Evidence map›Paper›PMID 20007837›Full record

ArticleInvestigative ophthalmology & visual science2010

Epifluorescence intravital microscopy of murine corneal dendritic cells.

Ellen J Lee, James T Rosenbaum, Stephen R Planck

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

35 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
  4. Article
  5. Article
  6. Article
  7. Diurnal changes and topographical distribution of ocular surface epithelial dendritic cells in humans, and repeatability of density and morphology assessment.Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) · 2023
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Corneal Immune Cells Are Increased in Patients With Multiple Sclerosis.Translational vision science & technology · 2021
    Article
  13. Article
  14. Article
  15. In vivo immune cell dynamics in the human cornea.Experimental eye research · 2020
    Observational
  16. Article
  17. Kinetics of corneal leukocytes by intravital multiphoton microscopy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  18. Article
  19. 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.

Ellen J LeeDepartments of Ophthalmology, Cell and Developmental Biology, Oregon Health and Science University, Portland, Oregon, USA. leee@ohsu.edu
James T Rosenbaum
Stephen R Planck
Ophthalmology Associates (United States) · US

Funding

FOUR DIMENTIONAL IMAGING OF THE IMMUNE RESPONSE IN VIVOR01EY013093 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI ROSENBAUM, JAMES T · 1999 to 2010
$5.0M
In vivo imaging of corneal inflammationK08EY015448 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEE, ELLEN J · 2004 to 2008
$554k
NEI NIH HHS EY015448NEI NIH HHS EY13093NEI NIH HHS K08 EY015448NEI NIH HHS R01 EY013093
6 · The paper itself

Abstract

Purpose. Dendritic cells (DCs) are antigen-presenting cells vital for initiating immune responses. In this study the authors examined the in vivo migratory capability of resident corneal DCs to various stimuli. Methods. The authors used mice expressing enhanced yellow fluorescent protein (eYFP) under control of the CD11c promoter to visualize corneal DCs. To assess the distribution and mobility of DCs, normal corneas were imaged in vivo and ex vivo with fluorescence microscopy. Intravital microscopy was used to examine the responses of resident central and peripheral corneal DCs to silver nitrate injury, lipopolysaccharide, microspheres, and tumor necrosis factor (TNF-alpha). In some experiments, TNF-alpha injection was used to first induce centripetal migration of DCs to the central cornea, which was subsequently reinjected with microspheres. Results. In normal corneas, DCs were sparsely distributed centrally and were denser in the periphery, with epithelial-level DCs extending into the epithelium. Videomicroscopy showed that though cell processes were in continuous movement, cells generally did not migrate. Within the first 6 hours after stimulation, neither central nor peripheral corneal DCs exhibited significant lateral migration, but central corneal DCs assumed extreme morphologic changes. An increased number of DCs in the TNF-alpha-stimulated central cornea were responsive to subsequent microsphere injection by adopting a migratory behavior, but not with increased speed. Conclusions. In vivo imaging reveals minimal lateral migration of corneal DCs after various stimuli. In contrast, DCs within the central cornea after initial TNF-alpha injection are more likely to respond to a secondary insult with lateral migration.

Indexed as

AnimalsCell MovementCorneaDendritic CellsFluorescent DyesLipopolysaccharidesLuminescent ProteinsMiceMice, Inbred C57BLMicroscopy, FluorescenceSilver NitrateTumor Necrosis Factor-alphaFluorescent DyesLipopolysaccharidesLuminescent ProteinsSilver NitrateTumor Necrosis Factor-alpha

Identifiers

PMID20007837
PMCPMC2868401
OpenAlexW2073565924

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.