Evidence map›Paper›PMID 27159223›Full record

ArticlePloS one2016

Optimization of Liver Decellularization Maintains Extracellular Matrix Micro-Architecture and Composition Predisposing to Effective Cell Seeding.

Panagiotis Maghsoudlou, Fanourios Georgiades, Holly Smith, Anna Milan, Panicos Shangaris, Luca Urbani, Stavros P Loukogeorgakis, Benedetta Lombardi, Giuseppe Mazza, Charlotte Hagen and 8 more

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

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  18. Recent Advances in Liver Engineering With Decellularized Scaffold.Frontiers in bioengineering and biotechnology · 2022
    Review
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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

18 authors.

Panagiotis MaghsoudlouDepartment of Stem Cells and Regenerative Medicine, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London, WC1N 1EH, United Kingdom.
Fanourios GeorgiadesDepartment of Stem Cells and Regenerative Medicine, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London, WC1N 1EH, United Kingdom.
Holly SmithMRC Laboratory for Molecular Cell Biology, University College London, London, WC1E 6BT, United Kingdom.
Anna MilanDepartment of Stem Cells and Regenerative Medicine, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London, WC1N 1EH, United Kingdom.
Panicos ShangarisDepartment of Stem Cells and Regenerative Medicine, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London, WC1N 1EH, United Kingdom.
Luca UrbaniDepartment of Stem Cells and Regenerative Medicine, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London, WC1N 1EH, United Kingdom.
Stavros P LoukogeorgakisDepartment of Stem Cells and Regenerative Medicine, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London, WC1N 1EH, United Kingdom.
Benedetta LombardiLondon Center for Nephrology, University College London, London, WC1N 1EH, United Kingdom.
Giuseppe MazzaInstitute for Liver and Digestive Health, University College London, London, WC1N 1EH, United Kingdom.
Charlotte HagenDepartment of Medical Physics & Bioengineering, University College London, London, WC1N 1EH, United Kingdom.
Neil J SebireDepartment of Histopathology, UCL Institute of Child Health and Great Ormond Street Hospital, London, WC1N 1EH, United Kingdom.
Mark TurmaineDivision of Bioscience, University College London, London, WC1N 1EH, United Kingdom.
Simon EatonDepartment of Stem Cells and Regenerative Medicine, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London, WC1N 1EH, United Kingdom.
Alessandro OlivoDepartment of Medical Physics & Bioengineering, University College London, London, WC1N 1EH, United Kingdom.
Jasminka Godovac-ZimmermannLondon Center for Nephrology, University College London, London, WC1N 1EH, United Kingdom.
Massimo PinzaniInstitute for Liver and Digestive Health, University College London, London, WC1N 1EH, United Kingdom.
Paul GissenMRC Laboratory for Molecular Cell Biology, University College London, London, WC1E 6BT, United Kingdom.
Paolo De CoppiDepartment of Stem Cells and Regenerative Medicine, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London, WC1N 1EH, United Kingdom.

Funding

Department of Health RP_2014-04-046European Research Council 337057Medical Research CouncilWellcome TrustWellcome Trust WT095662MA
6 · The paper itself

Abstract

Hepatic tissue engineering using decellularized scaffolds is a potential therapeutic alternative to conventional transplantation. However, scaffolds are usually obtained using decellularization protocols that destroy the extracellular matrix (ECM) and hamper clinical translation. We aim to develop a decellularization technique that reliably maintains hepatic microarchitecture and ECM components. Isolated rat livers were decellularized by detergent-enzymatic technique with (EDTA-DET) or without EDTA (DET). Histology, DNA quantification and proteomics confirmed decellularization with further DNA reduction with the addition of EDTA. Quantification, histology, immunostaining, and proteomics demonstrated preservation of extracellular matrix components in both scaffolds with a higher amount of collagen and glycosaminoglycans in the EDTA-DET scaffold. Scanning electron microscopy and X-ray phase contrast imaging showed microarchitecture preservation, with EDTA-DET scaffolds more tightly packed. DET scaffold seeding with a hepatocellular cell line demonstrated complete repopulation in 14 days, with cells proliferating at that time. Decellularization using DET preserves microarchitecture and extracellular matrix components whilst allowing for cell growth for up to 14 days. Addition of EDTA creates a denser, more compact matrix. Transplantation of the scaffolds and scaling up of the methodology are the next steps for successful hepatic tissue engineering.

Indexed as

LiverTissue ScaffoldsAnimalsChromatography, LiquidHep G2 CellsHumansMicroscopy, Electron, ScanningRatsTandem Mass Spectrometry

Identifiers

PMID27159223
PMCPMC4861300

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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.