
CLC number:
On-line Access: 2025-10-21
Received: 2025-03-27
Revision Accepted: 2025-05-15
Crosschecked: 2025-10-21
Cited: 0
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Citations: Bibtex RefMan EndNote GB/T7714
Kun ZHAO, Yaping JIANG, Wen HUANG, Yukang MAO, Yihui CHEN, Peng LI, Chuanxi YANG. Alamandine inhibits pathological retinal neovascularization by targeting the MrgD-mediated HIF-1α/VEGF pathway[J]. Journal of Zhejiang University Science B, 2025, 26(10): 1015-1036.
@article{title="Alamandine inhibits pathological retinal neovascularization by targeting the MrgD-mediated HIF-1α/VEGF pathway",
author="Kun ZHAO, Yaping JIANG, Wen HUANG, Yukang MAO, Yihui CHEN, Peng LI, Chuanxi YANG",
journal="Journal of Zhejiang University Science B",
volume="26",
number="10",
pages="1015-1036",
year="2025",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B2500154"
}
%0 Journal Article
%T Alamandine inhibits pathological retinal neovascularization by targeting the MrgD-mediated HIF-1α/VEGF pathway
%A Kun ZHAO
%A Yaping JIANG
%A Wen HUANG
%A Yukang MAO
%A Yihui CHEN
%A Peng LI
%A Chuanxi YANG
%J Journal of Zhejiang University SCIENCE B
%V 26
%N 10
%P 1015-1036
%@ 1673-1581
%D 2025
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B2500154
TY - JOUR
T1 - Alamandine inhibits pathological retinal neovascularization by targeting the MrgD-mediated HIF-1α/VEGF pathway
A1 - Kun ZHAO
A1 - Yaping JIANG
A1 - Wen HUANG
A1 - Yukang MAO
A1 - Yihui CHEN
A1 - Peng LI
A1 - Chuanxi YANG
J0 - Journal of Zhejiang University Science B
VL - 26
IS - 10
SP - 1015
EP - 1036
%@ 1673-1581
Y1 - 2025
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B2500154
Abstract: retinopathy of prematurity (ROP) is a vision-threatening disorder that leads to pathological growth of the retinal vasculature due to hypoxia. Here, we investigated the potential effects of alamandine, a novel heptapeptide in the renin-angiotensin system (RAS), on hypoxia-induced retinal neovascularization and its underlying mechanisms. In vivo, the C57BL/6J mice with oxygen-induced retinopathy (OIR) were injected intravitreally with alamandine (1.0 μmol/kg per eye). In vitro, human retinal microvascular endothelial cells (HRMECs) were utilized to investigate the effects of alamandine (10 μg/mL) on proliferation, apoptosis, migration, and tubular formation under vascular endothelial growth factor (VEGF) stimulation. Single-cell RNA sequencing (scRNA-seq) matrix data from the Gene Expression Omnibus (GEO) database and RAS-related genes from the Molecular Signatures Database (MSigDB) were sourced for subsequent analyses. By integrating scRNA-seq data across multiple species, we identified that RAS-associated endothelial cell populations were highly related to retinal neovascularization. The liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis revealed a significant decrease in alamandine levels in both the serum and retina of OIR mice compared to those in the control group. Next, alamandine ameliorated hypoxia-induced retinal pathological neovascularization and physiologic revascularization in OIR mice. In vitro, alamandine effectively mitigated VEGF-induced proliferation, scratch wound healing, and tube formation of HRMECs primarily by inhibiting the hypoxia-inducible factor-1α (HIF-1α)/VEGF pathway. Further, coincubation with D-Pro7 (mas-related G protein-coupled receptor D (MrgD) antagonist) hindered the beneficial impacts of alamandine on hypoxia-induced pathological angiogenesis both in vivo and in vitro. Our findings suggested that alamandine could mitigate retinal neovascularization by targeting the MrgD-mediated HIF-1α/VEGF pathway, providing a potential therapeutic agent for OIR prevention and treatment.
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