Kawasaki A, Shinkai Y, Yagita H, Okumura K
Department of Immunology, Juntendo University School of Medicine, Tokyo, Japan.
Eur J Immunol. 1992 May;22(5):1215-9. doi: 10.1002/eji.1830220516.
We have previously detected perforin expression in a subpopulation of asialo GM1+ natural killer (NK) cells and CD8+ T lymphocytes in murine spleen cells by immunocytochemical staining with an anti-perforin monoclonal antibody. In the present study, more detailed analyses of perforin expression in murine cytotoxic lymphocyte subpopulations were performed. The expression of perforin in asialo GM1+ spleen cells was predominantly confined to the NK1.1+ subset, where all NK activity also resided. Perforin expression was also studied on alloreactive cytotoxic T lymphocyte (CTL) induced in vivo. The cells expressing perforin in peritoneal exudate lymphocytes predominantly resided in the CD8+ T cell subpopulation co-expressing asialo GM1 where an allospecific CTL activity also resided. Furthermore, the percentage of perforin-positive cells in this population was greatly reduced after stimulation with anti-CD3 or anti-T cell receptors antibodies, which induce serine esterase release from the cytoplasmic granules. These findings highly suggest that perforin is involved in in vivo NK cell- and CTL-mediated cytolysis.
我们之前通过用抗穿孔素单克隆抗体进行免疫细胞化学染色,在小鼠脾细胞中的一群去唾液酸GM1+自然杀伤(NK)细胞和CD8+ T淋巴细胞中检测到了穿孔素的表达。在本研究中,我们对小鼠细胞毒性淋巴细胞亚群中穿孔素的表达进行了更详细的分析。去唾液酸GM1+脾细胞中穿孔素的表达主要局限于NK1.1+亚群,所有NK活性也存在于该亚群中。我们还研究了体内诱导的同种异体反应性细胞毒性T淋巴细胞(CTL)中穿孔素的表达。腹膜渗出淋巴细胞中表达穿孔素的细胞主要存在于共表达去唾液酸GM1的CD8+ T细胞亚群中,同种特异性CTL活性也存在于该亚群中。此外,在用抗CD3或抗T细胞受体抗体刺激后,该群体中穿孔素阳性细胞的百分比大大降低,这些抗体可诱导丝氨酸酯酶从细胞质颗粒中释放。这些发现强烈表明穿孔素参与了体内NK细胞和CTL介导的细胞溶解作用。