Evidence map›Paper›PMID 24045942›Full record

ArticleThe Journal of biological chemistry2013

Role of Janus kinase 3 in mucosal differentiation and predisposition to colitis.

Jayshree Mishra, Raj K Verma, Gianfranco Alpini, Fanyin Meng, Narendra Kumar

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.8field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Mucosal implications of oral Jak3-targeted drugs in COVID patients.Molecular medicine (Cambridge, Mass.) · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. IL-22-ActivatedCells · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Frontiers in cellular and infection microbiology · 2021
    Article
  12. Review
  13. JAK3 restrains inflammatory responses and protects against periodontal disease through Wnt3a signaling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  14. JAK-STAT pathway targeting for the treatment of inflammatory bowel disease.Nature reviews. Gastroenterology & hepatology · 2020
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  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

5 authors at 4 institutions in 1 country.

Jayshree MishraFrom the Department of Pharmaceutical Sciences, College of Pharmacy, Texas A&M University System Health Science Center, Kingsville, Texas 78363 and.
Raj K Verma
Gianfranco Alpini
Fanyin Meng
Narendra Kumar
Texas A&M University System · USCentral Texas Veterans Health Care System · USTexas A&M Health Science Center · USTexas A&M University – Kingsville · US

Funding

Role of Cytokine Signaling in Intestinal RestitutionK01DK081661 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI KUMAR, NARENDRA · 2009 to 2013
$631k
NIDDK NIH HHS DK081661NIDDK NIH HHS K01 DK081661
6 · The paper itself

Abstract

Janus kinase 3 (Jak3) is a nonreceptor tyrosine kinase expressed in both hematopoietic and nonhematopoietic cells. Previously, we characterized the functions of Jak3 in cytoskeletal remodeling, epithelial wound healing, and mucosal homeostasis. However, the role of Jak3 in mucosal differentiation and inflammatory bowel disease was not known. In this report, we characterize the role of Jak3 in mucosal differentiation, basal colonic inflammation, and predisposition toward colitis. Using the Jak3 knock-out (KO) mouse model, we show that Jak3 is expressed in colonic mucosa of mice, and the loss of mucosal expression of Jak3 resulted in reduced expression of differentiation markers for the cells of both enterocytic and secretory lineages. Jak3 KO mice showed reduced expression of colonic villin, carbonic anhydrase, secretory mucin muc2, and increased basal colonic inflammation reflected by increased levels of pro-inflammatory cytokines IL-6 and IL-17A in colon along with increased colonic myeloperoxidase activity. The inflammations in KO mice were associated with shortening of colon length, reduced cecum length, decreased crypt heights, and increased severity toward dextran sulfate sodium-induced colitis. In differentiated human colonic epithelial cells, Jak3 redistributed to basolateral surfaces and interacted with adherens junction (AJ) protein β-catenin. Jak3 expression in these cells was essential for AJ localization of β-catenin and maintenance of epithelial barrier functions. Collectively, these results demonstrate the essential role of Jak3 in the colon where it facilitated mucosal differentiation by promoting the expression of differentiation markers and enhanced colonic barrier functions through AJ localization of β-catenin.

Indexed as

Cell DifferentiationGenetic Predisposition to DiseaseAdherens JunctionsAnimalsAntigens, Differentiationbeta CateninCecumCell LineColitisColonEpithelial CellsGene Expression RegulationHumansIntestinal MucosaJanus Kinase 3MiceAntigens, Differentiationbeta CateninJAK3 protein, humanJak3 protein, mouseJanus Kinase 3ColitisDifferentiationInflammatory Bowel DiseaseInnate ImmunityJak Kinaseβ-Catenin

Identifiers

PMID24045942
PMCPMC3814773
OpenAlexW1990814651

What OpenQuestion holds

Textmetadata
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.