Matera L, Santoli D, Garbarino G, Pegoraro L, Bellone G, Pagliardi G
J Immunol. 1986 Feb 15;136(4):1260-5.
We describe here the modulatory activity of human peripheral blood natural killer (NK) cells on the growth and differentiation of myeloid progenitor cells at different stages of maturation. NK-enriched cell fractions containing 54 to 75% large granular lymphocytes (LGL) and displaying high levels of NK activity significantly inhibited the growth of late (7 day) granulocyte-macrophage colony-forming cells (CFU-GM) from about 50% of normal human bone marrow samples. However, the same fractions strongly enhanced the growth of early (14 day) stem cells from peripheral blood. Enhancing activity on early CFU-GM from blood was greater in highly purified NK cell preparations containing 96% LGL than in NK-depleted T cell preparations from the same donors. Analogous to the results when using the NK-enriched fractions, the NK-purified preparations inhibited late CFU-GM and stimulated the early ones. We conclude from these observations that human LGL have a modulatory effect on myelopoiesis depending on the maturation stage of the progenitor cell.
我们在此描述人外周血自然杀伤(NK)细胞对不同成熟阶段髓系祖细胞生长和分化的调节活性。富含NK细胞的组分含有54%至75%的大颗粒淋巴细胞(LGL),并表现出高水平的NK活性,可显著抑制约50%正常人骨髓样本中晚期(7天)粒-巨噬细胞集落形成细胞(CFU-GM)的生长。然而,相同的组分可强烈增强外周血早期(14天)干细胞的生长。在含有96%LGL的高度纯化NK细胞制剂中,对血液中早期CFU-GM的增强活性比对来自相同供体的NK细胞耗竭的T细胞制剂更强。与使用富含NK细胞的组分时的结果类似,纯化的NK细胞制剂可抑制晚期CFU-GM并刺激早期CFU-GM。我们从这些观察结果得出结论,人LGL对髓系造血具有调节作用,这取决于祖细胞的成熟阶段。