Evidence map›Paper›PMID 37106185›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Dynamics of Immune Cell Microvilli.

En Cai

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. 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, top 93% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

1 author at 1 institution in 1 country.

En CaiDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, USA. encai@andrew.cmu.edu.
Carnegie Mellon University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microvilli are actin-based microscopic membrane protrusions that are present in a wide variety of immune cells. Scanning electron microscopy (SEM) revealed that the T cell surface is covered by microvilli. Growing evidence shows that microvilli play important roles in T cell antigen detection and signal transduction. T cell microvilli are highly dynamic and constantly scan and palpate the opposing antigen-presenting cell (APC) surface in search of antigens. Visualizing the rapid movement of microvilli that are only hundreds of nanometers in size requires imaging technologies with high spatial and temporal resolution. Lattice light-sheet microscopy can achieve diffraction-limited resolution in all three dimensions with a temporal resolution of seconds, making it the perfect tool for studying dynamic events of microvilli during T cell antigen detection and activation. In this chapter, we describe a protocol for imaging localization and movement of T cell microvilli and surface receptors using lattice light-sheet microscopy.

Indexed as

Signal TransductionT-LymphocytesCell MembraneMicroscopy, Electron, ScanningMicrovilli4D live cell imagingLattice light-sheet microscopyMicrovilliT cell activationT cell antigen search

Identifiers

PMID37106185
OpenAlexW4367281452

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.