Evidence map›Paper›PMID 33577398›Full record

ArticleAmerican journal of respiratory cell and molecular biology2021

PINK1 Inhibits Multimeric Aggregation and Signaling of MAVS and MAVS-Dependent Lung Pathology.

Sang-Hun Kim, Hyeon Jun Shin, Chang Min Yoon, Sei Won Lee, Lokesh Sharma, Charles S Dela Cruz, Min-Jong Kang

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
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  4. MicroRNA-27b alleviates septic cardiomyopathy by targeting the Mff/MAVS axis.Frontiers in cellular and infection microbiology · 2025
    Article
  5. Mitochondria in health, disease, and aging.Physiological reviews · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Sang-Hun KimDepartment of Internal Medicine, Section of Pulmonary, Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, Connecticut; and.
Hyeon Jun ShinDepartment of Internal Medicine, Section of Pulmonary, Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, Connecticut; and.
Chang Min YoonDepartment of Internal Medicine, Section of Pulmonary, Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, Connecticut; and.
Sei Won LeeDepartment of Internal Medicine, Section of Pulmonary, Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, Connecticut; and.
Lokesh SharmaDepartment of Internal Medicine, Section of Pulmonary, Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, Connecticut; and.
Charles S Dela CruzDepartment of Internal Medicine, Section of Pulmonary, Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, Connecticut; and.
Min-Jong KangDepartment of Internal Medicine, Section of Pulmonary, Critical Care and Sleep Medicine, Yale University School of Medicine, New Haven, Connecticut; and.
Yale University · USUlsan College · KR

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
The reduction of NLRX1 and its role in pulmonary agingR01AG053495 · NIA · YALE UNIVERSITY · PI KANG, MIN-JONG · 2016 to 2020
$1.7M
Role of NLRX1 in cigarette smoke-induced pulmonary inflammation and remodelingR01HL130283 · NHLBI · YALE UNIVERSITY · PI KANG, MIN-JONG · 2016 to 2019
$1.7M
MAVS-Mediated Pulmonary Inflammation and Injury Response During Cigarette Smoke Exposure and Influenza Viral Infection and in COPDI01BX004661 · VA · VA CONNECTICUT HEALTHCARE SYSTEM · PI DELA CRUZ, CHARLES S · 2020 to 2024
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BLRD VA I01 BX004661NCATS NIH HHS UL1 TR001863NHLBI NIH HHS R01 HL130283NIA NIH HHS R01 AG053495
6 · The paper itself

Abstract

Mitochondria have emerged as important signaling organelles where intracellular perturbations are integrated and, consequently, intracellular signaling pathways are modulated to execute appropriate cellular functions. MAVS (mitochondrial antiviral signaling protein) represents such an example that functions as a platform molecule to mediate mitochondrial innate immune signaling. Recently, multimeric aggregation of MAVS has been identified as a key molecular process for its signaling. The underlying mechanisms to regulate this, however, are still incompletely understood. We hypothesized that PINK1 (PTEN-induced kinase 1) plays an important role in the regulation of multimeric MAVS aggregation and its consequent pathobiology. To test whether PINK1 interacts with MAVS, bimolecular fluorescence complementation analysis and IP were performed. RLH (RIG-I-like helicase) and NLRP3 inflammasome signaling were evaluated by

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBleomycinEpithelial CellsGene Expression RegulationHEK293 CellsHumansImmunity, InnateInflammasomesInfluenza A virusLungMiceMice, KnockoutMitochondriaNLR Family, Pyrin Domain-Containing 3 ProteinOrthomyxoviridae InfectionsAdaptor Proteins, Signal TransducingBleomycinInflammasomesMAVS protein, mouseNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseProtein AggregatesProtein KinasesPTEN-Induced Putative KinaseinflammasomesMAVS aggregationmitochondrial antiviral signaling proteinmitochondrial signalingPTEN‐induced kinase 1

Identifiers

PMID33577398
PMCPMC8086043
OpenAlexW3128989452

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.