Delfino D V, Salcedo M, Marco B D, Ayroldi E, Nocentini G, Bruscoli S, Brunetti L, Ljunggren H G, Riccardi C
Department of Clinical and Experimental Medicine, Section of Pharmacology, University of Perugia, Italy.
Cell Growth Differ. 2001 Jan;12(1):51-60.
To investigate the role of MHC class I on in vitro differentiation of natural killer (NK) cells, a CD44low/-CD2-classlow population was isolated from mouse bone marrow. This population, which lacked expression of NK-1.1, Ly49A, Ly49C/I, and Ly49G, generated populations of NK-1.1+ NK cells expressing Ly49A, Ly49C/I, or Ly49G when cocultured for 13 days with syngeneic supportive stromal cells in the presence of interleukin 2. Ly49A and Ly49C/I were absent on the progeny of progenitors tested after 7 days of culture but were expressed as a late event together with low-level expression of NK-1.1, from day 8 of culture. The addition of anti-H-2b monoclonal antibody to cultures at day 0 inhibited proliferation of progenitors supported by either syngeneic, allogeneic, or H-2b-deficient stromal cells, thus suggesting that the effect was not exerted on stromal cells. Additional analyses demonstrated that class Ilow progenitors generated class I+ cells on which the anti-H-2b monoclonal antibody exerted its inhibitory effect.
为了研究MHC I类分子在自然杀伤(NK)细胞体外分化中的作用,从小鼠骨髓中分离出CD44low/-CD2-classlow细胞群。该细胞群缺乏NK-1.1、Ly49A、Ly49C/I和Ly49G的表达,在白细胞介素2存在的情况下,与同基因支持性基质细胞共培养13天时,可产生表达Ly49A、Ly49C/I或Ly49G的NK-1.1+ NK细胞群。培养7天后检测的祖细胞后代中不存在Ly49A和Ly49C/I,但从培养第8天起,它们与低水平表达的NK-1.1一起作为晚期事件表达。在第0天向培养物中添加抗H-2b单克隆抗体可抑制由同基因、异基因或H-2b缺陷型基质细胞支持的祖细胞增殖,因此表明该效应不是作用于基质细胞。进一步分析表明,class Ilow祖细胞产生class I+细胞,抗H-2b单克隆抗体对其发挥抑制作用。