Evidence map›Paper›PMID 32213707›Full record

ArticleJCI insight2020

iPSC-derived endothelial cell response to hypoxia via SDF1a/CXCR4 axis facilitates incorporation to revascularize ischemic retina.

Hongkwan Cho, Bria L Macklin, Ying-Yu Lin, Lingli Zhou, Michael J Lai, Grace Lee, Sharon Gerecht, Elia J Duh

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 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

8 authors at 2 institutions in 1 country.

Hongkwan ChoDepartment of Ophthalmology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Bria L MacklinDepartment of Chemical and Biomolecular Engineering, Institute for NanoBioTechnology, Johns Hopkins University Baltimore, Maryland, USA.
Ying-Yu LinDepartment of Chemical and Biomolecular Engineering, Institute for NanoBioTechnology, Johns Hopkins University Baltimore, Maryland, USA.
Lingli ZhouDepartment of Ophthalmology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Michael J LaiDepartment of Ophthalmology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Grace LeeDepartment of Ophthalmology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Sharon GerechtDepartment of Chemical and Biomolecular Engineering, Institute for NanoBioTechnology, Johns Hopkins University Baltimore, Maryland, USA.
Elia J DuhDepartment of Ophthalmology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI Jiang Qian · 1985 to 2026
$22.1M
Regulation of diabetic retinopathy by Nrf2R01EY022383 · NEI · JOHNS HOPKINS UNIVERSITY · PI DUH, ELIA J · 2012 to 2020
$3.8M
Role of Nrf2 in retinal vascularization and ROPR01EY022683 · NEI · JOHNS HOPKINS UNIVERSITY · PI DUH, ELIA J · 2012 to 2021
$3.6M
Exploring the role of hypoxia in human pluripotent stem cell derived endothelial cell vascular network formation and pericyteF31HL143972 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI MACKLIN, BRIA · 2018 to 2020
$133k
NEI NIH HHS P30 EY001765NEI NIH HHS R01 EY022383NEI NIH HHS R01 EY022683NHLBI NIH HHS F31 HL143972
6 · The paper itself

Abstract

Ischemic retinopathies are major causes of blindness worldwide. Local hypoxia created by loss of vascular supply leads to tissue injury and aberrant neovascularization in the retina. There is a great need for therapies that enhance revascularization of hypoxic neuroretinal tissue. To test the therapeutic feasibility of human-induced pluripotent stem cell-derived endothelial cells (hiPSC-ECs) for the treatment of ischemic retinopathies, we compared the angiogenic potential of hiPSC-ECs with mature human retinal endothelial cells (HRECs) in response to hypoxia. hiPSC-ECs formed more robust and complex vascular networks in collagen gels, whereas HRECs displayed minimal sprouting. The cells were further tested in the mouse oxygen-induced retinopathy (OIR) model. Retinas with hiPSC-EC injection showed colocalization with host vessels, whereas HRECs lacked such responses. hiPSC-ECs markedly reduced vaso-obliteration and pathological neovascularization. This beneficial effect of hiPSC-ECs was explained by the stromal cell-derived factor-1a (SDF1a)/CXCR4 axis; hiPSC-ECs exhibited much higher cell-surface expression of CXCR4 than HRECs and greater chemotaxis toward SDF1a-embedded 3D collagen hydrogel. Furthermore, treatment with neutralizing antibody to CXCR4 abolished recruitment of hiPSCs in the OIR model. These findings suggest superior angiogenic potential of hiPSC-ECs under hypoxia and underscore the importance of SDF1a/CXCR4 in the reparative function of hiPSC-ECs in ischemic diseases.

Indexed as

AnimalsCell HypoxiaChemokine CXCL12Endothelial CellsHumansInduced Pluripotent Stem CellsIschemiaMiceNeovascularization, PhysiologicReceptors, CXCR4Retinal DiseasesChemokine CXCL12Receptors, CXCR4endothelial cellsHuman stem cellshypoxiaStem cellsVascular Biology

Identifiers

PMID32213707
PMCPMC7213794
OpenAlexW3013074195

What OpenQuestion holds

Textmetadata
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.