Evidence map›Paper›PMID 36834738›Full record

ArticleInternational journal of molecular sciences2023

ATF5 Attenuates the Secretion of Pro-Inflammatory Cytokines in Activated Microglia.

Jiebo Zhu, Min Joung Lee, Jong Hun An, Eungseok Oh, Woosuk Chung, Jun Young Heo

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-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

10 citing papers in PubMed, 20 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

6 authors at 1 institution in 1 country.

Jiebo ZhuDepartment of Medical Science, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea.ORCID 0000-0001-6812-7962
Min Joung LeeDepartment of Medical Science, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea.ORCID 0000-0002-0314-7839
Jong Hun AnDepartment of Medical Science, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea.
Eungseok OhDepartment of Medical Science, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea.
Woosuk ChungDepartment of Medical Science, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea.
Jun Young HeoDepartment of Medical Science, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea.ORCID 0000-0002-0859-0063
Chungnam National University · KR

Funding

Korea Health Industry Development Institute HR20C0025Ministry of Science ICT and Future Planning 2017R1A5A2015385, 2019M3E5D1A02068575, 2020R1A6A3A01097081, 2022R1A2C2002756, 2022R1A2C2006269
6 · The paper itself

Abstract

The highly dynamic changes in microglia necessary to achieve a rapid neuroinflammatory response require a supply of energy from mitochondrial respiration, which leads to the accumulation of unfolded mitochondrial proteins. We previously reported that microglial activation is correlated with the mitochondrial unfolded protein response (UPRmt) in a kaolin-induced hydrocephalus model, but we still do not know the extent to which these changes in microglia are involved in cytokine release. Here, we investigated the activation of BV-2 cells and found that treatment with lipopolysaccharide (LPS) for 48 h increased the secretion of pro-inflammatory cytokines. This increase was accompanied by a concurrent decrease in oxygen consumption rate (OCR) and mitochondrial membrane potential (MMP), in association with the up-regulation of the UPRmt. Inhibition of the UPRmt by knockdown of ATF5, a key upstream regulator of the UPRmt, using small-interfering RNA against ATF5 (siATF5) not only increased production of the pro-inflammatory cytokines, interleukin-6 (IL-6), IL-1β and tumor necrosis factor-α (TNF-α), but also decreased MMP. Our results suggest that ATF5-dependent induction of the UPRmt in microglia acts as a protective mechanism during neuroinflammation and may be a potential therapeutic target for reducing neuroinflammation.

Indexed as

CytokinesMicrogliaActivating Transcription FactorsInflammationLipopolysaccharidesNeuroinflammatory DiseasesTumor Necrosis Factor-alphaActivating Transcription FactorsAtf5 protein, mouseCytokinesLipopolysaccharidesTumor Necrosis Factor-alphaATF5microgliaMMPpro-inflammatory cytokines

Identifiers

PMID36834738
PMCPMC9961550
OpenAlexW4319600303

What OpenQuestion holds

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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.