Evidence map›Paper›PMID 31142807›Full record

ArticleCell death and differentiation2020

The intraflagellar transport protein IFT20 controls lysosome biogenesis by regulating the post-Golgi transport of acid hydrolases.

Francesca Finetti, Chiara Cassioli, Valentina Cianfanelli, Anna Onnis, Eugenio Paccagnini, Anna Kabanova, Cosima T Baldari

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Guideline
  2. Primary cilia dysfunction: A critical driver of metabolic diseases (Review).International journal of molecular medicine · 2026
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  13. Autophagy: A Double-Edged Sword in Male Reproduction.International journal of molecular sciences · 2022
    Review
  14. Review
  15. Review
  16. Review
  17. 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

7 authors at 2 institutions in 2 countries.

Francesca FinettiDepartment of Life Sciences, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy. finetti4@unisi.it.ORCID http://orcid.org/0000-0002-3421-1637
Chiara CassioliDepartment of Life Sciences, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy.ORCID http://orcid.org/0000-0002-4853-2298
Valentina CianfanelliCell Stress and Survival Unit, Danish Cancer Society Research Center, 2100, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-3857-9463
Anna OnnisDepartment of Life Sciences, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy.ORCID http://orcid.org/0000-0003-3199-9868
Eugenio PaccagniniDepartment of Life Sciences, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy.
Anna KabanovaDepartment of Life Sciences, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy.
Cosima T BaldariDepartment of Life Sciences, University of Siena, Via Aldo Moro 2, 53100, Siena, Italy. cosima.baldari@unisi.it.
University of Siena · ITDanish Cancer Society · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The assembly and function of the primary cilium depends on multimolecular intraflagellar transport (IFT) complexes that shuttle their cargo along the axonemal microtubules through their interaction with molecular motors. The IFT system has been moreover recently implicated in a reciprocal interplay between autophagy and ciliogenesis. We have previously reported that IFT20 and other components of the IFT complexes participate in the assembly of the immune synapse in the non-ciliated T cell, suggesting that other cellular processes regulated by the IFT system in ciliated cells, including autophagy, may be shared by cells lacking a cilium. Starting from the observation of a defect in autophagic clearance and an accumulation of lipid droplets in IFT20-deficient T cells, we show that IFT20 is required for lysosome biogenesis and function by controlling the lysosomal targeting of acid hydrolases. This function involves its ability to regulate the retrograde traffic of the cation-independent mannose-6-phosphate receptor (CI-MPR) to the trans-Golgi network, which is achieved by coupling recycling CI-MPRs to the microtubule motor dynein. Consistent with the lysosomal defect, an upregulation of the TFEB-dependent expression of the lysosomal gene network can be observed in IFT20-deficient cells, which is associated with defective tonic T-cell antigen receptor signaling and mTOR activity. We additionally show that the lysosome-related function of IFT20 extends to non-ciliated cells other than T cells, as well as to ciliated cells. Our findings provide the first evidence that a component of the IFT system that controls ciliogenesis is implicated in the biogenesis of lysosomes.

Indexed as

AutophagyBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCarrier ProteinsCell LineCiliaDyneinsHumansJurkat CellsLysosomesOrganelle BiogenesisPeptide HydrolasesProtein TransportReceptor, IGF Type 2T-Lymphocytestrans-Golgi NetworkBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCarrier ProteinsDyneinsIFT20 protein, humanPeptide HydrolasesReceptor, IGF Type 2TFEB protein, human

Identifiers

PMID31142807
PMCPMC7205998
OpenAlexW2947253536

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.