Evidence map›Paper›PMID 37917183›Full record

ArticleJCI insight2023

Single-cell transcriptomics analysis of proliferative diabetic retinopathy fibrovascular membranes reveals AEBP1 as fibrogenesis modulator.

Katia Corano Scheri, Jeremy A Lavine, Thomas Tedeschi, Benjamin R Thomson, Amani A Fawzi

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
11.4field-weighted citation impact, top 1% 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

40 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article
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.

Katia Corano ScheriDepartment of Ophthalmology and.
Jeremy A LavineDepartment of Ophthalmology and.
Thomas TedeschiDepartment of Ophthalmology and.
Benjamin R ThomsonDepartment of Ophthalmology and.
Amani A FawziDepartment of Ophthalmology and.
Northwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Devalingam Mahalingam · 1993 to 2026
$153.9M
Exploring the angiogenesis-to-fibrosis transition in ischemic retinopathies RenewalR01EY030121 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Amani A Fawzi · 2020 to 2026
$2.9M
The role of Angiopoietin-TEK signaling in polypoidal choroidal vasculopathyR01EY032609 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI THOMSON, BENJAMIN R. · 2021 to 2025
$2.0M
Investigating the function and mechanism of interleukin 7 receptor-expressing pro-angiogenic macrophages during experimental choroidal neovascularizationR01EY034486 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Jeremy A Lavine · 2023 to 2026
$1.6M
The role of beta2-adrenergic receptor and interleukin-6 signaling in macrophage-driven choroidal neovascularizationK08EY030923 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LAVINE, JEREMY A · 2020 to 2024
$972k
NCI NIH HHS P30 CA060553NEI NIH HHS K08 EY030923NEI NIH HHS R01 EY030121NEI NIH HHS R01 EY032609NEI NIH HHS R01 EY034486
6 · The paper itself

Abstract

The management of preretinal fibrovascular membranes, a devastating complication of advanced diabetic retinopathy (DR), remains challenging. We characterized the molecular profile of cell populations in these fibrovascular membranes to identify potentially new therapeutic targets. Preretinal fibrovascular membranes were surgically removed from patients and submitted for single-cell RNA-Seq (scRNA-Seq). Differential gene expression was implemented to define the transcriptomics profile of these cells and revealed the presence of endothelial, inflammatory, and stromal cells. Endothelial cell reclustering identified subclusters characterized by noncanonical transcriptomics profile and active angiogenesis. Deeper investigation of the inflammatory cells showed a subcluster of macrophages expressing proangiogenic cytokines, presumably contributing to angiogenesis. The stromal cell cluster included a pericyte-myofibroblast transdifferentiating subcluster, indicating the involvement of pericytes in fibrogenesis. Differentially expressed gene analysis showed that Adipocyte Enhancer-binding Protein 1, AEBP1, was significantly upregulated in myofibroblast clusters, suggesting that this molecule may have a role in transformation. Cell culture experiments with human retinal pericytes (HRP) in high-glucose condition confirmed the molecular transformation of pericytes toward myofibroblastic lineage. AEBP1 siRNA transfection in HRP reduced the expression of profibrotic markers in high glucose. In conclusion, AEBP1 signaling modulates pericyte-myofibroblast transformation, suggesting that targeting AEBP1 could prevent scar tissue formation in advanced DR.

Indexed as

Diabetes MellitusDiabetic RetinopathyCarboxypeptidasesGene Expression ProfilingGlucoseHumansPericytesRepressor ProteinsRetinaAEBP1 protein, humanCarboxypeptidasesGlucoseRepressor ProteinsAngiogenesisDiabetesFibrosisOphthalmologyPericytes

Identifiers

PMID37917183
PMCPMC10896003
OpenAlexW4388219780

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.