Evidence map›Paper›PMID 19302848›Full record

ArticleJournal of pediatric surgery2009

Cholangiocyte secretion of chemokines in experimental biliary atresia.

Mubeen Jafri, Bryan Donnelly, Alex Bondoc, Steven Allen, Greg Tiao

Open access · greenAbstract read
In one paragraph

Article in Journal of pediatric surgery, 2009. 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
3.5field-weighted citation impact, top 8% 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, 35 citations in OpenAlex.

  1. Article
  2. Deletion of Interferon Lambda Receptor Elucidates Susceptibility to the Murine Model of Biliary Atresia.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2023
    Article
  3. Article
  4. Review
  5. Cell-specific regulatory effects of CXCR2 on cholestatic liver injury.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
  6. Article
  7. Functional and structural features of cholangiocytes in health and disease.Cellular and molecular gastroenterology and hepatology · 2015
    Article
  8. Review
  9. MicroRNAs and benign biliary tract diseases.Seminars in liver disease · 2015
    Review
  10. Article
  11. Article
  12. Article
  13. Aetiology of biliary atresia: what is actually known?Orphanet journal of rare diseases · 2013
    Review
  14. Article
  15. Advances in cholangiocyte immunobiology.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Mubeen JafriDepartment of Pediatric and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Bryan Donnelly
Alex Bondoc
Steven Allen
Greg Tiao
Cincinnati Children's Hospital Medical Center · US

Funding

Pathogenic Mechanisms of Virus Induced Biliary AtresiaK08DK072858 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI TIAO, GREGORY M · 2005 to 2009
$630k
NIDDK NIH HHS K08 DK072858
6 · The paper itself

Abstract

unlabelledBiliary atresia (BA) is a disease of the newborn that results in obstruction of the biliary tree. The cause of BA remains unknown; however, recent studies using the murine model of biliary atresia have found that rotavirus infection of the biliary epithelial cell (cholangiocyte) triggers an inflammatory response. We hypothesized that rotavirus infection of cholangiocytes results in the release of chemokines, important mediators of the host immune response.

methodsIn vivo, Balb/c pups were injected with rhesus rotavirus (RRV) or saline, and, their extrahepatic bile ducts were microdissected 2, 5, 7, and 14 days after injection. Next, an immortalized cholangiocyte cell line (mCl) was incubated with RRV or serum-free media. Qualitative and quantitative chemokine assessment was performed using enzyme-linked immunosorbent assay, polymerase chain reaction, and immunohistochemistry.

resultsIn vivo, increased levels of the chemokines macrophage inflammatory protein 2, monocyte chemotactic protein 1, KC and Regulated upon Activation, Normal T Expressed and Secreted were found in RRV-infected murine bile ducts. In vitro, infected mCl cells produced increasing amounts of these same chemokines in relation to dose and time.

conclusionThese novel results suggest that chemokine expression by RRV-infected cholangiocytes may trigger a host inflammatory process that causes bile duct obstruction. Understanding how viral infection initiates this response may shed light on the pathogenesis of biliary atresia.

Indexed as

AnimalsAnimals, NewbornBile Ducts, ExtrahepaticBiliary AtresiaCell LineChemokine CCL17Chemokine CCL2Chemokine CCL5Chemokine CXCL2ChemokinesDisease Models, AnimalDisease ProgressionImmunohistochemistryMiceMice, Inbred BALB CRotavirusCcl17 protein, mouseCcl2 protein, mouseChemokine CCL17Chemokine CCL2Chemokine CCL5Chemokine CXCL2ChemokinesCxcl2 protein, mouse

Identifiers

PMID19302848
PMCPMC2730110
OpenAlexW2056692303

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.