Evidence map›Paper›PMID 22500753›Full record

ArticleBiophysical journal2012

Super-resolution imaging of C-type lectin and influenza hemagglutinin nanodomains on plasma membranes using blink microscopy.

Michelle S Itano, Christian Steinhauer, Jürgen J Schmied, Carsten Forthmann, Ping Liu, Aaron K Neumann, Nancy L Thompson, Philip Tinnefeld, Ken Jacobson

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Dectin-1-Mediated DC-SIGN Recruitment toLife (Basel, Switzerland) · 2021
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Optimal structural design of mannosylated nanocarriers for macrophage targeting.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Article
  16. Article
  17. Enhanced receptor-clathrin interactions induced by N-glycan-mediated membrane micropatterning.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

9 authors at 3 institutions in 2 countries.

Michelle S ItanoDepartment of Cell and Developmental Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Christian Steinhauer
Jürgen J Schmied
Carsten Forthmann
Ping Liu
Aaron K Neumann
Nancy L Thompson
Philip Tinnefeld
Ken Jacobson
University of North Carolina at Chapel Hill · USCenter for NanoScience · DETechnische Universität Braunschweig · DE

Funding

STRUCTUREU54GM064346 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI IMPERIALI, BARBARA · 2001 to 2010
$74.9M
Structure and dynamics of membrane microdomains used for viral entry and egressR01GM041402 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JACOBSON, KENNETH A · 1989 to 2016
$4.8M
NIGMS NIH HHS GM-041402NIGMS NIH HHS GM-064346NIGMS NIH HHS R01 GM041402NIGMS NIH HHS U54 GM064346
6 · The paper itself

Abstract

Dendritic cells express DC-SIGN, a C-type lectin (CTL) that binds a variety of pathogens and facilitates their uptake for subsequent antigen presentation. DC-SIGN forms remarkably stable microdomains on the plasma membrane. However, inner leaflet lipid markers are able to diffuse through these microdomains suggesting that, rather than being densely packed with DC-SIGN proteins, an elemental substructure exists. Therefore, a super-resolution imaging technique, Blink Microscopy (Blink), was applied to further investigate the lateral distribution of DC-SIGN. Blink indicates that DC-SIGN, another CTL (CD206), and influenza hemagglutinin (HA) are all localized in small (∼80 nm in diameter) nanodomains. DC-SIGN and CD206 nanodomains are randomly distributed on the plasma membrane, whereas HA nanodomains cluster on length scales up to several microns. We estimate, as a lower limit, that DC-SIGN and HA nanodomains contain on average two tetramers or two trimers, respectively, whereas CD206 is often nonoligomerized. Two-color Blink determined that different CTLs rarely occupy the same nanodomain, although they appear colocalized using wide-field microscopy. What to our knowledge is a novel domain structure emerges in which elemental nanodomains, potentially capable of binding viruses, are organized in a random fashion; evidently, these nanodomains can be clustered into larger microdomains that act as receptor platforms for larger pathogens like yeasts.

Indexed as

NanostructuresAnimalsCell Adhesion MoleculesCell MembraneDC-Specific ICAM-3 Grabbing NonintegrinGlassHemagglutinin Glycoproteins, Influenza VirusHumansLectins, C-TypeMannose-Binding LectinsMannose ReceptorMiceMicroscopyMolecular ImagingNIH 3T3 CellsProtein Structure, TertiaryCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinHemagglutinin Glycoproteins, Influenza VirusLectins, C-TypeMannose-Binding LectinsMannose ReceptorReceptors, Cell Surface

Identifiers

PMID22500753
PMCPMC3318115
OpenAlexW2037037347

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.