Evidence map›Paper›PMID 18008083›Full record

ReviewPflugers Archiv : European journal of physiology2008

Receptor trafficking and AFM.

Alexandre Yersin, Pascal Steiner

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pflugers Archiv : European journal of physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Alexandre YersinLaboratory of Biodynamics, Tokyo Institute of Technology, 4259-B8 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan. ayersin@bio.titech.ac.jp
Pascal Steiner

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adaptation of a cell behavior to the environment is possible due to the biochemical and physical information that is transmitted through molecular receptor present at the cell surface. Regulation of receptor distribution and trafficking is thus a key feature to allow cells to properly respond to extracellular signals. Many of the molecular mechanisms that support receptor trafficking occurs at a submicrometric scale and are highly dynamic. Because of its exceptional resolution and its piconewton sensitivity, atomic force microscope (AFM) is a powerful tool to study the trafficking of individual receptors in living cells under near-physiological conditions. In this review, we first describe the general principles of the AFM that allow the detection of single ligand-receptor interaction. We then turn to early studies that demonstrated the ability of AFM to detect individual receptors and map their distribution on the surface of living cell. Finally, we discuss how AFM in combination with optical imaging tools allow the simultaneous investigation of cellular biophysical properties and receptor-trafficking dynamics at the nanometer scale.

Indexed as

Cell Physiological PhenomenaAnimalsBiophysical PhenomenaBiophysicsHumansMicroscopy, Atomic ForceNanotechnologyReceptors, Cell SurfaceReceptors, Cell Surface

Identifiers

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.