Effect of pigmentation intensity of trabecular meshwork cells on mechanisms of micropulse laser trabeculoplasty

Sci Rep. 2022 Jun 22;12(1):10535. doi: 10.1038/s41598-022-14637-5.

Abstract

The intraocular pressure (IOP)-lowering mechanisms of micropulse laser trabeculoplasty (MLT) remain unclear. The present study was performed to investigate the mechanism of action of MLT, and to determine whether the pigmentation intensity of trabecular meshwork (TM) cells is associated with the treatment effects. Primary human TM cells were exposed to melanin granules to artificially introduce different levels of pigmentation. Micropulse (MP) laser irradiation was performed, and interleukin (IL)-1α/β, matrix metalloproteinases (MMPs), tissue inhibitor of metalloproteinases (TIMPs), and extracellular matrix (ECM) protein expression were evaluated by RT-qPCR and immunocytochemistry. IL-1α/β and MMP-1, -3, and -9 mRNA expression were significantly upregulated at 4 and 24 h after MP laser irradiation, respectively, but there were no significant changes in TIMP expression. The extent of these upregulation was greater in cells with strong pigmentation intensity. Protein expressions of fibronectin and collagen I were significantly decreased in cells with strong staining intensity. These results suggested that MP laser irradiation alter the MMP/TIMP ratio and enhance ECM turnover, resulting in increased outflow of aqueous humor. The pigmentation intensity of the TM tissues may affect the treatment efficacy of MLT, because TM cells with strong staining intensity showed a significantly enhanced response to MP laser irradiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Extracellular Matrix Proteins / metabolism
  • Humans
  • Intraocular Pressure
  • Lasers
  • Matrix Metalloproteinases / genetics
  • Matrix Metalloproteinases / metabolism
  • Pigmentation
  • Tissue Inhibitor of Metalloproteinases / genetics
  • Trabecular Meshwork* / metabolism
  • Trabeculectomy*

Substances

  • Extracellular Matrix Proteins
  • Tissue Inhibitor of Metalloproteinases
  • Matrix Metalloproteinases