Evidence map›Paper›PMID 30846806›Full record

ArticleScientific reports2019

Application of a Flow-Based Hollow-Fiber Co-Culture System to Study Cellular Influences under Hyperglycemic Conditions.

Abdul Shukkur Ebrahim, Thomas W Carion, Eliisa Strand, Laura A Young, Haoshen Shi, Elizabeth A Berger

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

6 authors at 1 institution in 1 country.

Abdul Shukkur EbrahimDepartment of Ophthalmology, Visual & Anatomical Sciences Wayne State University School of Medicine Detroit, Detroit, MI, 48201, USA.
Thomas W CarionDepartment of Ophthalmology, Visual & Anatomical Sciences Wayne State University School of Medicine Detroit, Detroit, MI, 48201, USA.
Eliisa StrandDepartment of Ophthalmology, Visual & Anatomical Sciences Wayne State University School of Medicine Detroit, Detroit, MI, 48201, USA.ORCID 0000-0001-7348-5182
Laura A YoungDepartment of Ophthalmology, Visual & Anatomical Sciences Wayne State University School of Medicine Detroit, Detroit, MI, 48201, USA.
Haoshen ShiDepartment of Ophthalmology, Visual & Anatomical Sciences Wayne State University School of Medicine Detroit, Detroit, MI, 48201, USA.
Elizabeth A BergerDepartment of Ophthalmology, Visual & Anatomical Sciences Wayne State University School of Medicine Detroit, Detroit, MI, 48201, USA. eberger@med.wayne.edu.
Wayne State University · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
VISION RESEARCH--COREP30EY004068 · NEI · WAYNE STATE UNIVERSITY · PI LINDA D HAZLETT · 1985 to 2026
$13.2M
NCI NIH HHS P30 CA022453NEI NIH HHS P30 EY004068
6 · The paper itself

Abstract

Elucidation of the basic mechanisms underlying human disease pathogenesis depends on the findings afforded to us through in vivo and in vitro approaches. While there are inherent limitations in any model system, 2D in vitro culture systems tend to be particularly restricted due to their static nature. Here, we adapted a flow-based hollow-fiber cartridge system to better understand the cellular influences of human retinal microvascular endothelial cells and mouse-derived neutrophils under high glucose conditions similar to those observed in diabetes. Analyses by western blot and flow cytometry indicate that pro-inflammatory molecules known to be associated with the pathogenesis of diabetic retinopathy were significantly elevated following high glucose exposure, including VEGF, ICAM-1, and ROS. Changes in mitochondrial potential were also observed. Further, we demonstrate that this innovative system allows for cross-species co-culture as well as long-term culturing conditions. This in vitro modeling system not only mimics the retinal microvasculature, it also allows for the examination of cellular interactions and mechanisms that contribute to diabetic retinopathy, a visually debilitating complication of diabetes.

Indexed as

AnimalsCoculture TechniquesDiabetic RetinopathyEndothelial CellsEquipment DesignFemaleHumansHyperglycemiaIntercellular Adhesion Molecule-1Mice, Inbred C57BLNeutrophilsOxidative StressReactive Oxygen SpeciesRetinal VesselsVascular Endothelial Growth Factor AICAM1 protein, humanIntercellular Adhesion Molecule-1Reactive Oxygen SpeciesVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID30846806
PMCPMC6405855
OpenAlexW2920064297

What OpenQuestion holds

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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.