# Activated Protein C and the Retina: From Physiology to Therapeutic Potential

**Authors:** Alon Zahavi, Sarina Levy-Mendelovich, John H. Griffin, Tami Livnat

PMC · DOI: 10.3390/ijms27052282 · International Journal of Molecular Sciences · 2026-02-28

## TL;DR

This paper reviews the role of activated protein C in retinal health and its potential as a treatment for retinal diseases.

## Contribution

The paper highlights the therapeutic potential of 3K3A-APC for retinal pathologies based on preclinical findings.

## Key findings

- APC contributes to retinal integrity and vascular homeostasis under normal conditions.
- 3K3A-APC can cross the blood–retina barrier and induce cytoprotective effects in the retina.
- Congenital PC deficiency is linked to severe ocular complications, emphasizing APC's importance.

## Abstract

Protein C (PC) and its activated form, activated protein C (APC), are well-established regulators of coagulation and cytoprotection. While their systemic functions are extensively characterized, their physiological roles in the retina have only recently begun to be explored. This gap persists despite the observation that congenital PC deficiency is consistently associated with severe ocular complications. Emerging evidence, including the development of a murine model of severe protein C deficiency (SPCD), indicates that APC contributes to retinal integrity and vascular homeostasis under physiological conditions. Beyond its physiological function, APC has shown therapeutic activity in several models of retinal disease. Recent findings from our group further demonstrated that intravenously administered APC and its cytoprotective analog, 3K3A-APC, can cross the blood–retina barrier via the endothelial protein C receptor (EPCR), despite their relatively large molecular weight (~62 kDa), and induce cytoprotective activities in the retina. These findings highlight the translational potential of 3K3A-APC and support its further development as a systemically delivered therapeutic approach for retinal pathologies. This review integrates current knowledge of the molecular biology of the PC/APC pathways with its emerging physiological functions in the retina, and the accumulating preclinical and early clinical evidence that supports its therapeutic relevance.

## Linked entities

- **Proteins:** APC (APC regulator of Wnt signaling pathway), PROCR (protein C receptor)

## Full-text entities

- **Genes:** Proc (protein C) [NCBI Gene 19123] {aka PC}, Pcx (pyruvate carboxylase) [NCBI Gene 18563] {aka Pc, Pcb}, Procr (protein C receptor, endothelial) [NCBI Gene 19124] {aka Ccca, Ccd41, Epcr}, Apc (APC, WNT signaling pathway regulator) [NCBI Gene 11789] {aka CC1, Min, mAPC}
- **Diseases:** SPCD (MESH:D045169), congenital PC deficiency (MESH:D020151), retinal disease (MESH:D012164)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12984644/full.md

## References

90 references — full list in the complete paper: https://tomesphere.com/paper/PMC12984644/full.md

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Source: https://tomesphere.com/paper/PMC12984644