Evidence map›Paper›PMID 31521820›Full record

ArticleBiochimica et biophysica acta. Molecular basis of disease2019

Downregulation of hepatic stem cell factor by Vivo-Morpholino treatment inhibits mast cell migration and decreases biliary damage/senescence and liver fibrosis in Mdr2

Vik Meadows, Lindsey Kennedy, Laura Hargrove, Jennifer Demieville, Fanyin Meng, Shohaib Virani, Evan Reinhart, Konstantina Kyritsi, Pietro Invernizzi, Zhihong Yang and 4 more

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta. Molecular basis of disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Overview of Innate Immune Cell Landscape in Liver Aging.International journal of molecular sciences · 2023
    Review
  7. Hepatic inflammatory responses in liver fibrosis.Nature reviews. Gastroenterology & hepatology · 2023
    Review
  8. Review
  9. Loss of apical sodium bile acid transporter alters bile acid circulation and reduces biliary damage in cholangitis.American journal of physiology. Gastrointestinal and liver physiology · 2023
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Role of Immune Cells in Biliary Repair.Frontiers in immunology · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  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

14 authors at 4 institutions in 2 countries.

Vik MeadowsResearch, Central Texas Veterans Health Care System, United States of America; Department of Medical Physiology, Texas A&M University College of Medicine, United States of America.
Lindsey KennedyDepartment of Medical Physiology, Texas A&M University College of Medicine, United States of America.
Laura HargroveDepartment of Medical Physiology, Texas A&M University College of Medicine, United States of America.
Jennifer DemievilleResearch, Central Texas Veterans Health Care System, United States of America.
Fanyin MengResearch, Central Texas Veterans Health Care System, United States of America.
Shohaib ViraniDepartment of Medical Physiology, Texas A&M University College of Medicine, United States of America.
Evan ReinhartDepartment of Medical Physiology, Texas A&M University College of Medicine, United States of America.
Konstantina KyritsiDepartment of Medical Physiology, Texas A&M University College of Medicine, United States of America.
Pietro InvernizziHumanitas Clinical and Research Center, Rozzano, Milan, Italy.
Zhihong YangRichard L. Roudebush VA Medical Center, Division of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, United States of America.
Nan WuRichard L. Roudebush VA Medical Center, Division of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, United States of America.
Suthat LiangpunsakulRichard L. Roudebush VA Medical Center, Division of Gastroenterology and Hepatology, Department of Medicine, Indiana University School of Medicine, United States of America.
Gianfranco AlpiniResearch, Central Texas Veterans Health Care System, United States of America; Department of Medical Physiology, Texas A&M University College of Medicine, United States of America.
Heather FrancisResearch, Central Texas Veterans Health Care System, United States of America; Department of Medical Physiology, Texas A&M University College of Medicine, United States of America. Electronic address: heafranc@iu.edu.
Central Texas Veterans Health Care System · USTexas A&M University · USRichard L. Roudebush VA Medical Center · USHumanitas University · IT

Funding

The Paracrine Regulation of Mast Cells During Biliary/Cholangiocyte Repair and DamageR01DK108959 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI FRANCIS, HEATHER L · 2016 to 2024
$2.5M
Mechanisms of mast cell/cholangiocyte regulation of non-alcoholic fatty liver disease progressionR01DK119421 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI FRANCIS, HEATHER L · 2019 to 2022
$1.4M
Autocrine/Paracrine Regulation of Intrahepatic Bile Duct GrowthI01BX000574 · VA · RLR VA MEDICAL CENTER · PI ALPINI, GIANFRANCO D · 2009 to 2022
–
Functional characters of non-coding RNAs in alcoholic liver injuryI01BX001724 · VA · RLR VA MEDICAL CENTER · PI MENG, FANYIN · 2012 to 2024
–
Mechanisms of synergistic regulation of biliary inflammation and fibrosisI01BX003031 · VA · RLR VA MEDICAL CENTER · PI FRANCIS, HEATHER L · 2016 to 2023
–
BLR&D Research Career Scientist AwardIK6BX004601 · VA · RLR VA MEDICAL CENTER · PI ALPINI, GIANFRANCO D · 2019 to 2025
–
BLRD VA I01 BX000574BLRD VA I01 BX001724BLRD VA I01 BX003031BLRD VA IK6 BX004601NIDDK NIH HHS R01 DK108959NIDDK NIH HHS R01 DK119421
6 · The paper itself

Abstract

Primary sclerosing cholangitis (PSC) is characterized by increased mast cell (MC) infiltration, biliary damage and hepatic fibrosis. Cholangiocytes secrete stem cell factor (SCF), which is a chemoattractant for c-kit expressed on MCs. We aimed to determine if blocking SCF inhibits MC migration, biliary damage and hepatic fibrosis.

methodsFVB/NJ and Mdr2

resultsBiliary SCF expression and SCF serum levels increase in human PSC. Cholangiocytes, but not hepatocytes, from SCF Mismatch Mdr2

conclusionCholangiocytes secrete increased levels of SCF inducing MC migration, contributing to biliary damage/hepatic fibrosis. Targeting MC infiltration may be an option to ameliorate PSC progression.

Indexed as

AnimalsATP-Binding Cassette Sub-Family B Member 4ATP Binding Cassette Transporter, Subfamily BBiliary TractCell MovementCellular SenescenceCholangitis, SclerosingDown-RegulationFemaleGene DeletionHumansLiver CirrhosisMaleMast CellsMiceMorpholinosATP-Binding Cassette Sub-Family B Member 4ATP Binding Cassette Transporter, Subfamily BMorpholinosStem Cell FactorFibrosisMast cellsMigrationPSCStem cell factor

Identifiers

PMID31521820
PMCPMC6878979
OpenAlexW2972401327

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.