Evidence map›Paper›PMID 36813133›Full record

ArticleThe ocular surface2023

Novel characterization of CXCR4 expressing cells in uninfected and herpes simplex virus-1 infected corneas.

Pratima Krishna Suvas, Mizumi Setia, Mashidur Rana, Anish Chakraborty, Susmit Suvas

Open access · greenAbstract read
In one paragraph

Article in The ocular surface, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Pratima Krishna SuvasDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA.
Mizumi SetiaDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA.
Mashidur RanaDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA.
Anish ChakrabortyDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA.
Susmit SuvasDepartment of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, USA. Electronic address: ssuvas@med.wayne.edu.
Wayne State University · US

Funding

VISION RESEARCH--COREP30EY004068 · NEI · WAYNE STATE UNIVERSITY · PI LINDA D HAZLETT · 1985 to 2026
$13.2M
Interplay between hypoxia and oxidative phosphorylation in herpes stromal keratitisR01EY029690 · NEI · WAYNE STATE UNIVERSITY · PI SUVAS, SUSMIT · 2019 to 2023
$2.1M
Role of insulin-like growth factor binding proteins in the pathogenesis of herpes stromal keratitis.R01EY030129 · NEI · WAYNE STATE UNIVERSITY · PI SUVAS, SUSMIT · 2020 to 2024
$1.9M
CXCR4: A potential therapeutic target in HSKR01EY035540 · NEI · WAYNE STATE UNIVERSITY · PI Susmit Suvas · 2023 to 2026
$1.5M
NEI NIH HHS P30 EY004068NEI NIH HHS R01 EY029690NEI NIH HHS R01 EY030129NEI NIH HHS R01 EY035540
6 · The paper itself

Abstract

purposeTo characterize CXCR4-expressing cells in uninfected and herpes simplex virus-1 (HSV-1) infected corneas.

methodsThe corneas of C57BL/6J mice were infected with HSV-1 McKrae. The RT-qPCR assay detected CXCR4 and CXCL12 transcripts in uninfected and HSV-1-infected corneas. Immunofluorescence staining for CXCR4 and CXCL12 protein was performed in the frozen sections of herpes stromal keratitis (HSK) corneas. Flow cytometry assay characterized the CXCR4-expressing cells in uninfected and HSV-1-infected corneas.

resultsFlow cytometry data showed CXCR4 expressing cells in the separated epithelium and stroma of uninfected corneas. In the uninfected stroma, CD11b + F4/80+ macrophages are the predominant CXCR4-expressing cells. In contrast, most CXCR4 expressing cells in the uninfected epithelium were CD207 (langerin)+, CD11c+, and expressed MHC class II molecule, documenting the Langerhans cells (LCs) phenotype. After corneal HSV-1 infection, CXCR4 and CXCL12 mRNA levels increased significantly in HSK corneas than in uninfected corneas. Immunofluorescence staining showed CXCR4 and CXCL12 protein localization in the newly formed blood vessels in the HSK cornea. Furthermore, the infection resulted in LCs proliferation, causing an increase in their numbers in the epithelium at 4 days post-infection (p.i.). However, by 9-day p.i., the LCs numbers declined to the counts observed in naïve corneal epithelium. Our results also showed neutrophils and vascular endothelial cells as the prominent CXCR4-expressing cell types in the stroma of HSK corneas.

conclusionsTogether, our data demonstrate the expression of CXCR4 on resident antigen presenting cells in the uninfected cornea and on infiltrating neutrophils and newly formed blood vessels in the HSK cornea.

Indexed as

Herpesvirus 1, HumanKeratitis, HerpeticAnimalsCorneaEndothelial CellsMiceMice, Inbred C57BLReceptors, CXCR4CXCR4 protein, mouseReceptors, CXCR4Chemokine receptorCorneaHerpes simplex virusLangerhans cell

Identifiers

PMID36813133
PMCPMC10439974
OpenAlexW4321368399

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Registered trials

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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.