Evidence map›Paper›PMID 41973609›Full record

ReviewPhysiological reviews2026

Cholangiocyte biology in primary sclerosing cholangitis and other cholangiopathies: pathogenesis, clinical insights, and experimental tools.

Nidhi Jalan-Sakrikar, Abid A Anwar, Ahmad Ali, Navine Nasser-Ghodsi, Antonia Felzen, Robert C Huebert, Nicholas F LaRusso, Steven P O'Hara

Abstract readReview
In one paragraph

Review in Physiological reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Nidhi Jalan-SakrikarDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0001-6795-0121
Abid A AnwarDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, United States.
Ahmad AliDivision of Gastroenterology and Hepatology, University of Missouri School of Medicine, Columbia, Missouri, United States.
Navine Nasser-GhodsiDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, United States.
Antonia FelzenDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, United States.
Robert C HuebertDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, United States.
Nicholas F LaRussoDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, United States.ORCID 0000-0003-3266-0831
Steven P O'HaraDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, United States.

Funding

Institutional Career Development CoreKL2TR002379 · NCATS · MAYO CLINIC ROCHESTER · PI NILUFER ERTEKIN-TANER · 2017 to 2026
$14.9M
Pathophysiology of Biliary DiseaseR01DK057993 · NIDDK · MAYO CLINIC ROCHESTER · PI LARUSSO, NICHOLAS F., O'HARA, STEVEN P · 2001 to 2025
$7.1M
Molecular Mechanisms of Cholestatic FibrogenesisR01DK117861 · NIDDK · MAYO CLINIC ROCHESTER · PI Robert Christian Huebert · 2019 to 2026
$2.8M
American Association for the Study of Liver Diseases (AASLD)HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK117861HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) DK57993MC | Center for Clinical and Translational Science, Mayo Clinic (CCaTS) K2R AwardNCATS NIH HHS KL2 TR002379NIDDK NIH HHS R01 DK057993NIDDK NIH HHS R01 DK117861PSC Partners Seeking a Cure (PSC)
6 · The paper itself

Abstract

Cholangiocytes are specialized epithelial cells that line the intrahepatic and extrahepatic biliary tree and play a critical role in bile modification, liver homeostasis, and response to injury. Cholangiocytes exhibit notable heterogeneity and plasticity, and their dysfunction is central to a spectrum of diseases targeting the bile ducts, collectively called cholangiopathies. These disorders include genetic, infectious, immune-mediated, and malignant diseases, with primary sclerosing cholangitis (PSC) representing one of the most complex and enigmatic of these disorders. PSC is a progressive, fibro-inflammatory disease of the bile ducts that is closely linked to inflammatory bowel disease, carries a heightened risk of cancer, and lacks any approved therapies. This review explores the biology of cholangiocytes, including their development, functional plasticity, and roles in secretion, absorption, and cellular signaling. We provide a detailed examination of cholangiopathies, particularly PSC, a complex cholangiopathy characterized by a paradoxical state of cholangiocyte senescence and hyperproliferation. We describe how immune cell dysfunction, the gut microbiome, genetic predispositions, and environmental factors converge to mediate PSC pathogenesis. We revisit the foundational technologies that empowered early discoveries and shaped the field as we know it today. We also explore how newer techniques such as organoid cultures, single-cell transcriptomics, epigenomics, and spatialomics have transformed our modern understanding of biliary pathophysiology. Finally, we provide an overview of existing rodent models of cholangiopathies and discuss their relevance to human disease. PSC remains therapeutically unaddressed, and thus ongoing multidisciplinary efforts are essential to developing targeted interventions. This review serves as a comprehensive resource for researchers and clinicians navigating the rapidly evolving landscape of cholangiocyte-centered liver disease research.

Indexed as

Bile DuctsCholangitis, SclerosingEpithelial CellsAnimalsHumansbiliary cellsductular reactionsenescence

Identifiers

PMID41973609
PMCPMC13148226

What Socratic holds

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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 Socratic graph.