Evidence map›Paper›PMID 40164822›Full record

ArticleCommunications biology2025

OPN3-mediated positive regulation of angiogenesis in HUVECs through VEGFR2 interaction.

Huanhuan Luo, Wei Zhang, Wen Zeng, Yu Wang, Jianglong Feng, Yinghua Lan, Xian Dong, Ting Liu, Yan Sun, Hongguang Lu

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Huanhuan Luo *School of Public Health, Guizhou Medical University, Guiyang, Guizhou, China.
Wei Zhang *Department of Dermatology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Wen Zeng *Department of Dermatology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Yu Wang *Department of Dermatology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Jianglong FengDepartment of Dermatology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Yinghua LanDepartment of Dermatology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Xian DongDepartment of Dermatology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Ting LiuDepartment of Dermatology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Yan SunDepartment of Dermatology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Hongguang LuSchool of Public Health, Guizhou Medical University, Guiyang, Guizhou, China. luhongguang@gmc.edu.cn.ORCID http://orcid.org/0000-0002-5002-4276

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82173397National Natural Science Foundation of China (National Science Foundation of China) 82260615National Natural Science Foundation of China (National Science Foundation of China) 82360458National Natural Science Foundation of China (National Science Foundation of China) 82404116
6 · The paper itself

Abstract

Many rhodopsin-like G-protein-coupled receptors (Rh-GPCRs) are known to either promote or inhibit angiogenesis. Among these, Opsin 4 and Opsin 5 are specifically involved in vascular development within the eye. Opsin 3 (OPN3), another member of Rh-GPCRs, performs a variety of light-dependent and light-independent functions in extraocular tissue. However, its role in endothelial cells and angiogenesis remains unclear. Here, we found that OPN3 knockdown or knockout in zebrafish impairs embryonic angiogenesis and vascular development. Similarly, silencing OPN3 in human umbilical vein endothelial cells (HUVECs) inhibits cellular proliferation, migration, sprouting, and tube formation, while OPN3 overexpression promotes these cellular processes. Moreover, OPN3 regulates angiogenesis in HUVECs through the VEGFR2-AKT pathway, with OPN3 and VEGFR2 co-localizing at the plasma membrane and forming a physical complex. These findings provide new insights into the non-light-dependent functions of OPN3 in angiogenesis, expanding our understanding of its physiological roles and offering potential therapeutic strategies for angiogenesis-related diseases.

Indexed as

Human Umbilical Vein Endothelial CellsNeovascularization, PhysiologicRod OpsinsVascular Endothelial Growth Factor Receptor-2Zebrafish ProteinsAngiogenesisAnimalsCell MovementCell ProliferationHumansSignal TransductionZebrafishKDR protein, humanRod OpsinsVascular Endothelial Growth Factor Receptor-2Zebrafish Proteins

Identifiers

PMID40164822
PMCPMC11958745

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.