Evidence map›Paper›PMID 25299393›Full record

ArticleBiological research2014

Normalization of the levels of inflammatory molecules in Mycobacterium smegmatis-infected U937 cells by fibrate pretreatment.

Sung-Jo Kim, Minho Hong, Ki Duk Song, Hak-Kyo Lee, Sungweon Ryoo, Tae-Hwe Heo

Open access · goldAbstract read
In one paragraph

Article in Biological research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 4 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 4 institutions in 1 country.

Sung-Jo KimDepartment of Biotechnology, Hoseo University, 165, Baebang, Asan, Chungnam, 336-795, Republic of Korea. sungjo@hoseo.edu.
Minho HongDepartment of Biotechnology, Hoseo University, 165, Baebang, Asan, Chungnam, 336-795, Republic of Korea. jlhthanks@naver.com.
Ki Duk SongThe Animal Genomics and Breeding Center, Han-Kyong National University, Anseong, 336-795, Republic of Korea. kiduk.song@gmail.com.
Hak-Kyo LeeThe Animal Genomics and Breeding Center, Han-Kyong National University, Anseong, 336-795, Republic of Korea. breedlee@empas.com.
Sungweon RyooKorean Institute of Tuberculosis, Mansu-ri 482, Gangoe-myeon, Chungcheongbuk-do, 363-954, Cheongwon-gun,Republic of Korea. scientist1@empal.com.
Tae-Hwe HeoLaboratory of Immunology, Integrated Research Institute of Pharmaceutical Sciences, College of Pharmacy, The Catholic University of Korea, Bucheon, 420-743, Republic of Korea. thhur92@catholic.ac.kr.
Hankyong National University · KRHoseo University · KRCatholic University of Korea · KRKorea National Tuberculosis Association · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTuberculosis (TB) is a respiratory tract disease caused by Mycobacterium tuberculosis infection. M. tuberculosis exploits immune privilege to grow and divide in pleural macrophages. Fibrates are associated with the immune response and control lipid metabolism through glycolysis with β-oxidation of fatty acids.

resultsIn this study, we investigated the effect of fibrate pretreatment on the immune response during M. smegmatis infection in U937 cells, a human leukemic monocyte lymphoma cell line. The protein expression of tumor necrosis factor α (TNF-α), an inflammatory marker, and myeloid differentiation primary response gene 88 (MyD88), a toll like receptor adaptor molecule, in the infected group increased at 1 and 6 h after M. smegmatis infection of U937 cells. Acetyl coenzyme A acetyl transferase-1 (ACAT-1), peroxisome proliferator-activated receptor-α (PPAR-α), TNF-α, and MyD88 decreased in U937 cells treated with fibrates at 12 and 24 h after treatment. More than a 24 h pretreatment with fibrate resulted in similar expression levels of ACAT-1 and PPAR-α between infected vehicle control and infected groups which were pretreated with fibrate for 24 h. However, upon exposure to M. smegmatis, the cellular expression of the TNF-α and MyD88 in the infected groups pretreated with fibrate for 24 h decreased significantly compared to that in the infected vehicle group.

conclusionThese results suggest that fibrate pretreatment normalized the levels of inflammatory molecules in Mycobacterium smegmatis-infected U937 cells. Further studies are needed to confirm the findings on pathophysiology and immune defense mechanism of U937 by fibrates during M. tuberculosis infection.

Indexed as

Mycobacterium smegmatisAcetyl-CoA C-AcetyltransferaseBlotting, WesternFibric AcidsHumansInflammation MediatorsMacrophagesMycobacterium InfectionsMyeloid Differentiation Factor 88PPAR alphaSignal TransductionTumor Necrosis Factor-alphaU937 CellsACAT1 protein, humanAcetyl-CoA C-AcetyltransferaseFibric AcidsInflammation MediatorsMyeloid Differentiation Factor 88PPAR alphaTumor Necrosis Factor-alpha

Identifiers

PMID25299393
PMCPMC4177238
OpenAlexW2137579031

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.