Hansson M, Beran M, Andersson B, Kiessling R
J Immunol. 1982 Jul;129(1):126-32.
This study demonstrates the ability of human NK cells to inhibit in vitro granulopoiesis of autologous and allogeneic BM cells. NK lytic activity and GM-CFC inhibition was present among nonstimulated lymphocytes from healthy donors and could be increased by treatment of PBL with IFN. Both the cytotoxic NK cells and the GM-CFC inhibitory cells could be enriched for among nonadherent, low-density cells. High-density cells were not cytotoxic, only inhibitory to a small extent, and could become neither cytotoxic nor more inhibitory after IFN treatment. In contrast, low-density cells showed an increased cytotoxic and GM-CFC inhibitory capacity after IFN treatment. The NK mediated GM-CFC inhibition was dependent on cell contact with BM cells, increased with longer preincubation times, and was most efficient against 7-day GM-CFC as compared with 14 day GM-CFC progenitors. In conclusion, these data provide new information about the human NK cell as a potent inhibitor of in vitro granulopoiesis and also as a possible regulator of hematopoiesis in vivo.
本研究证明了人类自然杀伤(NK)细胞在体外抑制自体和异体骨髓细胞粒细胞生成的能力。健康供体的未刺激淋巴细胞中存在NK裂解活性和粒细胞-巨噬细胞集落形成细胞(GM-CFC)抑制作用,且用干扰素(IFN)处理外周血淋巴细胞(PBL)可增强这种作用。细胞毒性NK细胞和GM-CFC抑制细胞均可在非贴壁、低密度细胞中富集。高密度细胞无细胞毒性,仅在小程度上有抑制作用,且在IFN处理后既不会产生细胞毒性也不会增强抑制作用。相反,低密度细胞在IFN处理后细胞毒性和GM-CFC抑制能力增强。NK介导的GM-CFC抑制作用依赖于细胞与骨髓细胞的接触,随着预孵育时间延长而增强,与14天的GM-CFC祖细胞相比,对7天的GM-CFC最为有效。总之,这些数据提供了关于人类NK细胞作为体外粒细胞生成的有效抑制剂以及体内造血可能调节因子的新信息。