Evidence map›Paper›PMID 30111800›Full record

ArticleScientific reports2018

Complex bile duct network formation within liver decellularized extracellular matrix hydrogels.

Phillip L Lewis, Jimmy Su, Ming Yan, Fanyin Meng, Shannon S Glaser, Gianfranco D Alpini, Richard M Green, Beatriz Sosa-Pineda, Ramille N Shah

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Article
  3. A Systematic Review on Artificial Liver for Implantation.Journal of functional biomaterials · 2026
    Review
  4. Next-Generation Hydrogels for Biliary Organoid Engineering.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  5. A Tissue Engineering's Guide to Biomimicry.Macromolecular bioscience · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Phillip L LewisBiomedical Engineering, Northwestern University, Evanston, IL, USA.
Jimmy SuBiomedical Engineering, Northwestern University, Evanston, IL, USA.ORCID 0000-0002-7088-0176
Ming YanBiomedical Engineering, Northwestern University, Evanston, IL, USA.
Fanyin MengResearch Central Texas Veterans Health Care System, Temple, TX, USA.
Shannon S GlaserResearch Central Texas Veterans Health Care System, Temple, TX, USA.
Gianfranco D AlpiniResearch Central Texas Veterans Health Care System, Temple, TX, USA.
Richard M GreenDivision of Gastroenterology and Hepatology, Northwestern University, Chicago, IL, USA.
Beatriz Sosa-PinedaNephrology, Northwestern University, Chicago, IL, USA.
Ramille N ShahSimpson Querrey Institute, Northwestern University, Chicago, IL, USA. ramilleshah@northwestern.edu.
Northwestern University · USTemple College · USCentral Texas Veterans Health Care System · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Developing Capacity to Evaluate Training Programs via Development of Human, Institutional and Social CapitalT32GM008449 · NIGMS · NORTHWESTERN UNIVERSITY · PI LEONARD, JOSHUA NATHANIEL · 1993 to 2023
$7.8M
Role of Sensory Neuropeptides in the Regulation of Biliary FunctionR01DK076898 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2008 to 2016
$1.8M
The Role of Stem Cell Derived Microvesicles in Cholestatic Liver InjuryR01DK107310 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2015 to 2019
$1.7M
Regulation of biliary growth and fibrosis by melatoninR01DK115184 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ALPINI, GIANFRANCO D, GLASER, SHANNON STROUD · 2017 to 2020
$1.2M
Multifunctional Printed Scaffolds for Enhancing Hepatocyte Viability and FunctionK01DK099454 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SHAH, RAMILLE N · 2013 to 2017
$652k
FACSAria SORP Cell SorterS10OD011996 · OD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GOOLSBY, CHARLES L. · 2012 to 2012
$482k
Microenvironmental Signaling Cues to Model Glomerular Endothelial Cell and Podocyte InteractionsF31DK108544 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SU, JIMMY · 2017 to 2018
$77k
Autocrine/Paracrine Regulation of Intrahepatic Bile Duct GrowthI01BX000574 · VA · RLR VA MEDICAL CENTER · PI ALPINI, GIANFRANCO D · 2009 to 2022
–
Role of Mechanosensitive Receptors During Biliary Proliferation and FibrosisI01BX002192 · VA · OLIN TEAGUE VETERANS CENTER · PI GLASER, SHANNON STROUD · 2014 to 2018
–
Functional characters of non-coding RNAs in alcoholic liver injuryI01BX001724 · VA · RLR VA MEDICAL CENTER · PI MENG, FANYIN · 2012 to 2024
–
BLRD VA I01 BX000574BLRD VA I01 BX001724BLRD VA I01 BX002192NCI NIH HHS P30 CA060553NIDDK NIH HHS F31 DK108544NIDDK NIH HHS K01 DK099454NIDDK NIH HHS R01 DK076898NIDDK NIH HHS R01 DK107310NIDDK NIH HHS R01 DK115184NIGMS NIH HHS T32 GM008449NIH HHS S10 OD011996PSC Partners Seeking a Cure (PSC Partners) 7280909288FFU.S. Department of Veterans Affairs (VA) 1I01BX001724U.S. Department of Veterans Affairs (VA) 5I01BX000574U.S. Department of Veterans Affairs (VA) 5I01BX002192
6 · The paper itself

Abstract

The biliary tree is an essential component of transplantable human liver tissue. Despite recent advances in liver tissue engineering, attempts at re-creating the intrahepatic biliary tree have not progressed significantly. The finer branches of the biliary tree are structurally and functionally complex and heterogeneous and require harnessing innate developmental processes for their regrowth. Here we demonstrate the ability of decellularized liver extracellular matrix (dECM) hydrogels to induce the in vitro formation of complex biliary networks using encapsulated immortalized mouse small biliary epithelial cells (cholangiocytes). This phenomenon is not observed using immortalized mouse large cholangiocytes, or with purified collagen 1 gels or Matrigel. We also show phenotypic stability via immunostaining for specific cholangiocyte markers. Moreover, tight junction formation and maturation was observed to occur between cholangiocytes, exhibiting polarization and transporter activity. To better define the mechanism of duct formation, we utilized three fluorescently labeled, but otherwise identical populations of cholangiocytes. The cells, in a proximity dependent manner, either branch out clonally, radiating from a single nucleation point, or assemble into multi-colored structures arising from separate populations. These findings present liver dECM as a promising biomaterial for intrahepatic bile duct tissue engineering and as a tool to study duct remodeling in vitro.

Indexed as

AnimalsBile DuctsBile Ducts, IntrahepaticBiliary TractCell LineEpithelial CellsExtracellular MatrixFemaleHydrogelsLiverMiceSwineHydrogels

Identifiers

PMID30111800
PMCPMC6093899
OpenAlexW2886315925

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.