Evidence map›Paper›PMID 38023728›Full record

ArticleBioengineering & translational medicine2023

Modeling diabetic endothelial dysfunction with patient-specific induced pluripotent stem cells.

Rayyan Gorashi, Nancy Rivera-Bolanos, Caitlyn Dang, Cedric Chai, Beatrix Kovacs, Sara Alharbi, Syeda Subia Ahmed, Yogesh Goyal, Guillermo Ameer, Bin Jiang

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-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

11 citing papers in PubMed, 16 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

10 authors at 1 institution in 1 country.

Rayyan GorashiDepartment of Biomedical Engineering Northwestern University Evanston and Chicago Illinois USA.
Nancy Rivera-BolanosDepartment of Biomedical Engineering Northwestern University Evanston and Chicago Illinois USA.
Caitlyn DangDepartment of Surgery Feinberg School of Medicine, Northwestern University Chicago Illinois USA.
Cedric ChaiDepartment of Cell and Developmental Biology Northwestern University Feinberg School of Medicine Chicago Illinois USA.
Beatrix KovacsDepartment of Surgery Feinberg School of Medicine, Northwestern University Chicago Illinois USA.
Sara AlharbiDepartment of Surgery Feinberg School of Medicine, Northwestern University Chicago Illinois USA.
Syeda Subia AhmedDepartment of Cell and Developmental Biology Northwestern University Feinberg School of Medicine Chicago Illinois USA.
Yogesh GoyalDepartment of Cell and Developmental Biology Northwestern University Feinberg School of Medicine Chicago Illinois USA.
Guillermo AmeerDepartment of Biomedical Engineering Northwestern University Evanston and Chicago Illinois USA.
Bin JiangDepartment of Biomedical Engineering Northwestern University Evanston and Chicago Illinois USA.ORCID https://orcid.org/0000-0003-2390-4312
Northwestern University · US

Funding

Preclinical Investigation of a Bioengineered Vascular GraftR01EB017129 · NIBIB · NORTHWESTERN UNIVERSITY · PI AMEER, GUILLERMO ANTONIO, KIBBE, MELINA RAE · 2013 to 2016
$1.8M
NIBIB NIH HHS R01 EB017129
6 · The paper itself

Abstract

Diabetes is a known risk factor for various cardiovascular complications, mediated by endothelial dysfunction. Despite the high prevalence of this metabolic disorder, there is a lack of in vitro models that recapitulate the complexity of genetic and environmental factors associated with diabetic endothelial dysfunction. Here, we utilized human induced pluripotent stem cell (iPSC)-derived endothelial cells (ECs) to develop in vitro models of diabetic endothelial dysfunction. We found that the diabetic phenotype was recapitulated in diabetic patient-derived iPSC-ECs, even in the absence of a diabetogenic environment. Subsequent exposure to culture conditions that mimic the diabetic clinical chemistry induced a diabetic phenotype in healthy iPSC-ECs but did not affect the already dysfunctional diabetic iPSC-ECs. RNA-seq analysis revealed extensive transcriptome-wide differences between cells derived from healthy individuals and diabetic patients. The in vitro disease models were used as a screening platform which identified angiotensin receptor blockers (ARBs) that improved endothelial function in vitro for each patient. In summary, we present in vitro models of diabetic endothelial dysfunction using iPSC technology, taking into account the complexity of genetic and environmental factors in the metabolic disorder. Our study provides novel insights into the pathophysiology of diabetic endothelial dysfunction and highlights the potential of iPSC-based models for drug discovery and personalized medicine.

Indexed as

cardiovascular diseasesdiabetes mellitusdisease modelingdrug screeningendothelial cellsinduced pluripotent stem cells

Identifiers

PMID38023728
PMCPMC10658533
OpenAlexW4386331146

What OpenQuestion holds

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LicenceCC BY
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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.