Wu Jun, Yang De-mao, Yang Tai-cheng, Wang Xiao-huai, Wang Jie, Chen Zheng-liang, Fu Ning
Institute of Tumor Molecular Biology, General Hospital of Guangzhou Command, Guangzhou 510010, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2004 Sep;20(5):540-3.
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).
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.
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.
The differentiation of PBMCs towards DCs by CI may be modulated by Ca (2+)/calmodulin and multiple signal transduction pathways downstream.
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。
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。
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。
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。