Evidence map›Paper›PMID 33159421›Full record

ArticleEMBO reports2020

Class IA PI3Ks regulate subcellular and functional dynamics of IDO1.

Alberta Iacono, Andrea Pompa, Francesca De Marchis, Eleonora Panfili, Francesco A Greco, Alice Coletti, Ciriana Orabona, Claudia Volpi, Maria L Belladonna, Giada Mondanelli and 25 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 43 citations in OpenAlex.

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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

35 authors at 11 institutions in 4 countries.

Alberta IaconoDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Andrea PompaDepartment of Biomolecular Sciences, University Carlo Bo, Urbino, Italy.
Francesca De MarchisInstitute of Biosciences and Bioresources, National Research Council of Italy, Perugia, Italy.
Eleonora PanfiliDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Francesco A GrecoDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy.
Alice ColettiDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy.
Ciriana OrabonaDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Claudia VolpiDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Maria L BelladonnaDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Giada Mondanelli
Elisa AlbiniDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Carmine VaccaDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Marco GargaroDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Francesca FallarinoDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Roberta BianchiDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Carine De Marcos LousaCentre for Biomedical Sciences, School of Clinical and Applied Sciences, Leeds Beckett University, Leeds, UK.
Emilia Mc MazzaIstituto Clinico Humanitas, Rozzano, Italy.
Silvio BicciatoDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0002-1944-7078
Elisa ProiettiDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Francesca MilanoDepartment of Medicine, University of Perugia, Perugia, Italy.
Maria P MartelliDepartment of Medicine, University of Perugia, Perugia, Italy.
Ioana M IamandiiDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Mariona Graupera Garcia-MilaBellvitge Biomedical Research Institute (IDIBELL), Hospitalet de Llobregat, Spain.
Judith Llena SopenaBellvitge Biomedical Research Institute (IDIBELL), Hospitalet de Llobregat, Spain.ORCID 0000-0002-5648-2606
Phillip HawkinsBabraham Institute, Cambridge, UK.
Sabine SuireBabraham Institute, Cambridge, UK.
Klaus OkkenhaugDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID 0000-0002-9432-4051
Anne-Katrien StarkDepartment of Pathology, University of Cambridge, Cambridge, UK.
Fabio GrassiInstitute for Research in Biomedicine, Bellinzona, Switzerland.
Michele BellucciInstitute of Biosciences and Bioresources, National Research Council of Italy, Perugia, Italy.
Paolo PuccettiDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
Laura SantambrogioEnglander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.
Antonio MacchiaruloDepartment of Pharmaceutical Sciences, University of Perugia, Perugia, Italy.ORCID 0000-0001-9535-4183
Ursula GrohmannDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.ORCID 0000-0001-7952-1850
Maria T PallottaDepartment of Experimental Medicine, University of Perugia, Perugia, Italy.
University of Perugia · ITBabraham Institute · GBInstitut d'Investigació Biomédica de Bellvitge · ESInstitute of Biosciences and Bioresources · ITUniversity of Cambridge · GBAlbert Einstein College of Medicine · USCornell University · USFondazione Humanitas per la Ricerca · ITUniversity of Leeds · GBUniversity of Modena and Reggio Emilia · ITUniversity of Urbino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Knowledge of a protein's spatial dynamics at the subcellular level is key to understanding its function(s), interactions, and associated intracellular events. Indoleamine 2,3-dioxygenase 1 (IDO1) is a cytosolic enzyme that controls immune responses via tryptophan metabolism, mainly through its enzymic activity. When phosphorylated, however, IDO1 acts as a signaling molecule in plasmacytoid dendritic cells (pDCs), thus activating genomic effects, ultimately leading to long-lasting immunosuppression. Whether the two activities-namely, the catalytic and signaling functions-are spatially segregated has been unclear. We found that, under conditions favoring signaling rather than catabolic events, IDO1 shifts from the cytosol to early endosomes. The event requires interaction with class IA phosphoinositide 3-kinases (PI3Ks), which become activated, resulting in full expression of the immunoregulatory phenotype in vivo in pDCs as resulting from IDO1-dependent signaling events. Thus, IDO1's spatial dynamics meet the needs for short-acting as well as durable mechanisms of immune suppression, both under acute and chronic inflammatory conditions. These data expand the theoretical basis for an IDO1-centered therapy in inflammation and autoimmunity.

Indexed as

Indoleamine-Pyrrole 2,3,-DioxygenasePhosphatidylinositol 3-KinasesDendritic CellsHumansInflammationSignal TransductionIndoleamine-Pyrrole 2,3,-DioxygenasePhosphatidylinositol 3-Kinasesdendritic cellsearly endosomesindoleamine 2,3-dioxygenase 1 (IDO1)phosphoinositide 3-kinase (PI3K)tryptophan metabolism

Identifiers

PMID33159421
PMCPMC7726814
OpenAlexW3096618019

What OpenQuestion holds

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Registered trials

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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.