Evidence map›Paper›PMID 34288802›Full record

ArticleBioengineered2021

G protein-coupled receptor 39 activation alleviates oxidized low-density lipoprotein-induced macrophage inflammatory response, lipid accumulation and apoptosis by inducing A20 expression.

Lu Chen, Zhengdong Fang, Xiaotian Wang, Xiaojie Sun, Xinbao Ge, Can Cheng, Hejie Hu

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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

7 authors at 3 institutions in 1 country.

Lu ChenDepartment of Vascular Surgery, Provincial Hospital Affiliated to Anhui Medical University, Hefei City, Anhui Province, China.
Zhengdong FangDepartment of Vascular Surgery, The First Affiliated Hospital of USTC, Hefei City, Anhui Province, China.
Xiaotian WangDepartment of Vascular Surgery, The First Affiliated Hospital of USTC, Hefei City, Anhui Province, China.
Xiaojie SunDepartment of Vascular Surgery, The First Affiliated Hospital of USTC, Hefei City, Anhui Province, China.
Xinbao GeDepartment of Vascular Surgery, The First Affiliated Hospital of USTC, Hefei City, Anhui Province, China.
Can ChengDepartment of Vascular Surgery, The First Affiliated Hospital of USTC, Hefei City, Anhui Province, China.
Hejie HuDepartment of Vascular Surgery, The First Affiliated Hospital of USTC, Hefei City, Anhui Province, China.
First Affiliated Hospital of Soochow University · CNSoochow University · CNAnhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptor 39 (GPR39) agonist weakens oxidized low-density lipoprotein (ox-LDL)-induced attachment of monocytes to vascular endothelial cells and thus alleviates atherosclerosis. This study looks at whether GPR39 protects macrophages against ox-LDL-induced inflammation and apoptosis and ameliorates lipid accumulation in atherosclerosis and investigates its mechanism. Following inducement of ox-LDL, the expression of GPR39 and tumor necrosis factor alpha-induced protein 3 (TNFAIP3, also known as A20) in Raw 264.7 cells was detected by RT-qPCR and western blotting. The viability of macrophages treated with GPR39 agonist was detected by a cell counting kit 8 kit. GPR39 and A20 expression in ox-LDL-challenged macrophages was assayed by RT-qPCR and western blot with or without GPR30 agonist. After transfection of small interfering RNA (siRNA)-A20, the expression of pro-inflammatory cytokine tumor necrosis factor-α (TNF-α), interleukin (IL)-1β and IL-6 and anti-inflammatory cytokine IL-10 as well as NF-κB p65 and COX2 was detected. Lipid accumulation was observed through Oil Red O Staining. Total cholesterol (TC) and free cholesterol (FC) in macrophages were detected by commercial kits. Lastly, macrophage apoptosis was observed through TUNEL, and apoptosis-related proteins were detected by western blotting . Results indicated that decreased expression of GPR39 and A20 was observed in ox-LDL-induced macrophages. GPR39 agonist significantly increased A20 expression in ox-LDL-treated macrophages. Furthermore, A20 interference reversed the inhibitory effect of GPR39 agonist on ox-LDL-induced inflammation, lipid accumulation, TC and FC overexpression as well as cell apoptosis. In conclusion, activating GPR39 alleviates ox-LDL-induced macrophage inflammation, lipid accumulation and apoptosis in an A20-dependent manner.

Indexed as

ApoptosisAnimalsCytokinesInflammationInflammation MediatorsLipidsLipoproteins, LDLMacrophagesMiceRAW 264.7 CellsReceptors, G-Protein-CoupledTumor Necrosis Factor alpha-Induced Protein 3CytokinesGPR39 protein, mouseInflammation MediatorsLipidsLipoproteins, LDLoxidized low density lipoproteinReceptors, G-Protein-CoupledTnfaip3 protein, mouseTumor Necrosis Factor alpha-Induced Protein 3A20AtherosclerosisGPR39inflammatory responsemacrophage

Identifiers

PMID34288802
PMCPMC8806696
OpenAlexW3184124040

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.