Herrmann F, Schmidt R E, Ritz J, Griffin J D
Blood. 1987 Jan;69(1):246-54.
We studied the effects of a series of well-characterized clones of human natural killer (NK) cells on the proliferation of highly purified normal marrow hematopoietic progenitor cells. Individual NK clones suppressed granulocyte, monocyte, erythroid, or mixed colony formation in a heterogeneous but clonally stable manner. Inhibition of colony growth required a period of close cell contact between NK cell and progenitor cell with maximum inhibition occurring after 8 to 18 hours of preincubation time. The mechanism of killing was at least partially humoral, however, as cell-free supernatants generated by NK clones "activated" by contact with a target cell also inhibited progenitor cell growth. One of the possible humoral mediators was identified as gamma-interferon by studies with specific neutralizing monoclonal antibodies. These results show that clonal NK lines can be further activated by coming in contact with hematopoietic progenitor cells, resulting in substantial inhibition of colony formation in vitro.
我们研究了一系列特性明确的人类自然杀伤(NK)细胞克隆对高度纯化的正常骨髓造血祖细胞增殖的影响。单个NK克隆以异质性但克隆稳定的方式抑制粒细胞、单核细胞、红系或混合集落的形成。集落生长的抑制需要NK细胞与祖细胞之间有一段紧密的细胞接触期,预孵育8至18小时后抑制作用最大。然而,杀伤机制至少部分是体液性的,因为与靶细胞接触而“活化”的NK克隆产生的无细胞上清液也抑制祖细胞生长。通过使用特异性中和单克隆抗体的研究,确定其中一种可能的体液介质为γ干扰素。这些结果表明,克隆性NK系通过与造血祖细胞接触可进一步活化,从而在体外显著抑制集落形成。