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植物血凝素处理的血液单核细胞对粒细胞和巨噬细胞集落刺激因子产生的调节

Regulation of granulocyte and macrophage colony-stimulating factor production by phytohaemagglutinin-treated blood mononuclear cells.

作者信息

Gordon M Y, Gordon-Smith E C

出版信息

Leuk Res. 1982;6(1):71-9. doi: 10.1016/0145-2126(82)90045-5.

Abstract

The colony-stimulating activity (CSA) of medium conditioned by phytohaemagglutinin (PHA)-stimulated blood mononuclear cells was tested using granulocyte-macrophage colony-forming cells (GM-CFC) from normal bone marrow. Low concentrations of the conditioned medium stimulated granulocytic colony-forming cells (CFC) which formed colonies by the seventh day of incubation; higher concentrations stimulated the formation of macrophage colonies which were not seen until the end of the second week in culture. The colony-stimulating activities could not be demonstrated in adherent cell-depleted bone marrow cultures. This dependence of activity on adherent cells was confirmed by incubating different concentrations of conditioned medium with isolated adherent cells and then testing for colony-stimulating activity in cultures of non-adherent bone marrow cells. The activities of conditioned media following exposure to adherent cells corresponded to the results seen when the conditioned medium from PHA-stimulated mononuclear cell cultures was used to stimulate agar cultures of unseparated marrow. The results suggest that PHA-responsive mononuclear cells (probably T lymphocytes) may modulate the regulation of colony-stimulating factor (CSF) production by adherent colony-stimulating cells (CSC).

摘要

使用来自正常骨髓的粒细胞-巨噬细胞集落形成细胞(GM-CFC),检测经植物血凝素(PHA)刺激的血液单核细胞所产生的条件培养基的集落刺激活性(CSA)。低浓度的条件培养基刺激粒细胞集落形成细胞(CFC),这些细胞在培养的第7天形成集落;高浓度则刺激巨噬细胞集落的形成,直到培养的第二周结束才可见到这些集落。在去除贴壁细胞的骨髓培养物中未显示出集落刺激活性。通过将不同浓度的条件培养基与分离的贴壁细胞一起孵育,然后检测非贴壁骨髓细胞培养物中的集落刺激活性,证实了活性对贴壁细胞的这种依赖性。暴露于贴壁细胞后的条件培养基的活性与使用来自PHA刺激的单核细胞培养物的条件培养基刺激未分离骨髓的琼脂培养物时所观察到的结果一致。结果表明,对PHA有反应的单核细胞(可能是T淋巴细胞)可能调节贴壁集落刺激细胞(CSC)产生集落刺激因子(CSF)的调节作用。

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