PPARβ/δ selectively regulates phenotypic features of age-related macular degeneration

Mayur Choudhary, Jin dong Ding, Xiaoping Qi, Michael E. Boulton, Pei Li Yao, Jeffrey M. Peters, Goldis Malek

Research output: Contribution to journalArticlepeer-review

30 Scopus citations


Peroxisome proliferator-activated receptor-β/δ (PPARβ/δ) is a nuclear receptor that regulates differentiation, inflammation, lipid metabolism, extracellular matrix remodeling, and angiogenesis in multiple tissues. These pathways are also central to the pathogenesis of age-related macular degeneration (AMD), the leading cause of vision loss globally. With the goal of identifying signaling pathways that may be important in the development of AMD, we investigated the impact of PPARβ/δ activation on ocular tissues affected in the disease. PPARβ/δ is expressed and can be activated in AMD vulnerable cells, including retinal pigment epithelial (RPE) and choroidal endothelial cells. Further, PPARβ/δ knockdown modulates AMD-related pathways selectively. Specifically, genetic ablation of Pparβ/δ in aged mice resulted in exacerbation of several phenotypic features of early dry AMD, but attenuation of experimentally induced choroidal neovascular (CNV) lesions. Antagonizing PPARβ/δ in both in vitro angiogenesis assays and in the in vivo experimentally induced CNV model, inhibited angiogenesis and angiogenic pathways, while ligand activation of PPARβ/δ, in vitro, decreased RPE lipid accumulation, characteristic of dry AMD. This study demonstrates for the first time, selective regulation of a nuclear receptor in the eye and establishes that selective targeting of PPARβ/δ may be a suitable strategy for treatment of different clinical sub-types of AMD.

Original languageEnglish (US)
Pages (from-to)1952-1978
Number of pages27
Issue number9
StatePublished - 2016

All Science Journal Classification (ASJC) codes

  • Aging
  • Cell Biology


Dive into the research topics of 'PPARβ/δ selectively regulates phenotypic features of age-related macular degeneration'. Together they form a unique fingerprint.

Cite this