Evidence map›Paper›PMID 35716284›Full record

ArticleMolecular biology reports2022

D-aspartic acid protects against gingival fibroblasts inflammation by suppressing pyroptosis.

Xuechun Du, Baosheng Li, Qing Cai, Shuwei Qiao, Zixuan Wang, Zhen Li, Yuyang Li, Weiyan Meng

Abstract read
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In one paragraph

Article in Molecular biology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

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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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

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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

8 authors at 1 institution in 1 country.

Xuechun Du *Department of Dental Implantology, Hospital of Stomatology, Jilin University, 130021, Changchun, Jilin, China.
Baosheng Li *Department of Dental Implantology, Hospital of Stomatology, Jilin University, 130021, Changchun, Jilin, China.
Qing CaiDepartment of Dental Implantology, Hospital of Stomatology, Jilin University, 130021, Changchun, Jilin, China.
Shuwei QiaoDepartment of Dental Implantology, Hospital of Stomatology, Jilin University, 130021, Changchun, Jilin, China.
Zixuan WangDepartment of Dental Implantology, Hospital of Stomatology, Jilin University, 130021, Changchun, Jilin, China.
Zhen LiDepartment of Dental Implantology, Hospital of Stomatology, Jilin University, 130021, Changchun, Jilin, China.
Yuyang LiDepartment of Dental Implantology, Hospital of Stomatology, Jilin University, 130021, Changchun, Jilin, China.
Weiyan MengDepartment of Dental Implantology, Hospital of Stomatology, Jilin University, 130021, Changchun, Jilin, China. mengwy@jlu.edu.cn.ORCID http://orcid.org/0000-0001-6870-4774
Jilin University · CN

Funding

Department of Finance of Jilin Province JCSZ2019378-3Department of Science and Technology of Jilin Province 20200404108YY
6 · The paper itself

Abstract

backgroundPeri-implantitis is the main cause of dental implant failure, which is associated with pyroptosis. The roles of D-aspartic acid (D-Asp) on pyroptosis and the mechanism of the protective effect of D-Asp on human gingival fibroblasts (HGFs) remain unknown. This study investigated the effects of D-Asp on the pyroptosis of HGFs induced by high mobility group box 1 protein (HMGB1).

methodsThe cytotoxic effects of D-Asp on HGFs was detected by Cell Counting Kit-8 assay, the membrane permeability was investigated by propidium iodide/ Hoechst 33,342 double staining, flow cytometry analysis, and lactate dehydrogenase releasing, The gene and protein expression levels were detected by real-time quantitative PCR, enzyme-linked immunosorbent assay, and Western blot, respectively.

resultsCell viability analysis showed that D-Asp ≤ 30 mM had no cytotoxicity to HGFs. HMGB1 drastically raised the membrane permeability of HGFs, while 1/10/30 mM D-Asp suppressed the permeability and remained the integrity of the membrane. HMGB1 promoted the mRNA expression of NLRP3, caspase-1, GSDMD, IL-1β, and IL-18, and the protein expression of IL-1β, IL-18, caspase-1, GSDMD, and NLRP3.

conclusionsWith the pretreatment of HGFs with D-Asp of 1/10/30 mM for 24 h, the cell membrane permeability was reduced and the expression of NLRP3, caspase-1, GSDMD, IL-1β, and IL-18 was significantly decreased compared with the HMGB1 group, indicating the competitive antagonism of D-Asp against HMGB1 on the binding with toll-like receptors. Hence, this study may provide a novel insight into preventing pyroptosis and propose a new strategy for the treatment of peri-implantitis.

Indexed as

HMGB1 ProteinPeri-ImplantitisCaspase 1D-Aspartic AcidFibroblastsHumansInflammationInterleukin-18Interleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinPyroptosisCaspase 1D-Aspartic AcidHMGB1 ProteinInterleukin-18Interleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinD-aspartic acidFibroblastHMGB1Peri-implantitisPyroptosis

Identifiers

PMID35716284
OpenAlexW4283067347

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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.