Evidence map›Paper›PMID 34786888›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Directing Cholangiocyte Morphogenesis in Natural Biomaterial Scaffolds.

Quinton Smith, Jennifer Bays, Linqing Li, Haniyah Shareef, Christopher S Chen, Sangeeta N Bhatia

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. 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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. A 3D In Vitro Model of the Human Hepatobiliary Junction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Review
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Quinton SmithHoward Hughes Medical Institute, Chevy Chase, MD, 20815, USA.ORCID 0000-0001-7079-1176
Jennifer BaysDepartment of Bioengineering, Boston University, Boston, MA, 02215, USA.
Linqing LiDepartment of Bioengineering, Boston University, Boston, MA, 02215, USA.
Haniyah ShareefDavid H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02142, USA.
Christopher S ChenDepartment of Bioengineering, Boston University, Boston, MA, 02215, USA.
Sangeeta N BhatiaHoward Hughes Medical Institute, Chevy Chase, MD, 20815, USA.ORCID 0000-0001-6174-3391
Boston University · USHoward Hughes Medical Institute · USMassachusetts Institute of Technology · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Paula T Hammond · 1985 to 2026
$93.9M
Engineering Multicellular Tissue Structure, Function, and VascularizationR01EB008396 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI BHATIA, SANGEETA N., CHEN, CHRISTOPHER S · 2009 to 2018
$5.8M
Organ Design and Engineering Training Program (ODET Program)T32EB016652 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT · 2014 to 2023
$3.5M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA014051NIBIB NIH HHS R01 EB008396NIBIB NIH HHS T32 EB016652NIH HHS EB008396
6 · The paper itself

Abstract

Patients with Alagille syndrome carry monogenic mutations in the Notch signaling pathway and face complications such as jaundice and cholestasis. Given the presence of intrahepatic ductopenia in these patients, Notch2 receptor signaling is implicated in driving normal biliary development and downstream branching morphogenesis. As a result, in vitro model systems of liver epithelium are needed to further mechanistic insight of biliary tissue assembly. Here, primary human intrahepatic cholangiocytes as a candidate population for such a platform are systematically evaluated, and conditions that direct their branching morphogenesis are described. It is found that extracellular matrix presentation, coupled with mitogen stimulation, promotes biliary branching in a Notch-dependent manner. These results demonstrate the utility of using 3D scaffolds for mechanistic investigation of cholangiocyte branching and provide a gateway to integrate biliary architecture in additional in vitro models of liver tissue.

Indexed as

Tissue ScaffoldsAdultAlagille SyndromeBiliary TractBiocompatible MaterialsCells, CulturedEpithelial CellsHumansLiverMorphogenesisOrganoidsSignal TransductionBiocompatible Materialsbiomaterials, cholangiocyte morphogenesislivermicrofluidicsmorphogenesis

Identifiers

PMID34786888
PMCPMC8787431
OpenAlexW3214374810

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.