Advanced glycation end products-related modulation of cathepsin L and NF-κB signalling effectors in retinal pigment epithelium lead to augmented response to TNFα

Sharif, Umar and Mahmud, Nur Musfirah and Kay, Paul and Yang, Yit C. and Harding, Simon Peter and Grierson, Ian and Kamalden, Tengku Ain and Jackson, Malcolm J. and Paraoan, Luminita (2018) Advanced glycation end products-related modulation of cathepsin L and NF-κB signalling effectors in retinal pigment epithelium lead to augmented response to TNFα. Journal of Cellular and Molecular Medicine, 23 (1). pp. 405-416. ISSN 1582-1838, DOI https://doi.org/10.1111/jcmm.13944.

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Official URL: https://doi.org/10.1111/jcmm.13944

Abstract

The retinal pigment epithelium (RPE) plays a central role in neuroretinal homoeostasis throughout life. Altered proteolysis and inflammatory processes involving RPE contribute to the pathophysiology of age-related macular degeneration (AMD), but the link between these remains elusive. We report for the first time the effect of advanced glycation end products (AGE)—known to accumulate on the ageing RPE's underlying Bruch's membrane in situ—on both key lysosomal cathepsins and NF-κB signalling in RPE. Cathepsin L activity and NF-κB effector levels decreased significantly following 2-week AGE exposure. Chemical cathepsin L inhibition also decreased total p65 protein levels, indicating that AGE-related change of NF-κB effectors in RPE cells may be modulated by cathepsin L. However, upon TNFα stimulation, AGE-exposed cells had significantly higher ratio of phospho-p65(Ser536)/total p65 compared to non-AGEd controls, with an even higher fold increase than in the presence of cathepsin L inhibition alone. Increased proportion of active p65 indicates an AGE-related activation of NF-κB signalling in a higher proportion of cells and/or an enhanced response to TNFα. Thus, NF-κB signalling modulation in the AGEd environment, partially regulated via cathepsin L, is employed by RPE cells as a protective (para-inflammatory) mechanism but renders them more responsive to pro-inflammatory stimuli.

Item Type: Article
Funders: The Foundation for Prevention of Blindness, University of Malaya (Research Grant No. RP033‐ 14HTM), The Humane Research Trust UK, The R & D Royal Wolverhampton NHS Trust, Wolverhampton, UK
Uncontrolled Keywords: Age-related macular degeneration; Cathepsin, NF-κB signalling; Inflammation; Proteolysis; Retinal pigment epithelium
Subjects: R Medicine
Divisions: Faculty of Medicine
Depositing User: Ms. Juhaida Abd Rahim
Date Deposited: 15 Jan 2019 01:11
Last Modified: 15 Jan 2019 01:11
URI: http://eprints.um.edu.my/id/eprint/19995

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