Evidence map›Paper›PMID 18843294›Full record

ArticleThe Journal of investigative dermatology2009

Endogenous galectin-3 is localized in membrane lipid rafts and regulates migration of dendritic cells.

Daniel K Hsu, Alexander I Chernyavsky, Huan-Yuan Chen, Lan Yu, Sergei A Grando, Fu-Tong Liu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.2field-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

46 citing papers in PubMed, 103 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Galectins and Liver Diseases.International journal of molecular sciences · 2025
    Review
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  6. Article
  7. Article
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  12. Galectin-3 N-terminal tail prolines modulate cell activity and glycan-mediated oligomerization/phase separation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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  15. Review
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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

6 authors at 3 institutions in 1 country.

Daniel K HsuDepartment of Dermatology, University of California Davis School of Medicine, Sacramento, California 95817, USA. dkhsu@ucdavis.edu
Alexander I Chernyavsky
Huan-Yuan Chen
Lan Yu
Sergei A Grando
Fu-Tong Liu
University of California, Davis · USUniversity of California, Irvine · USUniversity of California System · US

Funding

REGULATION OF TH2 RESPONSES IN ASTHMAP01AI050498 · NIAID · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI ZURAW, BRUCE L. · 2001 to 2005
$5.7M
IGE BINDING PROTEIN--A MULTIFUNCTIONAL ANIMAL LECTINR01AI020958 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI LIU, FU-TONG · 1985 to 2008
$2.0M
Regulation of Keratinocyte Migration by AcetylcholineR01GM062136 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GRANDO, SERGEI A · 2002 to 2010
$1.9M
GALECTINS IN ALLERGIC INFLAMMATIONR01AI039620 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI LIU, FU-TONG · 1997 to 2005
$1.2M
NIAID NIH HHS P01 AI050498NIAID NIH HHS P01 AI50498NIAID NIH HHS R01 AI020958NIAID NIH HHS R01 AI039620NIAID NIH HHS R01 AI20958NIAID NIH HHS R01 AI39620NIGMS NIH HHS GM62136NIGMS NIH HHS R01 GM062136
6 · The paper itself

Abstract

This study reveals a function of endogenous galectin-3, an animal lectin recognizing beta-galactosides, in regulating dendritic cell motility both in vitro and in vivo, which to our knowledge is unreported. First, galectin-3-deficient (gal3(-/-)) bone marrow-derived dendritic cells exhibited defective chemotaxis compared to gal3(+/+) cells. Second, cutaneous dendritic cells in gal3(-/-) mice displayed reduced migration to draining lymph nodes upon hapten stimulation compared to gal3(+/+) mice. Moreover, gal3(-/-) mice were impaired in the development of contact hypersensitivity relative to gal3(+/+) mice in response to a hapten, a process in which dendritic cell trafficking to lymph nodes is critical. In addition, defective signaling was detected in gal3(-/-) cells upon chemokine receptor activation. By immunofluorescence microscopy, we observed that galectin-3 is localized in membrane ruffles and lamellipodia in stimulated dendritic cells and macrophages. Furthermore, galectin-3 was enriched in lipid raft domains under these conditions. Finally, we determined that ruffles on gal3(-/-) cells contained structures with lower complexity compared to gal3(+/+) cells. In view of the participation of membrane ruffles in signal transduction and cell motility, we conclude that galectin-3 regulates cell migration by functioning at these structures.

Indexed as

AnimalsBone Marrow CellsCell LineCell MembraneChemokinesChemotaxisDendritic CellsGalectin 3Lymph NodesMacrophagesMembrane MicrodomainsMiceMicroscopy, FluorescenceModels, BiologicalSignal TransductionChemokinesGalectin 3

Identifiers

PMID18843294
PMCPMC2645233
OpenAlexW2053739815

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.