Oya H, Kawamura T, Shimizu T, Bannai M, Kawamura H, Minagawa M, Watanabe H, Hatakeyama K, Abo T
Department of Immunology and First Department of Surgery, Niigata University School of Medicine, Niigata, Japan.
Clin Exp Immunol. 2000 Aug;121(2):384-90. doi: 10.1046/j.1365-2249.2000.01310.x.
When C57Bl/6 mice were exposed to restraint stress for 12 h or 24 h, lymphocytopenia was induced in the liver, spleen, and thymus. We examined which types of lymphocytes were sensitive or resistant to such stress by a immunofluorescence test. T cells of thymic origin were sensitive while NKT and NK cells were resistant. In contrast to the increase in the proportion of NK cells, NK activity of liver lymphocytes against YAC-1 targets decreased at 24 h after stress. On the other hand, their NKT cytotoxicity against syngeneic thymocytes increased in parallel with an increase in their proportion. In perforin -/- B6 mice and B6-gld/gld (Fas ligand-) mice, NK cells were found to mediate cytotoxicity through perforin while NKT cells mediated self-reactive cytotoxicity through Fas ligand. These results suggest that stress increases the proportion of both NK and NKT cells, but that NK cytotoxicity is suppressed while self-reactive NKT cytotoxicity is not, due to a diversity of their functional mechanisms.
当C57Bl/6小鼠暴露于束缚应激12小时或24小时后,肝脏、脾脏和胸腺中会诱导出淋巴细胞减少。我们通过免疫荧光试验检测了哪些类型的淋巴细胞对这种应激敏感或耐受。胸腺来源的T细胞敏感,而NKT细胞和NK细胞耐受。与NK细胞比例增加相反,应激后24小时,肝脏淋巴细胞对YAC-1靶标的NK活性降低。另一方面,它们对同基因胸腺细胞的NKT细胞毒性与其比例增加平行升高。在穿孔素基因敲除的B6小鼠和B6-gld/gld(Fas配体缺陷)小鼠中,发现NK细胞通过穿孔素介导细胞毒性,而NKT细胞通过Fas配体介导自身反应性细胞毒性。这些结果表明,应激会增加NK细胞和NKT细胞的比例,但由于它们功能机制的多样性,NK细胞毒性受到抑制,而自身反应性NKT细胞毒性不受抑制。