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[钙离子载体诱导人外周血单核细胞向树突状细胞分化过程中的信号转导]

[Signal transduction in the differentiation of human peripheral blood mononucleocytes towards dendritic cells induced by calcium ionophore].

作者信息

Wu Jun, Yang De-mao, Yang Tai-cheng, Wang Xiao-huai, Wang Jie, Chen Zheng-liang, Fu Ning

机构信息

Institute of Tumor Molecular Biology, General Hospital of Guangzhou Command, Guangzhou 510010, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2004 Sep;20(5):540-3.

Abstract

AIM

To explore the intracellular signal transduction pathway in the differentiation of human peripheral blood mononucleocytes (PBMCs) towards dendritic cells (DCs) induced by calcium ionophore (CI).

METHODS

PBMCs isolated from a healthy donor were cultured with A23187 plus rhGM-CSF, 100 microg/L each. In some experiments, PBMCs were cultured for 30 minutes with W-7 (10 micromol/L), CsA(0.5 mg/L) or KT5926(1 micromol/L) before addition of rhGM-CSF and A23187. After culture for 40 hours, morphological change of the cells were observed under phase contrast microscope; surface markers on treated PBMCs were analyzed by flow cytometry; the proliferation of allogeneic human T cells stimulated by the treated PBMCs was detected by MTT colorimetry.

RESULTS

PBMCs of the healthy donor cocultured with rhGM-CSF plus CI for 40 hours had the typical morphology of DCs, with decreased CD14 expression, and increased CD83, CD80 and CD86 expressions. The proliferation of allogeneic T cells stimulated by PBMCs treated with A23187 plus rhGM-CSF was strengthened. But the morphological changes, surface marker expressions and the ability to enhancing proliferation of allogeneic T cells were inhibited to different degrees by W-7, CsA or KT5926.

CONCLUSION

The differentiation of PBMCs towards DCs by CI may be modulated by Ca (2+)/calmodulin and multiple signal transduction pathways downstream.

摘要

目的

探讨钙离子载体(CI)诱导人外周血单个核细胞(PBMCs)向树突状细胞(DCs)分化的细胞内信号转导途径。

方法

从健康供体分离的PBMCs与A23187加重组人粒细胞-巨噬细胞集落刺激因子(rhGM-CSF)(各100μg/L)共同培养。在一些实验中,PBMCs在加入rhGM-CSF和A23187之前,先用W-7(10μmol/L)、环孢素A(CsA)(0.5mg/L)或KT5926(1μmol/L)培养30分钟。培养40小时后,在相差显微镜下观察细胞形态变化;用流式细胞术分析处理后的PBMCs表面标志物;用MTT比色法检测处理后的PBMCs刺激的同种异体人T细胞的增殖。

结果

健康供体的PBMCs与rhGM-CSF加CI共同培养40小时后具有典型的DCs形态,CD14表达降低,CD83、CD80和CD86表达增加。A23187加rhGM-CSF处理的PBMCs刺激的同种异体T细胞增殖增强。但W-7、CsA或KT5926在不同程度上抑制了细胞形态变化、表面标志物表达及增强同种异体T细胞增殖的能力。

结论

CI诱导PBMCs向DCs的分化可能受Ca(2+)/钙调蛋白及下游多条信号转导途径调控。

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