Article

Arachidonic acid metabolism regulates Escherichia coli penetration of the blood-brain barrier.

Division of Pediatric Infectious Diseases, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Infection and immunity (impact factor: 4.21). 10/2010; 78(10):4302-10. DOI:10.1128/IAI.00624-10 pp.4302-10
Source: PubMed

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.

0 0
 · 
0 Bookmarks
 · 
40 Views

Keywords

arachidonic acid
 
arachidonic acid metabolism regulates E. coli penetration
 
blood-brain barrier
 
cysteinyl leukotrienes
 
E. coli invasion
 
E. coli K1 invasion
 
E. coli penetration
 
elucidate
 
Escherichia coli K1 meningitis
 
first direct evidence
 
host 5-lipoxygenase
 
host cytosolic phospholipase A(2)α
 
human brain microvascular endothelial cells
 
incompletely
 
lipoxygenase products
 
membrane phospholipids
 
metabolic products
 
PKCα
 
protein kinase C alpha
 
underlying mechanisms
 

Longkun Zhu