Evidence map›Paper›PMID 34057287›Full record

ArticleJournal of cellular and molecular medicine2021

The P300/XBP1s/Herpud1 axis promotes macrophage M2 polarization and the development of choroidal neovascularization.

Wendie Li, Ying Wang, Linling Zhu, Shu Du, Jinghai Mao, Yanyan Wang, Sangsang Wang, Qingyun Bo, Yuanyuan Tu, QuanYong Yi

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

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  20. Molecular Mechanism Underlying Role of the XBP1s in Cardiovascular Diseases.Journal of cardiovascular development and disease · 2022
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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 at 2 institutions in 1 country.

Wendie LiDepartment of Ophthalmology, Ningbo Eye Hospital, Ningbo, China.
Ying WangDepartment of Ophthalmology, Suzhou Municipal Hospital, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, China.
Linling ZhuDepartment of Ophthalmology, Lixiang Eye Hospital of Soochow University, Suzhou, China.
Shu DuDepartment of Ophthalmology, Lixiang Eye Hospital of Soochow University, Suzhou, China.
Jinghai MaoDepartment of Ophthalmology, Ningbo Eye Hospital, Ningbo, China.
Yanyan WangDepartment of Ophthalmology, Ningbo Eye Hospital, Ningbo, China.
Sangsang WangDepartment of Ophthalmology, Ningbo Eye Hospital, Ningbo, China.
Qingyun BoDepartment of Ophthalmology, Ningbo Eye Hospital, Ningbo, China.
Yuanyuan TuDepartment of Ophthalmology, Lixiang Eye Hospital of Soochow University, Suzhou, China.
QuanYong YiDepartment of Ophthalmology, Ningbo Eye Hospital, Ningbo, China.ORCID 0000-0001-6532-2519
Anyang Eye Hospital · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neovascular age-related macular degeneration (AMD), which is characterized by choroidal neovascularization (CNV), leads to vision loss. M2 macrophages produce vascular endothelial growth factor (VEGF), which aggravates CNV formation. The histone acetyltransferase p300 enhances the stability of spliced X-box binding protein 1 (XBP1s) and promotes the transcriptional activity of the XBP1s target gene homocysteine inducible endoplasmic reticulum protein with ubiquitin-like domain 1 (Herpud1). Herpud1 promotes the M2 polarization of macrophages. This study aimed to explore the roles of the p300/XBP1s/Herpud1 axis in the polarization of macrophages and the pathogenesis of CNV. Hypoxia-induced p300 interacted with XBP1s to acetylate XBP1s in RAW264.7 cells. Additionally, hypoxia-induced p300 enhanced the XBP-1s-mediated unfolded protein response (UPR), alleviated the proteasome-dependent degradation of XBP1s and enhanced the transcriptional activity of XBP1s for Herpud1. The hypoxia-induced p300/XBP1s/Herpud1 axis facilitated RAW264.7 cell M2 polarization. Knockdown of the p300/XBP1s/Herpud1 axis in RAW264.7 cells inhibited the proliferation, migration and tube formation of mouse choroidal endothelial cells (MCECs). The p300/XBP1s/Herpud1 axis increased in infiltrating M2-type macrophages in mouse laser-induced CNV lesions. Blockade of the p300/XBP1s/Herpud1 axis inhibited macrophage M2 polarization and alleviated CNV lesions. Our study demonstrated that the p300/XBP1s/Herpud1 axis in infiltrating macrophages increased the M2 polarization of macrophages and the development of CNV.

Indexed as

AnimalsChoroidChoroidal NeovascularizationDisease Models, AnimalEndothelial CellsHumansMacrophage ActivationMacrophagesMembrane ProteinsMicep300-CBP Transcription FactorsRAW 264.7 CellsSignal TransductionVascular Endothelial Growth Factor AX-Box Binding Protein 1Herpud1 protein, mouseMembrane Proteinsp300-CBP Transcription FactorsVascular Endothelial Growth Factor AX-Box Binding Protein 1Xbp1 protein, mousechoroidal neovascularizationHerpud1macrophage polarizationp300XBP1s

Identifiers

PMID34057287
PMCPMC8278076
OpenAlexW3165597912

What OpenQuestion holds

Textmetadata
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.