cAMP Modulates Macrophage Development by Suppressing M-CSF-Induced MAPKs Activation

来源 :Cellular & Molecular Immunology | 被引量 : 0次 | 上传用户:huangshuhui1983
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M-CSF is a key cytokine in macrophage development by inducing MAPKs activation,and cAMP can inhibit MAPKs activation induced by inflammatory stimuli. To explore the effects of cAMP on M-CSF-induced MAPKs activation and on macrophage development,the model of bone marrow-derived murine macrophages (BMMs) was used. The effects of cAMP on M-CSF-induced MAPKs activation were analyzed by Western blotting assay,and the effects of cAMP on CD14 and F4/80 expression during macrophage development were examined by FACS analysis. Macrophage morphology showed the successful establishment of the model of macrophage development. Western blotting assay revealed that M-CSF activated ERK,JNK and p38 in both mature and immature macrophages,and cAMP inhibited M-CSF-induced ERK,JNK and p38 activation in a time-dependent manner. FACS analysis revealed that macrophage development was impaired with cAMP pretreatment. In conclusion,cAMP modulates macrophage development by suppressing M-CSF-induced MAPKs activation. M-CSF is a key cytokine in macrophage development by inducing MAPK activation, and cAMP can inhibit MAPKs activation induced by inflammatory stimuli. To explore the effects of cAMP on M-CSF-induced MAPK activation and on macrophage development, the model of bone marrow The effects of cAMP on M-CSF-induced activation of MAPKs by Western blotting assay, and the effects of cAMP on CD14 and F4 / 80 expression during macrophage development were examined by FACS analysis. Macrophage morphology showed the successful establishment of the model of macrophage development. Western blotting assay revealed that M-CSF activated ERK, JNK and p38 in both mature and immature macrophages, and cAMP inhibited M-CSF-induced ERK, JNK and p38 activation in a time-dependent manner. FACS analysis revealed that macrophage development was impaired with cAMP pretreatment. In conclusion, cAMP modulates macrophage development by suppressing M-CSF-induced MAPKs activat ion.
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