Evidence map›Paper›PMID 32425938›Full record

ReviewFrontiers in immunology2020

Involvement of the TRPML Mucolipin Channels in Viral Infections and Anti-viral Innate Immune Responses.

Giorgio Santoni, Maria Beatrice Morelli, Consuelo Amantini, Massimo Nabissi, Matteo Santoni, Angela Santoni

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Transient receptor potential channels inChannels (Austin, Tex.) · 2026
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  13. Unveiling the impact of lysosomal ion channels: balancing ion signaling and disease pathogenesis.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2023
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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

6 authors at 3 institutions in 1 country.

Giorgio SantoniImmunopathology Laboratory, School of Pharmacy, University of Camerino, Camerino, Italy.
Maria Beatrice MorelliImmunopathology Laboratory, School of Pharmacy, University of Camerino, Camerino, Italy.
Consuelo AmantiniImmunopathology Laboratory, School of Biosciences and Veterinary Medicine, University of Camerino, Camerino, Italy.
Massimo NabissiImmunopathology Laboratory, School of Pharmacy, University of Camerino, Camerino, Italy.
Matteo SantoniMedical Oncology Unit, Hospital of Macerata, Macerata, Italy.
Angela SantoniDepartment of Molecular Medicine, Sapienza University, Rome, Italy.
Università di Camerino · ITSapienza University of Rome · ITUniversity of Macerata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TRPML channels (TRPML1, TRPML2, and TRPML3), belonging to the mucolipin TRP subfamily, primary localize to a population of membrane-bonded vesicles along the endocytosis, and exocytosis pathways. Human viruses enter host cells by plasma membrane penetration or by receptor-mediated endocytosis. TRPML2 enhances the infectivity of a number of enveloped viruses by promoting virus vesicular trafficking and escape from endosomal compartment. TRPML2 expression is stimulated by interferon and by several toll like receptor (TLR) activators, suggesting a possible role in the activation of the innate immune response. Noteworthy, TRPML1 plays a major role in single strand RNA/DNA trafficking into lysosomes and the lack of TRPML1 impairs the TLR-7 and TLR-9 ligand transportation to lysosomes resulting in decreased dendritic cell maturation/activation and migration to the lymph nodes. TRPML channels are also expressed by natural killer (NK) cells, a subset of innate lymphocytes with an essential role during viral infections; recent findings have indicated a role of TRPML1-mediated modulation of secretory lysosomes in NK cells education. Moreover, as also NK cells express TLR recognizing viral pattern, an increased TLR-mediated activation of cytokine production can be envisaged, suggesting a dual role in the NK cell-mediated antiviral responses. Overall, TRPML channels might play a double-edged sword in resistance to viral infections: on one side they can promote virus cellular entry and infectivity; on the other side, by regulating TLR responses in the various immune cells, they contribute to enhance antiviral innate and possibly adaptive immune responses.

Indexed as

AnimalsBiological TransportCell MembraneEndocytosisEndosomesHumansImmunity, InnateKiller Cells, NaturalLysosomesMiceToll-Like ReceptorsTransient Receptor Potential ChannelsVirus DiseasesMCOLN1 protein, humanMcoln2 protein, humanMCOLN3 protein, humanToll-Like ReceptorsTransient Receptor Potential Channelsendolysosomeinnate immunitymucolipinTRP channelviral infection

Identifiers

PMID32425938
PMCPMC7212413
OpenAlexW3022991462

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.