Arase H, Arase N, Saito T
Division of Molecular Genetics, Chiba University School of Medicine, Japan.
J Exp Med. 1995 Mar 1;181(3):1235-8. doi: 10.1084/jem.181.3.1235.
The expression of Fas ligand on natural killer (NK) cells and Fas-mediated cytotoxicity by NK cells was investigated. Fas ligand mRNA was expressed in freshly isolated NK cells but not in T cells. Furthermore, the Fas ligand was detected on the cell surface of NK cells by staining with soluble Fas molecule. We analyzed the cytolytic activity of NK cells against thymocyte targets from normal and lpr mice, and found that the NK cells killed thymocytes from normal mice but not from lpr mice. On the other hand, splenic T cells did not show any cytotoxicity against either of the thymocyte targets. Similarly, NK cells exhibited cytotoxicity against transfectants expressing Fas antigen but not against parental cells or transfectants expressing a mutant Fas antigen with deleted cytoplasmic region. These results demonstrated that NK cells express Fas ligand and possess the capability of killing target cells expressing Fas antigen on their surface. This finding suggests that NK cells play an important role by eliminating Fas-expressing cells either constitutively or inducibly in peripheral lymphoid organs.
研究了自然杀伤(NK)细胞上Fas配体的表达以及NK细胞介导的Fas细胞毒性。Fas配体mRNA在新鲜分离的NK细胞中表达,但在T细胞中不表达。此外,通过用可溶性Fas分子染色在NK细胞的细胞表面检测到Fas配体。我们分析了NK细胞对来自正常小鼠和lpr小鼠的胸腺细胞靶标的细胞溶解活性,发现NK细胞杀死正常小鼠的胸腺细胞,但不杀死lpr小鼠的胸腺细胞。另一方面,脾T细胞对任何一种胸腺细胞靶标均未显示出任何细胞毒性。同样,NK细胞对表达Fas抗原的转染子具有细胞毒性,但对亲本细胞或表达缺失细胞质区域的突变Fas抗原的转染子没有细胞毒性。这些结果表明,NK细胞表达Fas配体,并具有杀死其表面表达Fas抗原的靶细胞的能力。这一发现表明,NK细胞通过在周围淋巴器官中组成性或诱导性地消除表达Fas的细胞而发挥重要作用。