Evidence map›Paper›PMID 28029279›Full record

ArticleOrganogenesis2017

Recellularization via the bile duct supports functional allogenic and xenogenic cell growth on a decellularized rat liver scaffold.

Wessam Hassanein, Mehmet C Uluer, John Langford, Jhade D Woodall, Arielle Cimeno, Urmil Dhru, Avraham Werdesheim, Joshua Harrison, Carlos Rivera-Pratt, Stephen Klepfer and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Organogenesis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Rat liver ECM incorporated into electrospun polycaprolactone scaffolds as a platform for hepatocyte culture.Journal of biomedical materials research. Part B, Applied biomaterials · 2022
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. In Vivo Performance of Decellularized Vascular Grafts: A Review Article.International journal of molecular sciences · 2018
    Review
  15. 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

18 authors at 1 institution in 1 country.

Wessam Hassaneina University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Mehmet C Uluera University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
John Langforda University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Jhade D Woodalla University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Arielle Cimenoa University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Urmil Dhrua University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Avraham Werdesheima University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Joshua Harrisona University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Carlos Rivera-Pratta University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Stephen Klepfera University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Ali Khalifeha University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Bryan Buckinghama University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Philip S Brazioa University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Dawn Parsella University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Charlie Klassena University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
Cinthia Drachenbergb University of Maryland School of Medicine , Department of Pathology , Baltimore , MD , USA.
Rolf N Bartha University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
John C LaMattinaa University of Maryland School of Medicine, Department of Surgery , Division of Transplantation , Baltimore , MD , USA.
University of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent years have seen a proliferation of methods leading to successful organ decellularization. In this experiment we examine the feasibility of a decellularized liver construct to support growth of functional multilineage cells. Bio-chamber systems were used to perfuse adult rat livers with 0.1% SDS for 24 hours yielding decellularized liver scaffolds. Initially, we recellularized liver scaffolds using a human tumor cell line (HepG2, introduced via the bile duct). Subsequent studies were performed using either human tumor cells co-cultured with human umbilical vein endothelial cells (HUVECs, introduced via the portal vein) or rat neonatal cell slurry (introduced via the bile duct). Bio-chambers were used to circulate oxygenated growth medium via the portal vein at 37C for 5-7 days. Human HepG2 cells grew readily on the scaffold (n = 20). HepG2 cells co-cultured with HUVECs demonstrated viable human endothelial lining with concurrent hepatocyte growth (n = 10). In the series of neonatal cell slurry infusion (n = 10), distinct foci of neonatal hepatocytes were observed to repopulate the parenchyma of the scaffold. The presence of cholangiocytes was verified by CK-7 positivity. Quantitative albumin measurement from the grafts showed increasing albumin levels after seven days of perfusion. Graft albumin production was higher than that observed in traditional cell culture. This data shows that rat liver scaffolds support human cell ingrowth. The scaffold likewise supported the engraftment and survival of neonatal rat liver cell slurry. Recellularization of liver scaffolds thus presents a promising model for functional liver engineering.

Indexed as

AlbuminsAnimalsAnimals, NewbornBile DuctsCell CompartmentationCell LineageCell ProliferationCell TrackingDNAHep G2 CellsHumansHuman Umbilical Vein Endothelial CellsLiverMaleRats, WistarReproducibility of ResultsAlbuminsDNAbioengineeringdecellularizationliverorgan scaffoldratrecellularization

Identifiers

PMID28029279
PMCPMC5323036
OpenAlexW2561796813

What OpenQuestion holds

Textmetadata
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.