D'Adamio L, Cannarile L, Migliorati G, Riccardi C
Institute of Pharmacology, School of Medicine, University of Perugia, Italy.
J Biol Regul Homeost Agents. 1988 Apr-Jun;2(2):71-6.
The development of natural killer (NK) cells from undifferentiated bone marrow (BM) precursors of low-NK-reactive SJL/J mice was studied. Results indicate that BM cells of untreated mice are not able to generate NK effector cells in cultures supplemented with recombinant interleukin-2 (IL-2). On the other hand in the presence of IL-2, NK cells are generated in cultures of BM from mice pretreated with 5-fluorouracil (5-FU, 150 mg/kg iv 4 days before harvesting), a treatment which has been shown to eliminate more differentiated but spare less differentiated BM precursors. The 5-FU resistant BM progenitor is asialoGM1-, Thy.1+, Lyt.1- and Lyt.2-. The cells generated by culturing with IL-2 are asialoGM1+, Thy.1+, Lyt.5+, Lyt.1-, Lyt.2- and lyse only NK-susceptible targets. Generation of NK cells is blocked by addition of anti-IL-2 receptor (IL-2/r) antibodies. These studies demonstrate that it is possible to generate NK effectors from SJL/J BM cells by in vitro culturing with IL-2.
对低自然杀伤(NK)反应性SJL/J小鼠未分化骨髓(BM)前体细胞向NK细胞的发育进行了研究。结果表明,在添加重组白细胞介素-2(IL-2)的培养物中,未处理小鼠的BM细胞无法产生NK效应细胞。另一方面,在IL-2存在的情况下,用5-氟尿嘧啶(5-FU,收获前4天静脉注射150 mg/kg)预处理的小鼠的BM培养物中会产生NK细胞,已证明这种处理可消除更多分化的但保留较少分化的BM前体细胞。5-FU抗性BM祖细胞无唾液酸GM1-、Thy.1+、Lyt.1-和Lyt.2-。用IL-2培养产生的细胞无唾液酸GM1+、Thy.1+、Lyt.5+、Lyt.1-、Lyt.2-,且仅裂解NK敏感靶细胞。添加抗IL-2受体(IL-2/r)抗体可阻断NK细胞的产生。这些研究表明,通过用IL-2进行体外培养,有可能从SJL/J BM细胞产生NK效应细胞。