Goldstein S A, Mescher M F
J Immunol. 1986 Dec 1;137(11):3383-92.
Novel cell-sized, supported artificial membranes bearing class I antigens have been prepared by a simple dialysis procedure and then used to study the requirements for antigen recognition by precursor cytotoxic T lymphocytes (CTL). The membranes were made by mixing lipid, H-2 antigen, and C18 alkylated 5 microns silica beads in deoxycholate, and dialyzing to remove the detergent. The H-2 antigen-bearing, cell-sized beads, termed pseudocytes (artificial cells), were able to simulate generation of secondary CTL responses with the same specificity as alloantigen-bearing spleen cells. Comparative analyses demonstrated that the size of an antigen-bearing structure, and thus its potential for multivalent interaction, was a critical determinant of effectiveness of antigen recognition, and showed that H-2 antigen was recognized as effectively on cell-sized beads as on allogeneic spleen cells. Generation of a response to antigen on the cell-sized beads was completely dependent on addition of lymphokines to the cultures. Thus, unlike liposomes, H-2 antigen on beads was not available to accessory cells for stimulation of Ia-dependent production of lymphokines by T helper cells. These results, as well as direct observations by microscopy, strongly indicate that antigen is recognized on the surface of the beads. Despite effective stimulation of secondary CTL responses, antigen on beads was completely inactive in stimulating a primary CTL response by naive spleen cells. The results of mixing experiments by using beads and alloantigen-bearing cells or plasma membrane vesicles indicate that the lack of a primary response may result from a requirement for a soluble factor(s) that is not needed for generation of secondary responses. The unique advantages of cell-size supported membranes for studying antigen recognition by T cells are discussed. The beads can be handled and used like antigen-bearing cells in functional assays, while possessing well-defined, readily varied, and easily quantitated composition.
通过简单的透析程序制备了携带I类抗原的新型细胞大小的支撑人工膜,然后用于研究前体细胞毒性T淋巴细胞(CTL)对抗原识别的要求。这些膜是通过将脂质、H-2抗原和C18烷基化的5微米硅胶珠在脱氧胆酸盐中混合,然后透析以去除去污剂制成的。携带H-2抗原的细胞大小的珠子,称为假细胞(人工细胞),能够模拟二级CTL反应的产生,其特异性与携带同种异体抗原的脾细胞相同。比较分析表明,携带抗原结构的大小及其多价相互作用的潜力是抗原识别有效性的关键决定因素,并表明H-2抗原在细胞大小的珠子上与在同种异体脾细胞上一样能被有效识别。对细胞大小珠子上抗原的反应的产生完全依赖于向培养物中添加淋巴因子。因此,与脂质体不同,珠子上的H-2抗原不能被辅助细胞用于刺激T辅助细胞产生依赖Ia的淋巴因子。这些结果以及显微镜下的直接观察强烈表明,抗原是在珠子表面被识别的。尽管二级CTL反应受到有效刺激,但珠子上的抗原在刺激幼稚脾细胞的初级CTL反应中完全无活性。使用珠子与携带同种异体抗原的细胞或质膜囊泡进行混合实验的结果表明,缺乏初级反应可能是由于对二级反应产生不需要的可溶性因子的需求。讨论了细胞大小支撑膜在研究T细胞抗原识别方面的独特优势。这些珠子在功能测定中可以像携带抗原的细胞一样处理和使用,同时具有明确、易于变化且易于定量的组成。