Evidence map›Paper›PMID 20488537›Full record

ArticleBiomaterials2010

Cultivating hepatocytes on printed arrays of HGF and BMP7 to characterize protective effects of these growth factors during in vitro alcohol injury.

Caroline N Jones, Nazgul Tuleuova, Ji Youn Lee, Erlan Ramanculov, A Hari Reddi, Mark A Zern, Alexander Revzin

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Engineered Livers for Infectious Diseases.Cellular and molecular gastroenterology and hepatology · 2018
    Review
  8. BMP Signalling at the Crossroad of Liver Fibrosis and Regeneration.International journal of molecular sciences · 2017
    Review
  9. Harnessing endogenous signals from hepatocytes using a low volume multi-well plate.Integrative biology : quantitative biosciences from nano to macro · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Cell and tissue engineering for liver disease.Science translational medicine · 2014
    Review
  15. Local control of hepatic phenotype with growth factor-encoded surfaces.Integrative biology : quantitative biosciences from nano to macro · 2014
    Article
  16. Article
  17. Article
  18. Life on a microarray: assessing live cell functions in a microarray format.Cellular and molecular life sciences : CMLS · 2012
    Review
  19. Article
  20. Cell signals influencing hepatic fibrosis.International journal of hepatology · 2012
    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

7 authors at 2 institutions in 2 countries.

Caroline N JonesDepartment of Biomedical Engineering, University of California, Davis, CA 95616, USA.
Nazgul Tuleuova
Ji Youn Lee
Erlan Ramanculov
A Hari Reddi
Mark A Zern
Alexander Revzin
University of California, Davis · USNational Center for Biotechnology · KZ

Funding

Effects of Microengineered Interactions on Liver-Specific Gene ExpressionR21DK073901 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI REVZIN, ALEXANDER · 2006 to 2007
$395k
NIBIB NIH HHS EB010131NIDDK NIH HHS DK073901NIDDK NIH HHS R21 DK073901
6 · The paper itself

Abstract

The goal of the present study was to investigate hepato-protective effects of growth factor (GF) arrays during alcohol injury. Hepatocyte growth factor (HGF) and bone morphogenetic protein (BMP)7 were mixed with collagen (I) and robotically printed onto standard glass slides to create arrays of 500 microm diameter spots. Primary rat hepatocytes were seeded on top of the arrays forming clusters corresponding in size to the underlying protein spots. Cell arrays were then injured in culture by exposure to 100 mm ethanol for 48 h. Hepatocytes residing on GF spots were found to have less apoptosis then cells cultured on collagen-only spots. Least apoptosis (0.3% as estimated by TUNEL assay) was observed on HGF/BMP7/collagen spots whereas most apoptosis (17.3%) was seen on collagen-only arrays. Interestingly, the extent of alcohol-induced apoptosis in hepatocytes varied based on the concentration of printed GF. In addition to preventing apoptosis, printed GFs contributed to maintenance of epithelial phenotype during alcohol injury as evidenced by higher levels of E-cadherin expression in HGF-protected hepatocytes. Importantly, GF microarrays could be used to investigate heterotypic interactions in the context of liver injury. To highlight this, stellate cells - nonparenchymal liver cells involved in fibrosis - were added to hepatocytes residing on arrays of either HGF/collagen or collagen-only spots. Exposure of these cocultures to ethanol followed by RT-PCR analysis revealed that stellate cells residing alongside HGF-protected hepatocytes were significantly less activated (less fibrotic) compared to controls. Overall, our results demonstrate that GF microarray format can be used to screen anti-fibrotic and anti-apoptotic effects of growth factors as well as to investigate how signals delivered to a specific cell type modulate heterotypic cellular interactions.

Indexed as

AnimalsApoptosisBase SequenceBone Morphogenetic Protein 7Cells, CulturedDNA PrimersFemaleHepatocyte Growth FactorHepatocytesIn Situ Nick-End LabelingRatsReverse Transcriptase Polymerase Chain ReactionBone Morphogenetic Protein 7DNA PrimersHepatocyte Growth Factor

Identifiers

PMID20488537
PMCPMC2893270
OpenAlexW2134239458

What OpenQuestion holds

Textmetadata
LicenceTDM
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.