骨髓中增殖的单核吞噬细胞长期培养的特点。

J W van der Meer, J S van de Gevel, R van Furth
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引用次数: 0

摘要

研究了小鼠骨髓单核吞噬细胞在胚胎成纤维细胞条件培养基中长期培养的特点,以确定这些细胞的发育阶段和活化状态。采用两种液体培养系统:在细胞水平上研究细胞形态、细胞化学和功能特征,将细胞贴壁培养在玻璃表面;对于需要悬浮细胞的实验(复制实验、运动、细胞内杀伤和细胞毒性研究),使用聚四氟乙烯培养系统。在这些培养物中可以很容易地识别出单核吞噬细胞的三个发育阶段:单核细胞、单核细胞和巨噬细胞。在玻璃表面的培养中,这些细胞在与粒细胞菌落分离的菌落中生长。当孵育超过7-9天,粒细胞死亡,留下纯单核吞噬细胞培养物。原代培养可维持3-4周,其中单核细胞、单核细胞和部分巨噬细胞增殖。计算表明,第0天存在的一个单核细胞在第14天产生了超过7 × 10(3)个单核吞噬细胞的后代;在此之后,尽管添加了新鲜培养基,但增殖速度下降。在聚四氟乙烯上培养的细胞定期复制,可以在近200天的时间内保持增殖。培养的细胞具有典型的单核吞噬细胞的特征,通过光镜判断,α -丁酸萘酯酶活性,溶菌酶活性,Fc和C3受体的存在,以及内吞,杀微生物和细胞毒性活性。5′核苷酸酶活性、红细胞通过c3受体摄取、运动和抗体依赖的细胞毒性表明,培养的骨髓单核吞噬细胞比驻留的巨噬细胞更活跃,与巯基乙酸盐诱导的巨噬细胞一样活跃,甚至更活跃。综上所述,骨髓液体培养中的单核吞噬细胞在发育阶段和激活状态方面具有异质性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics of long-term cultures of proliferating, mononuclear phagocytes from bone marrow.

The characteristics of murine bone marrow mononuclear phagocytes in long-term cultures with embryonic fibroblast-conditioned medium were studied to determine the stage of development and state of activation of these cells. Two liquid culture systems were used: for studies on the morphology, cytochemistry, and functional characteristics at the cellular level, the cells were cultured adherent to a glass surface; and for experiments where the cells were needed in suspension (replating experiments, and studies on locomotion, intracellular killing, and cytotoxicity) use was made of Teflon culture systems. Three developmental stages of mononuclear phagocytes could be recognized easily in these cultures: monoblasts, promonocytes, and macrophages. In cultures on a glass surface, these cells grow in colonies separate from granulocytic colonies. When incubation is prolonged beyond 7-9 days, the granulocytes die, leaving pure mononuclear phagocyte cultures. Primary cultures, in which monoblasts, promonocytes, and some macrophages proliferate, can be maintained for 3-4 weeks. Calculation showed that one monoblast present on day 0 gives rise to a progeny of more than 7 X 10(3) mononuclear phagocytes by day 14; after that, the rate of proliferation declines despite the addition of fresh media. Regular replating of the cells cultured on Teflon made it possible to maintain proliferation over a period of almost 200 days. The cells in culture have the typical characteristics of mononuclear phagocytes, as judged by light microscopy, alpha-naphthyl butyrate esterase activity, lysozyme activity, presence of receptors for Fc and C3, and endocytic, microbicidal, and cytotoxic activity. The 5'nucleotidase activity, ingestion of erythrocytes via C3-receptor, locomotion, and antibody-dependent cytotoxicity indicate that the cultured bone marrow mononuclear phagocytes are more active than resident macrophages, and as active as or even more active than thioglycollate-induced macrophages. In conclusion, the population of mononuclear phagocytes in the liquid cultures of bone marrow is heterogenous with respect to developmental stage and state of activation.

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