细胞因子对早期b淋巴生成的调节作用。

Blood cells Pub Date : 1994-01-01
F Hirayama, M Ogawa
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引用次数: 0

摘要

利用两步甲基纤维素培养系统,可以从成年小鼠骨髓细胞中培养出能够表达b细胞和髓系的淋巴造血祖细胞。在该系统中,表达髓系的原代菌落被置于继代培养中形成b淋巴细胞菌落。我们观察到,基于钢铁因子(SLF)的两种因子的组合,如SLF +白细胞介素(IL)-6、SLF +粒细胞集落刺激因子(G-CSF)和SLF + IL-11,支持b细胞祖细胞从淋巴造血祖细胞分化和增殖。令人惊讶的是,无论是单独还是与其他因素联合,IL-3都不能支持B淋巴生成。此外,当添加到允许培养条件时,IL-3和IL-1分别抑制原代菌落的b细胞潜能。在体外系统中观察到的IL-3和IL-1的抑制作用可能对造血干细胞体外扩增的细胞因子组合的选择具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytokine regulation of early B-lymphopoiesis assessed in culture.

Lymphohemopoietic progenitors that are capable of expressing B-cell and myeloid lineages may be cultured from bone marrow cells of adult mice by using a two-step methylcellulose culture system. In this system, the primary colonies expressing myeloid lineages are plated in secondary culture for B-lymphoid colony formation. We have observed that combinations of two factors based on steel factor (SLF), such as SLF plus interleukin (IL)-6, SLF plus granulocyte colony-stimulating factor (G-CSF), and SLF plus IL-11 support the differentiation and proliferation of B-cell progenitors from the lymphohemopoietic progenitors. Surprisingly, IL-3 failed to support B lymphopoiesis either alone or in combination with other factors. In addition, when added to permissive culture conditions, IL-3 and IL-1 independently inhibited the B-cell potential of the primary colonies. The inhibitory effects of IL-3 and IL-1 observed in this in vitro system may be significant in the selection of cytokine combinations for in vitro expansion of hemopoietic stem cells.

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