Senescence in cultured trabecular meshwork cells

Br J Ophthalmol. 2007 Jun;91(6):808-11. doi: 10.1136/bjo.2006.108423. Epub 2007 Jan 10.

Abstract

Background: It has been suggested that replicative senescence might be involved in the pathophysiology of age-related diseases.

Aim: To study the process of senescence in trabecular meshwork (TM) cells.

Methods: Porcine TM tissues were obtained and placed in primary cultures with Dulbecco's modified Eagle's medium/Ham's F-12 medium. After 2-3 weeks, migrated and proliferated TM cells were trypsinised and cultured in serial passages, and identified with fluorescein-labelled low-density lipoprotein (DiI-Ac-LDL), a marker of TM cells. Staining for senescence-related beta-galactosidase activity was performed at population doubling level (PDL) 2, 8 and 16 at pH 6. Terminal restriction fragment (TRF) length was examined by Southern blot analysis using a (32)P-labelled telomere-specific sequence (TTAGGG)(3) at each PDL.

Results: DiI-Ac-LDL staining revealed that most (nearly 100%) of the cells in the culture were TM cells, which were flattened in shape and positive for senescence-related beta-galactosidase staining at PDL 16. Reduction of TRF length as a function of population doubling was also shown.

Conclusions: TM cells exhibited characteristics of senescence at PDL 16 in vitro. The results demonstrated that cellular senescence may be related to the pathophysiology of primary open-angle glaucoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Culture Techniques / methods
  • Cell Proliferation
  • Cell Shape
  • Cellular Senescence*
  • Lipoproteins, LDL / metabolism
  • Polymorphism, Restriction Fragment Length
  • Swine
  • Telomere
  • Tissue Culture Techniques
  • Trabecular Meshwork / cytology*
  • Trabecular Meshwork / metabolism
  • Up-Regulation
  • beta-Galactosidase / metabolism

Substances

  • Lipoproteins, LDL
  • beta-Galactosidase