign or altered-self structures and thereby activate T cell responses. In contrast, attempts to demonstrate accessory cell (ACC) function of LC-containing EC have yielded negative results, i.e., EC lacking foreign cell surface antigens were not able to restore cytotoxic T lymphocyte (CTL) responses in Ia+ adherent cell-depleted cultures. Reasoning that the ACC function of EC might be critically linked to cluster formation between LC and other cell types involved, we tested the ACC function of EC under experimental conditions that allow a close physical contact between the cell types involved (round-bottomed microtiter plates and brief centrifugation of culture plates). By using these modifications, the failure of highly purified B6 T cells to develop alloreactive CTL activity when stimulated with either highly purified, mitomycin C-treated C3H or B6CF1 T cells was restored by the addition of B6 EC. The CTL thus generated produced significant lysis of Con-A-stimulated C3H or BALB/c, but not B6, spleen cell targets. In a similar fashion, TNP- or FITC-specific CTL were generated when (in a syngeneic system) mitomycin C-treated TNP- or FITC-modified stimulator T cells and responder T cells were co-cultured in the presence, but not in the absence, of unmodified EC. The capacity of EC to restore CTL activity in a culture system depleted of Ia-bearing cells was not dependent upon their H-2 type, but was critically linked to the presence of Ia-bearing LC. We therefore conclude that LC-containing EC can subserve the ACC function in the generation of H-2-restricted CTL, provided that culture conditions are chosen that allow a close physical contact between the cell types involved.
表皮细胞(EC)刺激T细胞活化的能力是一种依赖朗格汉斯细胞(LC)的现象。在所有检测的体外试验中,LC发挥抗原呈递细胞的功能,因为它们展示表面结合的外来或自身改变的结构,从而激活T细胞反应。相比之下,试图证明含LC的EC的辅助细胞(ACC)功能的实验均得到阴性结果,即缺乏外来细胞表面抗原的EC无法在Ia⁺贴壁细胞耗尽的培养物中恢复细胞毒性T淋巴细胞(CTL)反应。考虑到EC的ACC功能可能与LC和其他相关细胞类型之间的簇形成密切相关,我们在允许相关细胞类型紧密物理接触的实验条件下(圆底微量滴定板和培养板短暂离心)测试了EC的ACC功能。通过这些改进,当用高度纯化的、经丝裂霉素C处理的C3H或B6CF1 T细胞刺激时,高度纯化的B6 T细胞无法产生同种异体反应性CTL活性,但加入B6 EC后可恢复。由此产生的CTL对Con - A刺激的C3H或BALB/c脾细胞靶标产生显著裂解,但对B6脾细胞靶标无裂解作用。以类似方式,当(在同基因系统中)经丝裂霉素C处理的TNP或FITC修饰的刺激T细胞和反应性T细胞在未修饰的EC存在而非不存在的情况下共培养时,可产生TNP或FITC特异性CTL。EC在缺乏Ia⁺细胞的培养系统中恢复CTL活性的能力不依赖于它们的H - 2类型,但与含Ia⁺的LC的存在密切相关。因此,我们得出结论,只要选择允许相关细胞类型紧密物理接触的培养条件,含LC的EC在H - 2限制的CTL产生过程中可发挥ACC功能。