Effects of donor age on proteasome activity and senescence in trabecular meshwork cells.

Published

Journal Article

The mechanisms involved in the progressive malfunction of the trabecular meshwork (TM) in glaucoma are not yet understood. To study age-related changes in human TM cells, we isolated primary TM cell cultures from young (ages 9, 14, and 25) and old (ages 66, 70, and 73) donors, and compared levels of oxidized proteins, autofluorescence, proteasome function, and markers for cellular senescence. TM cells from old donors showed a 3-fold increase in oxidized proteins and a 7.5-fold decrease of proteasome activity. Loss of proteasome function was not associated with decreased proteasome content but with partial replacement of the proteolytic subunit PSMB5 with the inducible subunit LMP7. Cells from old donors also demonstrated features characteristic of cellular senescence associated with phosphorylation of p38MAPK but only a modest increase in p53. These data suggest that age-related proteasome inhibition and cellular senescence could contribute to the pathophysiological alterations of the TM in glaucoma.

Full Text

Duke Authors

Cited Authors

  • Caballero, M; Liton, PB; Challa, P; Epstein, DL; Gonzalez, P

Published Date

  • October 22, 2004

Published In

Volume / Issue

  • 323 / 3

Start / End Page

  • 1048 - 1054

PubMed ID

  • 15381105

Pubmed Central ID

  • 15381105

International Standard Serial Number (ISSN)

  • 0006-291X

Digital Object Identifier (DOI)

  • 10.1016/j.bbrc.2004.08.195

Language

  • eng

Conference Location

  • United States