Involvement of PKCα-MAPK/ERK-phospholipase A(2) pathway in the Escherichia coli invasion of brain microvascular endothelial cells

Neurosci Lett. 2012 Mar 5;511(1):33-7. doi: 10.1016/j.neulet.2012.01.031. Epub 2012 Jan 24.

Abstract

Escherichia coli K1 is the most common Gram-negative organism that causes neonatal meningitis following penetration of the blood-brain barrier. In the present study we demonstrated the involvement of cytosolic (cPLA(2)) and calcium-independent phospholipase A(2) (iPLA(2)) and the contribution of cyclooxygenase-2 products in E. coli invasion of microvascular endothelial cells. The traversal of bacteria did not determine trans-endothelial electrical resistance (TEER) and ZO-1 expression changes and was reduced by PLA(2)s siRNA. cPLA(2) and iPLA(2) enzyme activities and cPLA(2) phosphorylation were stimulated after E. coli incubation and were attenuated by PLA(2), PI3-K, ERK 1/2 inhibitors. Our results demonstrate the role of PKCα/ERK/MAPK signaling pathways in governing the E. coli penetration into the brain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier
  • Brain / blood supply*
  • Cattle
  • Cells, Cultured
  • Cyclooxygenase 2 / metabolism
  • Cytosol / enzymology
  • Endothelial Cells / microbiology*
  • Endothelial Cells / physiology
  • Endothelium, Vascular / microbiology*
  • Endothelium, Vascular / physiology
  • Enzyme Activation
  • Escherichia coli / pathogenicity*
  • MAP Kinase Signaling System*
  • Membrane Proteins / metabolism
  • Microvessels / microbiology
  • Microvessels / physiology
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Phospholipases A2, Calcium-Independent / antagonists & inhibitors
  • Phospholipases A2, Calcium-Independent / genetics
  • Phospholipases A2, Calcium-Independent / metabolism*
  • Phosphorylation
  • Protein Kinase C-alpha / metabolism*
  • RNA Interference

Substances

  • Membrane Proteins
  • Cyclooxygenase 2
  • Protein Kinase C-alpha
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Phospholipases A2, Calcium-Independent