Endothelial MAPKs Direct ICAM-1 Signaling to Divergent Inflammatory Functions

J Immunol. 2017 May 15;198(10):4074-4085. doi: 10.4049/jimmunol.1600823. Epub 2017 Apr 3.

Abstract

Lymphocyte transendothelial migration (TEM) is critically dependent on intraendothelial signaling triggered by adhesion to ICAM-1. Here we show that endothelial MAPKs ERK, p38, and JNK mediate diapedesis-related and diapedesis-unrelated functions of ICAM-1 in cerebral and dermal microvascular endothelial cells (MVECs). All three MAPKs were activated by ICAM-1 engagement, either through lymphocyte adhesion or Ab-mediated clustering. MAPKs were involved in ICAM-1-dependent expression of TNF-α in cerebral and dermal MVECs, and CXCL8, CCL3, CCL4, VCAM-1, and cyclooxygenase 2 (COX-2) in cerebral MVECs. Endothelial JNK and to a much lesser degree p38 were the principal MAPKs involved in facilitating diapedesis of CD4+ lymphocytes across both types of MVECs, whereas ERK was additionally required for TEM across dermal MVECs. JNK activity was critical for ICAM-1-induced F-actin rearrangements. Furthermore, activation of endothelial ICAM-1/JNK led to phosphorylation of paxillin, its association with VE-cadherin, and internalization of the latter. Importantly ICAM-1-induced phosphorylation of paxillin was required for lymphocyte TEM and converged functionally with VE-cadherin phosphorylation. Taken together we conclude that during lymphocyte TEM, ICAM-1 signaling diverges into pathways regulating lymphocyte diapedesis, and other pathways modulating gene expression thereby contributing to the long-term inflammatory response of the endothelium.

MeSH terms

  • Actins / metabolism
  • Brain / blood supply
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / physiology
  • Cell Movement
  • Cells, Cultured
  • Chemokine CCL3 / genetics
  • Chemokine CCL3 / immunology
  • Chemokine CCL4 / genetics
  • Chemokine CCL4 / immunology
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Dermis / blood supply
  • Endothelial Cells / immunology
  • Endothelial Cells / metabolism*
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / metabolism
  • Enzyme Activation
  • Humans
  • Inflammation / immunology
  • Inflammation / metabolism*
  • Intercellular Adhesion Molecule-1 / metabolism*
  • Interleukin-8 / genetics
  • Interleukin-8 / immunology
  • MAP Kinase Signaling System
  • Microvessels
  • Mitogen-Activated Protein Kinases / metabolism*
  • Paxillin / metabolism
  • Phosphorylation
  • Signal Transduction*
  • Transendothelial and Transepithelial Migration*
  • Tumor Necrosis Factor-alpha / metabolism
  • Vascular Cell Adhesion Molecule-1 / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Actins
  • CCL3 protein, human
  • CCL4 protein, human
  • CXCL8 protein, human
  • Chemokine CCL3
  • Chemokine CCL4
  • ICAM1 protein, human
  • Interleukin-8
  • PXN protein, human
  • Paxillin
  • Tumor Necrosis Factor-alpha
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases