RPE cell signaling linked to choroid damage in macular degeneration

Aberrant RPE mTORC1 signaling in dysregulation of choroid homeostasis

NIH-funded research University of Texas Hlth Sci Ctr Houston · NIH-11479819

This work looks at whether overactive signaling in retinal pigment cells causes loss of the blood-vessel layer under the retina in people with age-related macular degeneration.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Texas Hlth Sci Ctr Houston NIH-funded
Lab location1 site (Houston, United States)
Project IDNIH-11479819 on NIH RePORTER

What this research studies

Researchers are studying how overactive mTORC1 signaling in the retinal pigment epithelium (RPE) may cause the choriocapillaris (the blood-vessel layer under the retina) to shrink. They use mouse models with RPE-specific mTORC1 activation, measure ANGPT2 levels released by RPE, and test whether the phosphoprotein DARPP-32 controls that secretion. The team combines molecular lab experiments, cell studies, and choroidal imaging to trace how RPE dysfunction leads to vessel loss beneath the retina. Results could identify targets to prevent or slow choroidal atrophy in AMD.

Who could benefit from this research

Good fit: People with age-related macular degeneration, especially those with early choroidal thinning or signs of RPE dysfunction, would be most relevant for follow-up studies or future trials based on this work.

Not a fit: Patients whose vision loss is due to other retinal diseases (such as diabetic retinopathy or glaucoma) or those with very advanced, irreversible retinal damage may not benefit from findings focused on choroidal protection.

Why it matters

Potential benefit: If successful, this work could point to new treatments that protect the choroid and slow vision loss in age-related macular degeneration.

How similar studies have performed: Previous studies targeting ANGPT2/Tie2 signaling in eye disease have shown promise in animal models, but the proposed link from RPE mTORC1 through DARPP-32 to ANGPT2 secretion is a novel mechanism.

Where this research is happening

Houston, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.