Evidence map›Paper›PMID 37803306›Full record

ArticleBMC ophthalmology2023

Dynamic changes in macrophage morphology during the progression of choroidal neovascularization in a laser-induced choroidal neovascularization mouse model.

Nana Xu, Tao Sun, Yulan Wang, Xiaowei Tong, Shiheng Lu, Fan Yang, Jing Wang, Qiyu Bo, Junran Sun, Xiaodong Sun

Abstract read
In one paragraph

Article in BMC ophthalmology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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.

Nana XuShanghai Eye Diseases Prevention & Treatment Center/ Shanghai Eye Hospital, Shanghai, China.
Tao SunShanghai Eye Diseases Prevention & Treatment Center/ Shanghai Eye Hospital, Shanghai, China.
Yulan WangShanghai Eye Diseases Prevention & Treatment Center/ Shanghai Eye Hospital, Shanghai, China.
Xiaowei TongShanghai Eye Diseases Prevention & Treatment Center/ Shanghai Eye Hospital, Shanghai, China.
Shiheng LuShanghai Eye Diseases Prevention & Treatment Center/ Shanghai Eye Hospital, Shanghai, China.
Fan YangShanghai Eye Diseases Prevention & Treatment Center/ Shanghai Eye Hospital, Shanghai, China.
Jing WangShanghai Eye Diseases Prevention & Treatment Center/ Shanghai Eye Hospital, Shanghai, China.
Qiyu BoDepartment of Ophthalmology, Shanghai General Hospital (Shanghai First People's Hospital), Shanghai Jiao Tong University School of Medicine, 100 Haining Road, Shanghai, 200080, China.
Junran SunDepartment of Ophthalmology, Shanghai General Hospital (Shanghai First People's Hospital), Shanghai Jiao Tong University School of Medicine, 100 Haining Road, Shanghai, 200080, China. emiliesun@sina.com.
Xiaodong SunDepartment of Ophthalmology, Shanghai General Hospital (Shanghai First People's Hospital), Shanghai Jiao Tong University School of Medicine, 100 Haining Road, Shanghai, 200080, China.

Funding

A three-year action plan for TCM inheritance, innovation and development ZY(2021-2023)-0207-01National Natural Science Foundation of China 82171076Shanghai Collaborative Innovation Center for Translational Medicine TM202115PTShanghai eye hospital in-hospital foundation 2021JC003Shanghai Hospital Development Center SHDC2020CR2040B, SHDC2020CR5014, SHDC12020111
6 · The paper itself

Abstract

backgroundNeovascular age-related macular degeneration (AMD) is responsible for the majority of severe vision loss cases and is mainly caused by choroidal neovascularization (CNV). This condition persists or recurs in a subset of patients and regresses after 5 or more years of anti-vascular endothelial growth factor (VEGF) treatment. The precise mechanisms of CNV continue to be elucidated. According to our previous studies, macrophages play a critical role in CNV. Herein, we aimed to determine the morphological changes in macrophages in CNV to help us understand the dynamic changes.

methodsMice were subjected to laser injury to induce CNV, and lesion expansion and macrophage transformation were examined by immunofluorescence and confocal analysis. Several strategies were used to verify the dynamic changes in macrophages. Immunofluorescence and confocal assays were performed on choroidal flat mounts to evaluate the morphology and phenotype of macrophages in different CNV phases, and the results were further verified by western blotting and RT-PCR.

resultsThe location of infiltrated macrophages changed after laser injury in the CNV mouse model, and macrophage morphology also dynamically changed. Branching macrophages gradually shifted to become round with the progression of CNV, which was certified to be an M2 phenotypic shift.

conclusionsDynamic changes in macrophage morphology were observed during CNV formation, and the round-shaped M2 phenotype could promote neovascularization. In general, the changes in morphology we observed in this study can help us to understand the critical role of macrophages in CNV progression and exploit a potential treatment option for CNV indicated by a shift in macrophage polarity.

Indexed as

Choroidal NeovascularizationAnimalsChoroidDisease Models, AnimalHumansLasersMacrophagesMiceMice, Inbred C57BLChoroidal neovascularizationMacrophageMorphology

Identifiers

PMID37803306
PMCPMC10559478

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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.