Evidence map›Paper›PMID 19855387›Full record

ArticleNature cell biology2009

Intraflagellar transport is required for polarized recycling of the TCR/CD3 complex to the immune synapse.

Francesca Finetti, Silvia Rossi Paccani, Maria Giovanna Riparbelli, Emiliana Giacomello, Giuseppe Perinetti, Gregory J Pazour, Joel L Rosenbaum, Cosima T Baldari

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 197 papers.

0numbers the graph read from it
0cells of the map it votes in
197citing papers in PubMed
12.1field-weighted citation impact, top 1% 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

197 citing papers in PubMed, 299 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Gut microbes · 2026
    Article
  4. Primary cilia dysfunction: A critical driver of metabolic diseases (Review).International journal of molecular medicine · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. The Primary Cilia are Associated with the Axon Initial Segment in Neurons.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  9. Ciliary and Non-Ciliary Roles of IFT88 in Development and Diseases.International journal of molecular sciences · 2025
    Review
  10. Article
  11. Article
  12. Evolutionary trajectory for nuclear functions of ciliary transport complex proteins.Microbiology and molecular biology reviews : MMBR · 2024
    Review
  13. Article
  14. International journal of molecular sciences · 2024
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

137 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 2 countries.

Francesca FinettiDepartment of Evolutionary Biology, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy.
Silvia Rossi Paccani
Maria Giovanna Riparbelli
Emiliana Giacomello
Giuseppe Perinetti
Gregory J Pazour
Joel L Rosenbaum
Cosima T Baldari
University of Siena · ITUniversity of Massachusetts Chan Medical School · USUniversity of Trieste · ITYale University · US

Funding

Intraflagellar Transport Proteins in MiceR01GM060992 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Gregory J Pazour · 2001 to 2026
$10.3M
SYNTHESIS AND ASSEMBLY OF FLAGELLAR PROTEINSR01GM014642 · NIGMS · YALE UNIVERSITY · PI ROSENBAUM, JOEL L · 1985 to 2015
$3.7M
NIGMS NIH HHS GM060992NIGMS NIH HHS R01 GM014642NIGMS NIH HHS R01 GM060992
6 · The paper itself

Abstract

Most eukaryotic cells have a primary cilium which functions as a sensory organelle. Cilia are assembled by intraflagellar transport (IFT), a process mediated by multimeric IFT particles and molecular motors. Here we show that lymphoid and myeloid cells, which lack primary cilia, express IFT proteins. IFT20, an IFT component essential for ciliary assembly, was found to colocalize with both the microtubule organizing centre (MTOC) and Golgi and post-Golgi compartments in T-lymphocytes. In antigen-specific conjugates, IFT20 translocated to the immune synapse. IFT20 knockdown resulted in impaired T-cell receptor/CD3 (TCR/CD3) clustering and signalling at the immune synapse, due to defective polarized recycling. Moreover, IFT20 was required for the inducible assembly of a complex with other IFT components (IFT57 and IFT88) and the TCR. The results identify IFT20 as a new regulator of immune synapse assembly in T cells and provide the first evidence to implicate IFT in membrane trafficking in cells lacking primary cilia, thereby introducing a new perspective on IFT function beyond its role in ciliogenesis.

Indexed as

Biological TransportCarrier ProteinsCD3 ComplexFlagellaGene Knockdown TechniquesHumansImmunological SynapsesReceptors, Antigen, T-CellCarrier ProteinsCD3 ComplexIFT20 protein, humanReceptors, Antigen, T-Cell

Identifiers

PMID19855387
PMCPMC2837911
OpenAlexW2075898272

What OpenQuestion holds

Textmetadata
LicenceTDM
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.