Evidence map›Paper›PMID 30590182›Full record

ArticleActa biomaterialia2019

Directing the growth and alignment of biliary epithelium within extracellular matrix hydrogels.

Phillip L Lewis, Ming Yan, Jimmy Su, Ramille N Shah

Abstract read
In one paragraph

Article in Acta biomaterialia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
  2. Review
  3. A Systematic Review on Artificial Liver for Implantation.Journal of functional biomaterials · 2026
    Review
  4. Article
  5. Article
  6. 3D bioprinting for bile duct tissue engineering: current status and prospects.Frontiers in bioengineering and biotechnology · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review
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

4 authors.

Phillip L LewisBiomedical Engineering, Northwestern University, Evanston, IL, United States; Simpson/Querrey Institute, Northwestern University, Chicago, IL, United States. Electronic address: Phillip.lewis@cchmc.org.
Ming YanBiomedical Engineering, Northwestern University, Evanston, IL, United States; Simpson/Querrey Institute, Northwestern University, Chicago, IL, United States. Electronic address: mingyan2018@u.northwestern.edu.
Jimmy SuBiomedical Engineering, Northwestern University, Evanston, IL, United States; Simpson/Querrey Institute, Northwestern University, Chicago, IL, United States. Electronic address: jimmysu2020@u.northwestern.edu.
Ramille N ShahSimpson/Querrey Institute, Northwestern University, Chicago, IL, United States; Surgery - Transplant Division, Northwestern University, Chicago, IL, United States; Materials Science and Engineering, Northwestern University, Evanston, IL, United States. Electronic address: ramille@uic.edu.

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
Multifunctional Printed Scaffolds for Enhancing Hepatocyte Viability and FunctionK01DK099454 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SHAH, RAMILLE N · 2013 to 2017
$652k
Microenvironmental Signaling Cues to Model Glomerular Endothelial Cell and Podocyte InteractionsF31DK108544 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SU, JIMMY · 2017 to 2018
$77k
NCI NIH HHS P30 CA060553NIDDK NIH HHS F31 DK108544NIDDK NIH HHS K01 DK099454NIGMS NIH HHS T32 GM008449
6 · The paper itself

Abstract

Three-dimensional (3D) printing of decellularized extracellular matrix (dECM) hydrogels is a promising technique for regenerative engineering. 3D-printing enables the reproducible and precise patterning of multiple cells and biomaterials in 3D, while dECM has high organ-specific bioactivity. However, dECM hydrogels often display poor printability on their own and necessitate additives or support materials to enable true 3D structures. In this study, we used a sacrificial material, 3D-printed Pluronic F-127, to serve as a platform into which dECM hydrogel can be incorporated to create specifically designed structures made entirely up of dECM. The effects of 3D dECM are studied in the context of engineering the intrahepatic biliary tree, an often-understudied topic in liver tissue engineering. Encapsulating biliary epithelial cells (cholangiocytes) within liver dECM has been shown to lead to the formation of complex biliary trees in vitro. By varying several aspects of the dECM structures' geometry, such as width and angle, we show that we can guide the directional formation of biliary trees. This is confirmed by computational 3D image analysis of duct alignment. This system also enables fabrication of a true multi-layer dECM structure and the formation of 3D biliary trees into which other cell types can be seeded. For example, we show that hepatocyte spheroids can be easily incorporated within this system, and that the seeding sequence influences the resulting structures after seven days in culture. STATEMENT OF SIGNIFICANCE: The field of liver tissue engineering has progressed significantly within the past several years, however engineering the intrahepatic biliary tree has remained a significant challenge. In this study, we utilize the inherent bioactivity of decellularized extracellular matrix (dECM) hydrogels and 3D-printing of a sacrificial biomaterial to create spatially defined, 3D biliary trees. The creation of patterned, 3D dECM hydrogels in the past has only been possible with additives to the gel that may stifle its bioactivity, or with rigid and permanent support structures that may present issues upon implantation. Additionally, the biological effect of 3D spatially patterned liver dECM has not been demonstrated independent of the effects of dECM bioactivity alone. This study demonstrates that sacrificial materials can be used to create pure, multi-layer dECM structures, and that strut width and angle can be changed to influence the formation and alignment of biliary trees encapsulated within. Furthermore, this strategy allows co-culture of other cells such as hepatocytes. We demonstrate that not only does this system show promise for tissue engineering the intrahepatic biliary tree, but it also aids in the study of duct formation and cell-cell interactions.

Indexed as

AnimalsBile DuctsBiliary TractCoculture TechniquesEpitheliumExtracellular MatrixFemaleHepatocytesHumansHydrogelsMicePrinting, Three-DimensionalSwineTissue ScaffoldsHydrogels3D printingBile ductDecellularizedExtracellular matrixHydrogelLiverTissue engineering

Identifiers

PMID30590182
PMCPMC6768828

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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.