Brunet J F, Denizot F, Suzan M, Haas W, Mencia-Huerta J M, Berke G, Luciani M F, Golstein P
J Immunol. 1987 Jun 15;138(12):4102-5.
We and other investigators previously reported the cloning of CTLA-1 (or CCP-1) and CTLA-3 (or H Factor) serine esterase-related transcripts preferentially expressed in cytolytic T lymphocytes. We extended the survey of the tissue specificity of these molecules. Two main sets of results were obtained. First, both CTLA-1 and CTLA-3 transcripts could be found in the various cytolytic T cells tested, although in widely different amounts, and in some cases just at the threshold of detection. Secondly, these transcripts were not found in most of the other cells tested, including in some natural cytotoxic cells and in activated cytotoxic macrophages; however, they could be detected in mast cells for CTLA-1 and in some noncytotoxic lymphocytes for CTLA-3. Thus, the CTLA-1 and CTLA-3 serine esterase products are most probably not required for macrophage or natural cytotoxicity; their presence cannot be taken as characteristic of cytotoxic T cells; and a discussion about their relevance to T cell-mediated cytotoxicity should take into account their widely different amounts from one cytotoxic T cell to another.
我们和其他研究人员之前报道了CTLA-1(或CCP-1)和CTLA-3(或H因子)丝氨酸酯酶相关转录本的克隆,这些转录本在细胞毒性T淋巴细胞中优先表达。我们扩展了对这些分子组织特异性的研究。获得了两组主要结果。首先,在测试的各种细胞毒性T细胞中都能发现CTLA-1和CTLA-3转录本,尽管数量差异很大,在某些情况下仅处于检测阈值。其次,在测试的大多数其他细胞中未发现这些转录本,包括一些自然杀伤细胞和活化的细胞毒性巨噬细胞;然而,CTLA-1的转录本可在肥大细胞中检测到,CTLA-3的转录本可在一些非细胞毒性淋巴细胞中检测到。因此,巨噬细胞或自然杀伤作用很可能不需要CTLA-1和CTLA-3丝氨酸酯酶产物;它们的存在不能被视为细胞毒性T细胞的特征;关于它们与T细胞介导的细胞毒性相关性的讨论应考虑到它们在不同细胞毒性T细胞中的含量差异很大。