首页> 外文期刊>Biological & pharmaceutical bulletin >Manassantin B isolated from Saururus chinensis inhibits cyclooxygenase-2-dependent prostaglandin D_2 generation by blocking Fyn-mediated nuclear factor-kappaB and mitogen activated protein kinase pathways in bone marrow derived-mast cells
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Manassantin B isolated from Saururus chinensis inhibits cyclooxygenase-2-dependent prostaglandin D_2 generation by blocking Fyn-mediated nuclear factor-kappaB and mitogen activated protein kinase pathways in bone marrow derived-mast cells

机译:分离自Saururus chinensis的Manassantin B通过阻断Fyn介导的核肥大细胞中的Fyn介导的核因子-κB和丝裂原活化的蛋白激酶途径来抑制环氧合酶-2依赖性前列腺素D_2的产生

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摘要

The authors investigated the effect of manassantin B (Man B) isolated from Saururus chinensis (S. chinensis) on cyclooxygenase-2 (COX-2)-dependent prostaglandin D_2 (PGD_2) generation in mouse bone marrow derived-mast cells (BMMCs). Man B inhibited the generation of PGD_2 dose-dependently by inhibiting COX-2 expression in immunoglobulin E (IgE)/Ag-stimulated BMMCs. To elucidate the mechanism responsible for the inhibition of COX-2 expression by Man B, the effects of Man B on the activation of nuclear factor-kappaB (NF-κB), a transcription factor essential and mitogen-activated protein kinases (MAPKs) for COX-2 induction, were examined. Man B attenuated the nuclear translocation of NF-κB p65 and its DNA-binding activity by inhibiting inhibitors of kappa Bα (IκBα) degradation and concomitantly suppressing IκB kinase (IKK) phosphorylation. In addition, Man B suppressed phosphorylation of MAPKs including extracellular signal-regulated kinase 1/2 (ERK1/2), c-Jun NH _2-terminal kinase (JNK) and p38. It was also found that Man B suppressed Fyn kinase activation and consequent downstream signaling processes, including those involving Syk, Gab2, and Akt. Taken together, the present results suggest that Man B suppresses COX-2 dependent PGD_2 generation by primarily inhibiting Fyn kinase in FcεRI-mediated mast cells.
机译:作者研究了从中华龙(Saururus chinensis)(S. chinensis)分离出的Manassantin B(Man B)对小鼠骨髓源性肥大细胞(BMMCs)中环氧合酶2(COX-2)依赖性前列腺素D_2(PGD_2)生成的影响。 Man B通过抑制免疫球蛋白E(IgE)/ Ag刺激的BMMC中COX-2的表达来剂量依赖性地抑制PGD_2的产生。为了阐明Man B抑制COX-2表达的机制,Man B对核因子-κB(NF-κB),转录因子必需和有丝分裂原激活的蛋白激酶(MAPKs)活化的作用。检查了COX-2的诱导。 Man B通过抑制KappaBα(IκBα)降解抑制剂并同时抑制IκB激酶(IKK)磷酸化来减弱NF-κBp65的核易位及其DNA结合活性。另外,Man B抑制了MAPK的磷酸化,包括细胞外信号调节激酶1/2(ERK1 / 2),c-Jun NH _2-末端激酶(JNK)和p38。还发现Man B抑制了Fyn激酶的活化以及随后的下游信号传导过程,包括那些涉及Syk,Gab2和Akt的过程。综上所述,本发明结果提示Man B通过主要抑制FcεRI介导的肥大细胞中的Fyn激酶来抑制COX-2依赖性PGD_2的产生。

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