Evidence map›Paper›PMID 28717194›Full record

ArticleScientific reports2017

Rapid production of human liver scaffolds for functional tissue engineering by high shear stress oscillation-decellularization.

Giuseppe Mazza, Walid Al-Akkad, Andrea Telese, Lisa Longato, Luca Urbani, Benjamin Robinson, Andrew Hall, Kenny Kong, Luca Frenguelli, Giusi Marrone and 14 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
10.7field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Protective effects ofCytotechnology · 2025
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  10. Mechanobiology of portal hypertension.JHEP reports : innovation in hepatology · 2023
    Review
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  13. Tissue CD14Nature · 2023
    Article
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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

24 authors at 6 institutions in 2 countries.

Giuseppe MazzaUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK. giuseppe.mazza.12@ucl.ac.uk.
Walid Al-AkkadUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
Andrea TeleseUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
Lisa LongatoUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
Luca UrbaniStem Cells and Regenerative Medicine Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute for Child Health. University College London, London, UK.
Benjamin RobinsonDepartment of Bioengineering, Cellular and Molecular Biomechanics. Imperial College, London, UK.
Andrew HallUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
Kenny KongSchool of Physics and Astronomy, University of Nottingham, Nottingham, UK.
Luca FrenguelliUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
Giusi MarroneUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.ORCID 0000-0001-9029-7378
Oliver WillacyUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
Mohsen ShaeriCN Bio Innovations Limited. BioPark Hertfordshire, Broadwater Road, Welwyn Garden City, Hertfordshire, UK.
Alan BurnsStem Cells and Regenerative Medicine Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute for Child Health. University College London, London, UK.
Massimo MalagoUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
Janet GilbertsonWolfson Drug Discovery Unit, Centre for Amyloidosis and Acute Phase Proteins, Royal Free Hospital. University College London, London, UK.
Nigel RendellWolfson Drug Discovery Unit, Centre for Amyloidosis and Acute Phase Proteins, Royal Free Hospital. University College London, London, UK.
Kevin MooreUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
David HughesCN Bio Innovations Limited. BioPark Hertfordshire, Broadwater Road, Welwyn Garden City, Hertfordshire, UK.
Ioan NotingherSchool of Physics and Astronomy, University of Nottingham, Nottingham, UK.
Gavin JellCenter for Nanotechnology and Regenerative Medicine, Division of Surgery and Interventional Science. University College London, London, UK.
Armando Del Rio HernandezDepartment of Bioengineering, Cellular and Molecular Biomechanics. Imperial College, London, UK.
Paolo De CoppiStem Cells and Regenerative Medicine Section, Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute for Child Health. University College London, London, UK.
Krista RomboutsUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
Massimo PinzaniUCL Institute for Liver and Digestive Health, Royal Free Hospital. University College London, London, UK.
The Royal Free Hospital · GBGreat Ormond Street Hospital · GBCN Bio Innovations (United Kingdom) · GBImperial College London · GBUniversity of Nottingham · GBLondon Centre for Nanotechnology · GB

Funding

Department of Health RP_2014-04-046European Research Council 282051Medical Research CouncilWellcome Trust
6 · The paper itself

Abstract

The development of human liver scaffolds retaining their 3-dimensional structure and extra-cellular matrix (ECM) composition is essential for the advancement of liver tissue engineering. We report the design and validation of a new methodology for the rapid and accurate production of human acellular liver tissue cubes (ALTCs) using normal liver tissue unsuitable for transplantation. The application of high shear stress is a key methodological determinant accelerating the process of tissue decellularization while maintaining ECM protein composition, 3D-architecture and physico-chemical properties of the native tissue. ALTCs were engineered with human parenchymal and non-parenchymal liver cell lines (HepG2 and LX2 cells, respectively), human umbilical vein endothelial cells (HUVEC), as well as primary human hepatocytes and hepatic stellate cells. Both parenchymal and non-parenchymal liver cells grown in ALTCs exhibited markedly different gene expression when compared to standard 2D cell cultures. Remarkably, HUVEC cells naturally migrated in the ECM scaffold and spontaneously repopulated the lining of decellularized vessels. The metabolic function and protein synthesis of engineered liver scaffolds with human primary hepatocytes reseeded under dynamic conditions were maintained. These results provide a solid basis for the establishment of effective protocols aimed at recreating human liver tissue in vitro.

Indexed as

Tissue EngineeringCell Culture TechniquesCell MovementCells, CulturedExtracellular MatrixHepatic Stellate CellsHepatocytesHumansHuman Umbilical Vein Endothelial CellsMicroscopy, Electron, ScanningShear StrengthTissue Scaffolds

Identifiers

PMID28717194
PMCPMC5514140
OpenAlexW2736239655

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.