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淋巴因子诱导的巨噬细胞聚集:镁离子参与的研究

Lymphokine-induced macrophage aggregation: studies on the involvement of Mg2+.

作者信息

Badenoch-Jones P

出版信息

Immunopharmacology. 1982 Apr;4(2):115-23. doi: 10.1016/0162-3109(82)90014-5.

Abstract

The divalent cation requirements of lymphokine (LK)-induced macrophage aggregation have been investigated using a quantitative assay. It has been shown that LK-induced aggregation is dependent on exogenous Mg2+ but not Ca2+. By contrast, aggregation induced ty the ionophore A23187 is dependent on exogenous Ca2+ and Mg2+. Furthermore, exogenous Mg2+, at 0.5-5.0 mmol, both mimics the aggregation effects of LK and stimulates LK-induced aggregation. Additionally, both chlorpromazine and trifluoperazine inhibited aggregation indiced by LK, A23187, and exogenous Mg2+. Similarly, prostaglandin (PG)E2 inhibited, and indomethacin (10 micro M) stimulated, aggregation induced by these three agents. These results are discussed in the context of the mode of action of macrophage aggregating factor (MAgF).

摘要

利用定量测定法研究了淋巴因子(LK)诱导的巨噬细胞聚集对二价阳离子的需求。结果表明,LK诱导的聚集依赖于外源性Mg2+而非Ca2+。相比之下,离子载体A23187诱导的聚集依赖于外源性Ca2+和Mg2+。此外,0.5 - 5.0 mmol的外源性Mg2+既能模拟LK的聚集效应,又能刺激LK诱导的聚集。另外,氯丙嗪和三氟拉嗪均抑制LK、A23187和外源性Mg2+诱导的聚集。同样,前列腺素(PG)E2抑制这三种试剂诱导的聚集,而吲哚美辛(10 μM)则刺激这种聚集。将在巨噬细胞聚集因子(MAgF)的作用模式背景下讨论这些结果。

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