# The role of beta2-adrenergic receptor and interleukin-6 signaling in macrophage-driven choroidal neovascularization

> **NIH NIH K08** · NORTHWESTERN UNIVERSITY · 2021 · $220,045

## Abstract

PROJECT SUMMARY:
Candidate and Career Development Plan: Dr. Lavine is a vitreoretinal surgeon, physician-scientist, and
Assistant Professor of Ophthalmology at Northwestern University. Dr. Lavine had a successful PhD, laying his
strong scientific foundation, and has successfully balanced clinical duties with productive, basic science research
in ophthalmology for the past 8 years of clinical training. His long-term career goal is to identify novel cellular and
molecular targets of the innate immune system for anti-angiogenic therapy in order to move vitreoretinal
specialists past the anti-vascular endothelial growth factor (VEGF) era and into individualized medicine. To
accomplish this, his immediate goal is to develop his career as a funded, independent physician-scientist with
expertise in the intersection of inflammation and angiogenesis. This K08 award will help achieve these goals by
developing Dr. Lavine’s scientific and professional skills in advanced immunology and bio-informatics. Dr. Lavine
and his co-mentors, Dr. Perlman and Dr. Quaggin, have developed a detailed strategy to achieve these
objectives through carefully planned course work, didactics, laboratory techniques, and collaborations at
Northwestern University. The current proposal will lay the foundation for future R01-level proposals on the
intersection between innate immunity and angiogenesis in choroidal neovascularization (CNV).
Research Plan: Neovascular age-related macular degeneration (nAMD) is the leading cause of blindness in the
developed world, and is treated solely by inhibiting VEGF. Although highly effective, 15% of patients still lose
vision despite maximal anti-VEGF therapy. Evidence suggests a role for pro-angiogenic macrophages in nAMD
pathogenesis, but currently there are no therapies to specifically target these cells. Interleukin-6 (IL-6), a pro-
inflammatory cytokine known to be produced by macrophages, correlates with nAMD activity and is necessary
for laser-induced CNV, a mouse model of nAMD. Our preliminary data demonstrate that beta2-adrenergic
receptor (AR) inhibition decreases laser-induced CNV area by reducing IL-6 levels in macrophages. Our central
hypothesis is that beta2-AR signaling influences macrophage differentiation, promotes a pro-angiogenic
macrophage phenotype, increases IL-6 levels, and activates angiogenesis by activating the IL-6 receptor directly
on endothelial cells to increase CNV area. To test this hypothesis, we formulated the following specific aims:
1) Determine the retinal/choroidal cell type(s) that express interleukin-6 in response to beta2-AR antagonism
2) Identify the cell type that produces IL-6 and the cell type that responds to IL-6 to increase laser-induced CNV.
3) Delineate how beta2-AR and IL-6 deficiency regulate the transcriptional profile of macrophages during CNV.
Completion of these aims will determine the cell types that respond to beta2-AR antagonism, produce IL-6, and
respond to IL-6 to increase CNV area. These...

## Key facts

- **NIH application ID:** 10085645
- **Project number:** 5K08EY030923-02
- **Recipient organization:** NORTHWESTERN UNIVERSITY
- **Principal Investigator:** Jeremy A Lavine
- **Activity code:** K08 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $220,045
- **Award type:** 5
- **Project period:** 2020-02-01 → 2025-01-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10085645

## Citation

> US National Institutes of Health, RePORTER application 10085645, The role of beta2-adrenergic receptor and interleukin-6 signaling in macrophage-driven choroidal neovascularization (5K08EY030923-02). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/10085645. Licensed CC0.

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