# Local Insulin for Local Needs? Insights into Retinal Insulin Signaling and RPE Metabolism

**Authors:** Matilde Balbi, Alessandra Puddu, Andrea Amaroli, Davide Maggi, Isabella Panfoli, Silvia Ravera

PMC · DOI: 10.3390/biom15111570 · 2025-11-08

## TL;DR

This review explores how the retina's own insulin production may support eye health and prevent degeneration, even when the body's insulin is low.

## Contribution

The paper highlights new evidence that the retinal pigment epithelium produces insulin locally, potentially sustaining retinal function independently of systemic insulin.

## Key findings

- The retinal pigment epithelium (RPE) synthesizes and secretes insulin, possibly in response to photoreceptor outer segment phagocytosis.
- Local insulin signaling in the retina may maintain glucose uptake, lipid metabolism, and neurovascular integrity even under systemic insulin deficiency.
- Impaired retinal insulin signaling is linked to diabetic retinopathy and other degenerative retinal diseases.

## Abstract

Insulin is a key anabolic hormone traditionally considered to be exclusively produced by pancreatic β-cells. Insulin exerts several systemic effects involved in glucose uptake and metabolism. In the retina, insulin signaling acts as a regulator of photoreceptor- retinal pigment epithelium (RPE) metabolic coupling as well as of neuronal survival via the PI3K/Akt and MAPK/ERK pathways. Impaired insulin signaling contributes to diabetic retinopathy, retinitis pigmentosa, and age-related degeneration by disrupting energy homeostasis and trophic support. However, growing evidence suggests that the retina, particularly RPE, locally synthesizes and secretes insulin. Although the role of local insulin production in the retina remains to be clarified, this discovery introduces a paradigm shift in retinal physiology, suggesting a self-sustaining insulin signaling system that supports glucose uptake, lipid metabolism, and neurovascular integrity. Emerging data indicate that RPE-derived insulin is stimulated by photoreceptor outer segment (POS) phagocytosis and may act through autocrine and paracrine mechanisms to maintain retinal function, even under conditions of systemic insulin deficiency. Understanding this extra-pancreatic insulin source opens new therapeutic perspectives aimed at enhancing local insulin signaling to preserve vision and prevent retinal degeneration. Thus, the objective of this review is to summarize current evidence on RPE-derived insulin and to discuss its potential implications for retinal homeostasis and disease.

## Linked entities

- **Proteins:** PIN (insulin precursor), PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), AKT1 (AKT serine/threonine kinase 1), MAPK (mitogen activated kinase-like protein), EPHB2 (EPH receptor B2)
- **Diseases:** diabetic retinopathy (MONDO:0005266), retinitis pigmentosa (MONDO:0008377)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}
- **Diseases:** retinitis pigmentosa (MESH:D012174), diabetic retinopathy (MESH:D003930), insulin deficiency (MESH:D007333), retinal degeneration (MESH:D012162), age-related degeneration (MESH:D008268)
- **Chemicals:** lipid (MESH:D008055), glucose (MESH:D005947)
- **Cell lines:** RPE — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_IQ82)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12650497/full.md

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Source: https://tomesphere.com/paper/PMC12650497