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在培养中评估细胞因子对早期B淋巴细胞生成的调节作用。

Cytokine regulation of early B-lymphopoiesis assessed in culture.

作者信息

Hirayama F, Ogawa M

机构信息

Ralph H. Johnson Department of Veterans Affairs Medical Center, Charleston, SC 29401, USA.

出版信息

Blood Cells. 1994;20(2-3):341-6; discussion 346-7.

PMID:7538338
Abstract

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.

摘要

通过使用两步甲基纤维素培养系统,可从成年小鼠的骨髓细胞中培养出能够表达B细胞和髓系谱系的淋巴细胞造血祖细胞。在该系统中,将表达髓系谱系的原代集落接种于二级培养中以形成B淋巴细胞集落。我们观察到,基于钢因子(SLF)的两种因子组合,如SLF加白细胞介素(IL)-6、SLF加粒细胞集落刺激因子(G-CSF)以及SLF加IL-11,可支持淋巴细胞造血祖细胞中B细胞祖细胞的分化和增殖。令人惊讶的是,IL-3无论是单独使用还是与其他因子联合使用,均无法支持B淋巴细胞生成。此外,当添加到允许的培养条件中时,IL-3和IL-1可独立抑制原代集落的B细胞潜能。在该体外系统中观察到的IL-3和IL-1的抑制作用,对于选择用于造血干细胞体外扩增的细胞因子组合可能具有重要意义。

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