Evidence map›Paper›PMID 33520735›Full record

ArticleFrontiers in cellular and infection microbiology2020

The Mitochondrial Fission Regulator DRP1 Controls Post-Transcriptional Regulation of TNF-α.

Fushan Gao, Mack B Reynolds, Karla D Passalacqua, Jonathan Z Sexton, Basel H Abuaita, Mary X D O'Riordan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed, 30 citations in OpenAlex.

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  20. Maternal Inflammation During Pregnancy and Offspring Brain Development: The Role of Mitochondria.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2022
    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

6 authors at 2 institutions in 2 countries.

Fushan GaoDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, United States.
Mack B ReynoldsDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, United States.
Karla D PassalacquaDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, United States.
Jonathan Z SextonDepartment of Internal Medicine, Gastroenterology, University of Michigan Medical School, Ann Arbor, MI, United States.
Basel H AbuaitaDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, United States.
Mary X D O'RiordanDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, United States.
University of Michigan–Ann Arbor · USCentral South University · CN

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
RESEARCH TRAINING IN EXPERIMENTAL IMMUNOPATHOLOGYT32AI007413 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Bethany B. Moore · 1993 to 2026
$9.8M
Small molecules for expansion of islet beta-cell mass in diabetesR01DK120623 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NEWGARD, CHRISTOPHER B, SEXTON, JONATHAN ZACHARY · 2019 to 2021
$2.0M
Mobilization of lysosome anti-microbial defenses by the unfolded protein responseR21AI101777 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI O'RIORDAN, MARY · 2012 to 2013
$405k
NCI NIH HHS P30 CA046592NIAID NIH HHS R21 AI101777NIAID NIH HHS T32 AI007413NIDDK NIH HHS R01 DK120623
6 · The paper itself

Abstract

The mitochondrial network plays a critical role in the regulation of innate immune signaling and subsequent production of proinflammatory cytokines such as IFN-β and IL-1β. Dynamin-related protein 1 (DRP1) promotes mitochondrial fission and quality control to maintain cellular homeostasis during infection. However, mechanisms by which DRP1 and mitochondrial dynamics control innate immune signaling and the proinflammatory response are incompletely understood. Here we show that macrophage DRP1 is a positive regulator of TNF-α production during sterile inflammation or bacterial infection. Silencing macrophage DRP1 decreased mitochondrial fragmentation and TNF-α production upon stimulation with lipopolysaccharide (LPS) or methicillin-resistant

Indexed as

Methicillin-Resistant Staphylococcus aureusMitochondrial DynamicsDynaminsMitochondriaMitochondrial ProteinsTumor Necrosis Factor-alphaDynaminsMitochondrial ProteinsTumor Necrosis Factor-alphacellular stresscytokineinflammationmacrophagemitochondria

Identifiers

PMID33520735
PMCPMC7840702
OpenAlexW3120755583

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.