Regulators of retinal metabolism in healthy and degenerating retinas

NIH RePORTER · NIH · R01 · $440,322 · view on reporter.nih.gov ↗

Abstract

Abstract: The retina has high metabolic activity, and retinal degenerations have been associated with mitochondrial dysfunction, dysregulation of metabolism, and toxic oxidative damage. However, little is known about how metabolism is maintained under normal conditions or is dysregulated in degenerating retinas. AMPK (AMP- activated protein kinase) is a key regulator of metabolism in highly metabolic tissues and is a candidate to regulate metabolism in photoreceptors, and its role in retinal metabolism will be rigorously studied in this proposed project using both gain-of-function and loss-of-function approaches. Peroxisome proliferator-activated receptor gamma coactivator-alpha (PGC-1α) and beta (PGC-1β) are key regulators of mitochondrial biogenesis. Adenosine monophosphate dependent kinase (AMPK) is an important regulator of PGC-1 activity. Our goal in this study is to determine the roles of AMPK and PGC-1 activity in retinal photoreceptors.

Key facts

NIH application ID
10247603
Project number
5R01EY031720-02
Recipient
UNIVERSITY OF FLORIDA
Principal Investigator
John D Ash
Activity code
R01
Funding institute
NIH
Fiscal year
2021
Award amount
$440,322
Award type
5
Project period
2020-09-01 → 2025-06-30