Arachidonic Acid Metabolism Regulates Escherichia coli Penetration of the Blood-Brain Barrier
Arachidonic Acid Metabolism Regulates Escherichia coli Penetration of the Blood-Brain Barrier
ABSTRACT 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 A 2 α (cPLA 2 α) contributes to E. coli invasion of human brain microvascular endothelial cells (HBMEC), which constitute the blood-brain barrier, but the underlying mechanisms remain unclear. cPLA 2 α 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.
- Johns Hopkins Medicine United States
- University of Michigan–Flint United States
- University of Tennessee System United States
- University of Michigan–Ann Arbor United States
- Johns Hopkins University School of Medicine United States
Mice, Knockout, Leukotrienes, Arachidonate 5-Lipoxygenase, Arachidonic Acid, Protein Kinase C-alpha, Group IV Phospholipases A2, Brain, Endothelial Cells, Mice, Blood-Brain Barrier, Escherichia coli, Animals, Humans
Mice, Knockout, Leukotrienes, Arachidonate 5-Lipoxygenase, Arachidonic Acid, Protein Kinase C-alpha, Group IV Phospholipases A2, Brain, Endothelial Cells, Mice, Blood-Brain Barrier, Escherichia coli, Animals, Humans
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