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Arachidonic Acid Metabolism Regulates Escherichia coli Penetration of the Blood-Brain Barrier

机译:花生四烯酸代谢调节大肠杆菌渗透的血脑屏障。

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Escherichia coli K1 meningitis occurs following penetration of the blood-brain barrier, but the underlying mechanisms involved in E. coli penetration of the blood-brain barrier remain incompletely understood. We have previously shown that host cytosolic phospholipase A2α (cPLA2α) contributes to E. coli invasion of human brain microvascular endothelial cells (HBMEC), which constitute the blood-brain barrier, but the underlying mechanisms remain unclear. cPLA2α selectively liberates arachidonic acid from membrane phospholipids. Here, we provide the first direct evidence that host 5-lipoxygenase and lipoxygenase products of arachidonic acid, cysteinyl leukotrienes (LTs), contribute to E. coli K1 invasion of HBMEC and penetration into the brain, and their contributions involve protein kinase C alpha (PKCα). These findings demonstrate that arachidonic acid metabolism regulates E. coli penetration of the blood-brain barrier, and studies are needed to further elucidate the mechanisms involved with metabolic products of arachidonic acid for their contribution to E. coli invasion of the blood-brain barrier.
机译:大肠杆菌K1脑膜炎是在血脑屏障穿透后发生的,但大肠杆菌对血脑屏障穿透的潜在机制仍未完全了解。先前我们已经表明,宿主细胞溶质磷脂酶A2α(cPLA2α)有助于大肠杆菌入侵人脑微血管内皮细胞(HBMEC),后者构成血脑屏障,但其潜在机制仍不清楚。 cPLA2α从膜磷脂中选择性释放花生四烯酸。在这里,我们提供了第一个直接证据,证明宿主的花生四烯酸,半胱氨酰白三烯(LTs)的5-脂氧合酶和脂氧合酶产物有助于大肠杆菌K1侵袭HBMEC并渗透到脑中,并且它们的贡献涉及蛋白激酶Cα PKCα)。这些发现表明,花生四烯酸的代谢调节了大肠杆菌对血脑屏障的渗透,因此需要进行研究以进一步阐明花生四烯酸的代谢产物对大肠杆菌侵袭血脑屏障的作用。

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