Evidence map›Paper›PMID 27905556›Full record

ArticleScientific reports2016

Cellular aspartyl proteases promote the unconventional secretion of biologically active HIV-1 matrix protein p17.

Francesca Caccuri, Maria Luisa Iaria, Federica Campilongo, Kristen Varney, Alessandro Rossi, Stefania Mitola, Silvia Schiarea, Antonella Bugatti, Pietro Mazzuca, Cinzia Giagulli and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Secreted Nonstructural Protein 3 is a Pathogenic Determinant of Orbivirus.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  8. HIV-1 mutants expressing B cell clonogenic matrix protein p17 variants are increasing their prevalence worldwide.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  11. Evolution toward beta common chain receptor usage links the matrix proteins of HIV-1 and its ancestors to human erythropoietin.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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

14 authors at 4 institutions in 2 countries.

Francesca CaccuriDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
Maria Luisa IariaDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
Federica CampilongoDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
Kristen VarneyDepartment of Biochemistry and Molecular Biology, University of Maryland, Baltimore, Maryland, USA.
Alessandro RossiIRCCS Istituto di Ricerche Farmacologiche "Mario Negri" Milan, Italy.
Stefania MitolaDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
Silvia SchiareaIRCCS Istituto di Ricerche Farmacologiche "Mario Negri" Milan, Italy.
Antonella BugattiDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
Pietro MazzucaDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
Cinzia GiagulliDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
Simona FiorentiniDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
Wuyuan LuInstitute of Human Virology, University of Maryland, Baltimore, Maryland, USA.
Mario SalmonaIRCCS Istituto di Ricerche Farmacologiche "Mario Negri" Milan, Italy.
Arnaldo CarusoDepartment of Molecular and Translational Medicine, University of Brescia Medical School, Brescia, Italy.
University of Brescia · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Maryland, Baltimore · USMario Negri Institute for Pharmacological Research · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human immune deficiency virus type 1 (HIV-1) matrix protein p17 (p17), although devoid of a signal sequence, is released by infected cells and detected in blood and in different organs and tissues even in HIV-1-infected patients undergoing successful combined antiretroviral therapy (cART). Extracellularly, p17 deregulates the function of different cells involved in AIDS pathogenesis. The mechanism of p17 secretion, particularly during HIV-1 latency, still remains to be elucidated. A recent study showed that HIV-1-infected cells can produce Gag without spreading infection in a model of viral latency. Here we show that in Gag-expressing cells, secretion of biologically active p17 takes place at the plasma membrane and occurs following its interaction with phosphatidylinositol-(4,5)-bisphosphate and its subsequent cleavage from the precursor Gag (Pr55

Indexed as

Aspartic Acid ProteasesCell Membranegag Gene Products, Human Immunodeficiency VirusHeLa CellsHIV-1HIV AntigensHIV InfectionsHumansJurkat CellsPhosphatidylinositol 4,5-DiphosphateProtein PrecursorsVirus LatencyAspartic Acid Proteasesgag Gene Products, Human Immunodeficiency VirusHIV Antigensp17 protein, Human Immunodeficiency Virus Type 1p55 gag precursor protein, Human immunodeficiency virus 1Phosphatidylinositol 4,5-DiphosphateProtein Precursors

Identifiers

PMID27905556
PMCPMC5131311
OpenAlexW2558271420

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.