Evidence map›Paper›PMID 25950942›Full record

ArticleBiosensors & bioelectronics2015

Real-time quantitative monitoring of hiPSC-based model of macular degeneration on Electric Cell-substrate Impedance Sensing microelectrodes.

W Gamal, S Borooah, S Smith, I Underwood, V Srsen, S Chandran, P O Bagnaninchi, B Dhillon

Open access · hybridAbstract read
In one paragraph

Article in Biosensors & bioelectronics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 39 citations in OpenAlex.

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  12. Impedance-based cellular assays for regenerative medicine.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  13. Engineering and monitoring cellular barrier models.Journal of biological engineering · 2018
    Review
  14. 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

8 authors at 3 institutions in 1 country.

W GamalInstitute for Bioengineering, School of Engineering, The University of Edinburgh, EH9 3DW, United Kingdom.
S BorooahMRC Centre for Regenerative Medicine, The University of Edinburgh, EH16 4UU, United Kingdom; Centre for Clinical Brain Sciences, The University of Edinburgh, EH16 4SB, United Kingdom; Euan MacDonald Centre for MND Research, The University of Edinburgh, EH16 4SB, United Kingdom; Centre for Neuroregeneration, The University of Edinburgh, EH16 4SB, United Kingdom; The Anne Rowling Regenerative Neurology Clinic, The University of Edinburgh, EH16 4SB, United Kingdom.
S SmithInstitute for Bioengineering, School of Engineering, The University of Edinburgh, EH9 3DW, United Kingdom.
I UnderwoodInstitute for Integrated Micro and Nano Systems, School of Engineering, The University of Edinburgh, EH9 3JF, United Kingdom.
V SrsenInstitute for Bioengineering, School of Engineering, The University of Edinburgh, EH9 3DW, United Kingdom.
S ChandranMRC Centre for Regenerative Medicine, The University of Edinburgh, EH16 4UU, United Kingdom; Centre for Clinical Brain Sciences, The University of Edinburgh, EH16 4SB, United Kingdom; Euan MacDonald Centre for MND Research, The University of Edinburgh, EH16 4SB, United Kingdom; Centre for Neuroregeneration, The University of Edinburgh, EH16 4SB, United Kingdom; The Anne Rowling Regenerative Neurology Clinic, The University of Edinburgh, EH16 4SB, United Kingdom.
P O BagnaninchiMRC Centre for Regenerative Medicine, The University of Edinburgh, EH16 4UU, United Kingdom. Electronic address: Pierre.Bagnaninchi@ed.ac.uk.
B DhillonCentre for Clinical Brain Sciences, The University of Edinburgh, EH16 4SB, United Kingdom; The Anne Rowling Regenerative Neurology Clinic, The University of Edinburgh, EH16 4SB, United Kingdom; School of Clinical Sciences, The University of Edinburgh, EH16 4SB, United Kingdom.
University of Edinburgh · GBMott MacDonald (United Kingdom) · GBMRC Centre for Regenerative Medicine · GB

Funding

Wellcome TrustWellcome Trust R42141
6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is the leading cause of blindness in the developed world. Humanized disease models are required to develop new therapies for currently incurable forms of AMD. In this work, a tissue-on-a-chip approach was developed through combining human induced pluripotent stem cells, Electric Cell-substrate Impedance Sensing (ECIS) and reproducible electrical wounding assays to model and quantitatively study AMD. Retinal Pigment Epithelium (RPE) cells generated from a patient with an inherited macular degeneration and from an unaffected sibling were used to test the model platform on which a reproducible electrical wounding assay was conducted to model RPE damage. First, a robust and reproducible real-time quantitative monitoring over a 25-day period demonstrated the establishment and maturation of RPE layers on the microelectrode arrays. A spatially controlled RPE layer damage that mimicked cell loss in AMD disease was then initiated. Post recovery, significant differences (P < 0.01) in migration rates were found between case (8.6 ± 0.46 μm/h) and control cell lines (10.69 ± 0.21 μm/h). Quantitative data analysis suggested this was achieved due to lower cell-substrate adhesion in the control cell line. The ECIS cell-substrate adhesion parameter (α) was found to be 7.8 ± 0.28 Ω(1/2)cm for the case cell line and 6.5 ± 0.15 Ω(1/2)cm for the control. These findings were confirmed using cell adhesion biochemical assays. The developed disease model-on-a-chip is a powerful platform for translational studies with considerable potential to investigate novel therapies by enabling real-time, quantitative and reproducible patient-specific RPE cell repair studies.

Indexed as

MicroelectrodesBiological AssayCell MovementCells, CulturedComputer SystemsDielectric SpectroscopyEquipment DesignEquipment Failure AnalysisHumansMacular DegenerationReproducibility of ResultsRetinal Pigment EpitheliumSensitivity and SpecificityTissue Array AnalysisDisease modelHuman induced pluripotent stem cellsImpedance sensingMacular degenerationTissue-on-a-chipWound healing

Identifiers

PMID25950942
PMCPMC4456427
OpenAlexW1973719263

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.