Evidence map›Paper›PMID 22113485›Full record

ArticleThe Journal of investigative dermatology2012

Real-time visualization of macromolecule uptake by epidermal Langerhans cells in living animals.

Rachel E Frugé, Colleen Krout, Ran Lu, Hironori Matsushima, Akira Takashima

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in The Journal of investigative dermatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Apoptosis and Cell Clearance in Skin Wound Healing.Advances in experimental medicine and biology · 2025
    Review
  3. Article
  4. Intravital multiphoton imaging of cutaneous immune responses.The Journal of investigative dermatology · 2014
    Article
  5. Article
  6. 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 1 institution in 1 country.

Rachel E FrugéDepartment of Medical Microbiology and Immunology, University of Toledo College of Medicine, Toledo, Ohio 43614-5806, USA.
Colleen Krout
Ran Lu
Hironori Matsushima
Akira Takashima
University of Toledo Medical Center · US

Funding

T CELL DEPENDENT TERMINAL MATURATION OF LANGERHANS CELLSR01AR043777 · NIAMS · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI TAKASHIMA, AKIRA · 1996 to 2005
$2.1M
Dendritic Cell-Based Biosensor SystemR01AI055885 · NIAID · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI TAKASHIMA, AKIRA · 2003 to 2005
$1.9M
Behavioral dynamics of Langerhans cells in skinR01AR053355 · NIAMS · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI TAKASHIMA, AKIRA · 2006 to 2010
$1.7M
3D Skin Model to Test Toxic and Sensitizing Potentials of Environmental ChemicalsRC1ES018026 · NIEHS · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI TAKASHIMA, AKIRA · 2009 to 2010
$1000k
LANGERHANS CELL TARGETED GENETIC VACCINE AGAINST HIV1R01AI043262 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI TAKASHIMA, AKIRA · 1998 to 2002
$748k
NIAID NIH HHS R01 AI043262NIAID NIH HHS R01 AI055885NIAMS NIH HHS R01 AR043777NIAMS NIH HHS R01 AR053355NIEHS NIH HHS RC1 ES018026
6 · The paper itself

Abstract

As a skin-resident member of the dendritic cell family, Langerhans cells (LCs) are generally regarded to function as professional antigen-presenting cells. Here we report a simple method to visualize the endocytotic activity of LCs in living animals. BALB/c mice received subcutaneous injection of FITC-conjugated dextran (DX) probes into the ear skin and were then examined under confocal microscopy. Large numbers of FITC(+) epidermal cells became detectable 12-24 hours after injection as background fluorescence signals began to disappear. Most (>90%) of the FITC(+) epidermal cells expressed Langerin, and >95% of Langerin(+) epidermal cells exhibited significant FITC signals. To assess intracellular localization, Alexa Fluor 546-conjugated DX probes were locally injected into IAβ-enhanced green fluorescent protein (EGFP) knock-in mice and Langerin-EGFP-diphtheria toxin receptor mice--three dimensional rotation images showed close association of most of the internalized DX probes with major histocompatibility complex (MHC) class II molecules, but not with Langerin molecules. These observations support the current view that LCs constantly sample surrounding materials, including harmful and innocuous antigens, at the environmental interface. Our data also validate the potential utility of the newly developed imaging approach to monitor LC function in wild-type animals.

Indexed as

EndocytosisAnimalsAntigens, SurfaceDextransFluorescein-5-isothiocyanateFluorescent DyesGreen Fluorescent ProteinsHistocompatibility Antigens Class IILangerhans CellsLectins, C-TypeMannose-Binding LectinsMiceMice, Inbred BALB CMicroscopy, ConfocalQuinolinium CompoundsAlexa fluor 546Antigens, SurfaceCd207 protein, mouseDextransenhanced green fluorescent proteinFluorescein-5-isothiocyanatefluorescein isothiocyanate dextranFluorescent DyesGreen Fluorescent ProteinsHistocompatibility Antigens Class IILectins, C-TypeMannose-Binding LectinsQuinolinium Compounds

Identifiers

PMID22113485
PMCPMC3278540
OpenAlexW2069795195

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.