Evidence map›Paper›PMID 42681017›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Immunofluorescence-Based Study of Cargo Transport Mediated by Cytoskeleton-Associated Molecular Complexes.

Francesca Finetti, Cosima T Baldari

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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.

Francesca FinettiDepartment of Life Sciences, University of Siena, Siena, Italy. francesca.finetti@unisi.it.
Cosima T BaldariDepartment of Life Sciences, University of Siena, Siena, Italy. cosima.baldari@unisi.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cytoskeleton plays a fundamental role in orchestrating the intracellular cargo transport, providing a dynamic scaffold that ensures the appropriate sorting, movement, and distribution of membrane-bound compartments. Through the coordinated activity of microtubules and actin filaments, cargo vesicles are driven along defined routes to ensure efficient intracellular trafficking. Among the molecular machineries that interact with the microtubule network, the intraflagellar transport (IFT) system has emerged as a key regulator of vesicular dynamics. Initially identified for its essential role in ciliogenesis, IFT is now recognized as a broader trafficking coordinator, mediating intracellular transport in different cellular processes. In T lymphocytes, IFT20, in collaboration with other IFT components, orchestrates the selective targeting of recycling vesicles within the endosomal system, promoting the accurate delivery of key receptors and signaling molecules. This chapter provides a detailed immunofluorescence-based protocol to study the role of the IFT system in vesicular trafficking, with a focus on its involvement in receptor recycling to the immune synapse and the retrograde transport of the mannose-6-phosphate receptor to the trans-Golgi network.

Indexed as

CytoskeletonFluorescent Antibody TechniqueAnimalsBiological TransportEndosomesHumansImmunological SynapsesMicrotubulesProtein TransportReceptor, IGF Type 2T-Lymphocytestrans-Golgi NetworkReceptor, IGF Type 2Cargo transportEndosomeIFTImmune synapseImmunofluorescenceMPRRecyclingRetrograde traffickingTCR

Identifiers

What Socratic 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 Socratic graph.