Role of MCP-1 and IL-8 in viral anterior uveitis, and contractility and fibrogenic activity of trabecular meshwork cells

Sci Rep. 2021 Jul 22;11(1):14950. doi: 10.1038/s41598-021-94391-2.

Abstract

The inflammatory chemokines, monocyte chemoattractant protein (MCP)-1 and IL-8, are produced by normal trabecular meshwork cells (TM) and elevated in the aqueous humor of primary open angle glaucoma (POAG) and hypertensive anterior uveitis associated with viral infection. However, their role in TM cells and aqueous humor outflow remains unclear. Here, we explored the possible involvement of MCP-1 and IL-8 in the physiology of TM cells in the context of aqueous outflow, and the viral anterior uveitis. We found that the stimulation of human TM cells with MCP-1 and IL-8 induced significant increase in the formation of actin stress fibers and focal adhesions, myosin light chain phosphorylation, and the contraction of TM cells. MCP-1 and IL-8 also demonstrated elevation of extracellular matrix proteins, and the migration of TM cells. When TM cells were infected with HSV-1 and CMV virus, there was a significant increase in cytoskeletal contraction and Rho-GTPase activation. Viral infection of TM cells revealed significantly increased expression of MCP-1 and IL-8. Taken together, these results indicate that MCP-1 and IL-8 induce TM cell contractibility, fibrogenic activity, and plasticity, which are presumed to increase resistance to aqueous outflow in viral anterior uveitis and POAG.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aqueous Humor / immunology
  • Cell Movement
  • Cells, Cultured
  • Chemokine CCL2 / metabolism*
  • Cytomegalovirus / pathogenicity
  • Extracellular Matrix Proteins / metabolism
  • Eye Infections, Viral / immunology*
  • Eye Infections, Viral / pathology
  • Herpesvirus 1, Human / pathogenicity
  • Humans
  • Interleukin-8 / metabolism*
  • Middle Aged
  • Primary Cell Culture
  • Receptors, CCR2 / metabolism
  • Receptors, Interleukin-8A / metabolism
  • Trabecular Meshwork / cytology*
  • Trabecular Meshwork / immunology
  • Trabecular Meshwork / virology
  • Uveitis, Anterior / immunology
  • Uveitis, Anterior / pathology
  • Uveitis, Anterior / virology*

Substances

  • CCL2 protein, human
  • CCR2 protein, human
  • CXCL8 protein, human
  • Chemokine CCL2
  • Extracellular Matrix Proteins
  • Interleukin-8
  • Receptors, CCR2
  • Receptors, Interleukin-8A