Evidence map›Paper›PMID 19233848›Full record

ArticleThe Journal of biological chemistry2009

CCR6 regulation of the actin cytoskeleton orchestrates human beta defensin-2- and CCL20-mediated restitution of colonic epithelial cells.

Rebecca A Vongsa, Noah P Zimmerman, Michael B Dwinell

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
  2. Colonic epithelial regeneration shapes susceptibility tobioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Anti-integrin αvβ6 Autoantibodies Are Increased in Primary Sclerosing Cholangitis Patients With Concomitant Inflammatory Bowel Disease and Correlate With Liver Disease Severity.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2025
    Article
  5. Article
  6. Article
  7. Mechanisms and regulation of defensins in host defense.Signal transduction and targeted therapy · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Glucocorticoids promote CCL20 expression in keratinocytes.The British journal of dermatology · 2021
    Article
  16. International journal of medical sciences · 2021
    Article
  17. Article
  18. Review
  19. Expression and Function of Host Defense Peptides at Inflammation Sites.International journal of molecular sciences · 2019
    Review
  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

3 authors at 1 institution in 1 country.

Rebecca A VongsaDepartment of Microbiology and Molecular Genetics, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.
Noah P Zimmerman
Michael B Dwinell
Medical College of Wisconsin · US

Funding

EPITHELIAL CXCR4 IN A MUCOSAL COMMUNICATION NETWORKR01DK062066 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI DWINELL, MICHAEL B · 2005 to 2009
$1.4M
Epithelial CXCR4 in a Mucosal Communication NetworkR56DK062066 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI DWINELL, MICHAEL B · 2010 to 2010
$329k
NIDDK NIH HHS DK062066NIDDK NIH HHS R01 DK062066
6 · The paper itself

Abstract

Intestinal inflammation is exacerbated by defects in the epithelial barrier and subsequent infiltration of microbes and toxins into the underlying mucosa. Production of chemokines and antimicrobial peptides by an intact epithelium provide the first line of defense against invading organisms. In addition to its antimicrobial actions, human beta defensin-2 (HBD2) may also stimulate the migration of dendritic cells through binding the chemokine receptor CCR6. As human colonic epithelium expresses CCR6, we investigated the potential of HBD2 to stimulate intestinal epithelial migration. Using polarized human intestinal Caco2 and T84 cells and non-transformed IEC6 cells, HBD2 was equipotent to CCL20 in stimulating migration. Neutralizing antibodies confirmed HBD2 and CCL20 engagement to CCR6 were sufficient to induce epithelial cell migration. Consistent with restitution, motogenic concentrations of HBD2 and CCL20 did not induce proliferation. Stimulation with those CCR6 ligands leads to calcium mobilization and elevated active RhoA, phosphorylated myosin light chain, and F-actin accumulation. HBD2 and CCL20 were unable to stimulate migration in the presence of either Rho-kinase or phosphoinositide 3-kinase inhibitors or an intracellular calcium chelator. Together, these data indicate that the canonical wound healing regulatory pathway, along with calcium mobilization, regulates CCR6-directed epithelial cell migration. These findings expand the mechanistic role for chemokines and HBD2 in mucosal inflammation to include immunocyte trafficking and killing of microbes with the concomitant activation of restitutive migration and barrier repair.

Indexed as

Gene Expression Regulation, NeoplasticActinsAnimalsbeta-DefensinsCaco-2 CellsCell Line, TumorCell MovementCell ProliferationChemokine CCL20ChemokinesCytoskeletonHumansMyosin Light ChainsRatsReceptors, CCR6Actinsbeta-DefensinsCCL20 protein, humanCCR6 protein, humanChemokine CCL20ChemokinesDEFB4A protein, humanMyosin Light ChainsReceptors, CCR6

Identifiers

PMID19233848
PMCPMC2665058
OpenAlexW1997929840

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.