Evidence map›Paper›PMID 36264636›Full record

ArticleJCI insight2022

Single-cell transcriptome analyses reveal microglia types associated with proliferative retinopathy.

Zhiping Liu, Huidong Shi, Jiean Xu, Qiuhua Yang, Qian Ma, Xiaoxiao Mao, Zhimin Xu, Yaqi Zhou, Qingen Da, Yongfeng Cai and 5 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
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

37 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Microglial polarization in retinal neovascularization: Friend or foe?Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Review
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  12. Sorting nexin 3 promotes ischemic retinopathy through RIP1- and RIP3-mediated myeloid cell necroptosis and mitochondrial fission.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Article
  14. Single-cell analysis identifies MKI67Journal of translational medicine · 2025
    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

15 authors at 4 institutions in 3 countries.

Zhiping LiuVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Huidong ShiGeorgia Cancer Center and.
Jiean XuVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Qiuhua YangVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Qian MaVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Xiaoxiao MaoVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Zhimin XuVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Yaqi ZhouVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Qingen DaDepartment of Cardiovascular Surgery, Peking University Shenzhen Hospital, Shenzhen, China.
Yongfeng CaiVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
David Jr FultonVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Zheng DongDepartment of Cellular Biology and Anatomy, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Akrit SodhiWilmer Eye Institute, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Ruth B CaldwellVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Yuqing HuoVascular Biology Center, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Augusta University · USJinan University · CNJohns Hopkins University · USPeking University Shenzhen Hospital · CN

Funding

Cellular Mechanisms of Retinopathy: Role of ArginaseR01EY011766 · NEI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI CALDWELL, ROBERT WILLIAM, CALDWELL, RUTH B · 1998 to 2021
$6.7M
Module 3: Gene Expression/ProteomicsP30EY031631 · NEI · AUGUSTA UNIVERSITY · PI Xingjun Fan · 2020 to 2026
$3.6M
Divergent Roles for Hypoxia-Inducible Factor-1 and -2 in Ischemic Retinal DiseaseR01EY029750 · NEI · JOHNS HOPKINS UNIVERSITY · PI SODHI, AKRIT SINGH · 2019 to 2023
$2.6M
Myeloid glycolysis in pathological ocular angiogenesisR01EY030500 · NEI · AUGUSTA UNIVERSITY · PI CALDWELL, RUTH B, HUO, YUQING · 2019 to 2023
$2.6M
Persistent STAT5 signaling in polyfunctional CD4 T cells and its application in adoptive T cell therapyR01CA264983 · NCI · AUGUSTA UNIVERSITY · PI SHI, HUIDONG, ZHOU, GANG · 2021 to 2025
$2.6M
PFKFB3 in vascular remodelingR01HL134934 · NHLBI · AUGUSTA UNIVERSITY · PI HUO, YUQING, SU, YUNCHAO · 2017 to 2020
$2.3M
Elucidation of novel anti-angiogenic therapies for the prevention and treatment of neovascular glaucomaR01EY032104 · NEI · UNIVERSITY OF MARYLAND BALTIMORE · PI MONTANER, SILVIA V, SODHI, AKRIT SINGH · 2021 to 2024
$2.3M
Adenosine receptor 2A in subretinal fibrosisR01EY033737 · NEI · BAYLOR COLLEGE OF MEDICINE · PI Ruth B Caldwell, YUQING HUO · 2022 to 2026
$2.1M
"Myeloid PFKFB3 in subretinal fibrosis"R01EY033369 · NEI · AUGUSTA UNIVERSITY · PI CALDWELL, RUTH B, HUO, YUQING · 2022 to 2025
$1.6M
BLRD VA I01 BX002035NCI NIH HHS R01 CA264983NEI NIH HHS P30 EY031631NEI NIH HHS R01 EY011766NEI NIH HHS R01 EY029750NEI NIH HHS R01 EY030500NEI NIH HHS R01 EY033369NEI NIH HHS R01 EY033737NHLBI NIH HHS R01 HL134934
6 · The paper itself

Abstract

Pathological angiogenesis is a major cause of irreversible blindness in individuals of all age groups with proliferative retinopathy (PR). Mononuclear phagocytes (MPs) within neovascular areas contribute to aberrant retinal angiogenesis. Due to their cellular heterogeneity, defining the roles of MP subsets in PR onset and progression has been challenging. Here, we aimed to investigate the heterogeneity of microglia associated with neovascularization and to characterize the transcriptional profiles and metabolic pathways of proangiogenic microglia in a mouse model of oxygen-induced PR (OIR). Using transcriptional single-cell sorting, we comprehensively mapped all microglia populations in retinas of room air (RA) and OIR mice. We have unveiled several unique types of PR-associated microglia (PRAM) and identified markers, signaling pathways, and regulons associated with these cells. Among these microglia subpopulations, we found a highly proliferative microglia subset with high self-renewal capacity and a hypermetabolic microglia subset that expresses high levels of activating microglia markers, glycolytic enzymes, and proangiogenic Igf1. IHC staining shows that these PRAM were spatially located within or around neovascular tufts. These unique types of microglia have the potential to promote retinal angiogenesis, which may have important implications for future treatment of PR and other pathological ocular angiogenesis-related diseases.

Indexed as

Single-Cell Gene Expression AnalysisAnimalsMiceProtein TransportAngiogenesisMolecular pathologyMouse modelsOphthalmologyRetinopathy

Identifiers

PMID36264636
PMCPMC9746914
OpenAlexW4306888744

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.