# Endothelial clock regulates retinal angiogenesis and ganglion cell function

**Authors:** Vijay K. Jidigam, Madison B. Kirby, Joshua Gallop, Brianna M. Shimandle, Dhwani Parsana, Minzhong Yu, Richard A. Lang, Sujata Rao

PMC · DOI: 10.1007/s10456-025-10018-4 · Angiogenesis · 2025-11-15

## TL;DR

This study shows that circadian clock genes Bmal1 and Per2 regulate retinal blood vessel growth and ganglion cell function.

## Contribution

The study reveals distinct roles of Bmal1 and Per2 in retinal angiogenesis and their impact on cell proliferation and retinal function.

## Key findings

- Endothelial deletion of Bmal1 and Per2 impairs retinal angiogenesis with distinct effects.
- Circadian clocks regulate VEC proliferation and influence Brn3a-positive RGC numbers.
- Disrupted circadian control leads to compromised retinal circuitry and function.

## Abstract

Angiogenesis, the formation of new blood vessels from existing ones, is essential for physiological and pathological processes such as wound healing, organ development, and tumor growth. It is a tightly regulated process influenced by both intrinsic and extrinsic factors. Emerging evidence shows a connection between biological clocks that regulate physiological rhythms and angiogenesis through the modulation of angiogenic factors like vascular growth factor (Vegfa). Thus, the clock system can directly modulate the timing and efficiency of angiogenic processes. This study aimed to investigate the role of key circadian clock genes, Bmal1 and Per2, in retinal angiogenesis. Endothelial cell-specific deletion of these genes significantly impairs vessel growth, although distinct phenotypic differences emerge between the two knockout models as angiogenesis progresses. RNA-sequencing (RNA-seq) analysis of retinal endothelial cells reveals that circadian clocks predominantly influence the expression of genes involved in cell proliferation. Notably, vascular endothelial cell (VEC) proliferation is diurnally regulated and is disrupted in Bmal1 knockout animals, leading to an increase in the number of Brn3a-positive retinal ganglion cells (RGCs). These alterations are further associated with compromised retinal circuitry and function. Thus, this study uncovers critical roles for Bmal1 and Per2 in regulating retinal angiogenesis, emphasizing the importance of circadian control of cell proliferation in vascular development and retinal function.

The online version contains supplementary material available at 10.1007/s10456-025-10018-4.

## Linked entities

- **Genes:** BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406], PER2 (period circadian regulator 2) [NCBI Gene 8864], VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422], POU4F1 (POU class 4 homeobox 1) [NCBI Gene 5457]

## Full-text entities

- **Genes:** Vegfa (vascular endothelial growth factor A) [NCBI Gene 83785] {aka VEGF-A, VEGF111, VEGF164, VPF, Vegf}, Bmal1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 29657] {aka Arntl}, Per2 (period circadian regulator 2) [NCBI Gene 63840] {aka rPER2}, Pou4f1 (POU class 4 homeobox 1) [NCBI Gene 114503] {aka Brn3a, brn-3A}
- **Diseases:** tumor (MESH:D009369)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12619741/full.md

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Source: https://tomesphere.com/paper/PMC12619741