Evidence map›Paper›PMID 26967733›Full record

ArticlePloS one2016

The Expression of Bone Morphogenetic Protein 2 and Matrix Metalloproteinase 2 through Retinoic Acid Receptor Beta Induced by All-Trans Retinoic Acid in Cultured ARPE-19 Cells.

Zhenya Gao, Lijun Huo, Dongmei Cui, Xiao Yang, Junwen Zeng

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. All-trans retinoic acid regulates the expression of MMP-2 and TGF-β2International journal of ophthalmology · 2023
    Article
  3. Article
  4. 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

5 authors at 2 institutions in 1 country.

Zhenya GaoState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, SunYat-sen University, No.54 South Xianlie Road, Guangzhou, 510060, P. R. China.
Lijun HuoThe First Affiliated Hospital, Sun Yat-sen University, No.58 Zhong Shan Er Road, Guangzhou 510080, P. R. China.
Dongmei CuiState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, SunYat-sen University, No.54 South Xianlie Road, Guangzhou, 510060, P. R. China.
Xiao YangState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, SunYat-sen University, No.54 South Xianlie Road, Guangzhou, 510060, P. R. China.
Junwen ZengState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, SunYat-sen University, No.54 South Xianlie Road, Guangzhou, 510060, P. R. China.
Sun Yat-sen University · CNZhongshan Ophthalmic Center, Sun Yat-sen University

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAll-trans retinoic acid (ATRA) plays an important role in ocular development. Previous studies found that retinoic acid could influence the metabolism of scleral remodeling by promoting retinal pigment epithelium (RPE) cells to secrete secondary signaling factors. The purpose of this study was to investigate whether retinoic acid affected secretion of bone morphogenetic protein 2 (BMP-2) and matrix metalloproteinase 2 (MMP-2) and to explore the signaling pathway of retinoic acid in cultured acute retinal pigment epithelial 19 (ARPE-19) cells.

methodsThe effects of ATRA (concentrations from 10-9 to 10-5 mol/l) on the expression of retinoic acid receptors (RARs) in ARPE-19 cells were examined at the mRNA and protein levels using reverse transcription-polymerase chain reaction (RT-PCR) and western blot assay, respectively. The effects of treating ARPE-19 cells with ATRA concentrations ranging from 10-9 to 10-5 mol/l for 24 h and 48 h or with 10-6mol/l ATRA at different times ranging from 6h to 72h were assessed using real-time quantitative PCR (qPCR) and enzyme-linked immunosorbent assay (ELISA). The contribution of RARβ-induced activation of ARPE-19 cells was confirmed using LE135, an antagonist of RARβ.

resultsRARβ mRNA levels significantly increased in the ARPE-19 cells treated with ATRA for 24h and 48h. These increases in RARβ mRNA levels were dose dependent (at concentrations of 10-9 to 10-5 mol/l) with a maximum effect observed at 10-6 mol/l. There were no significant changes in the mRNA levels of RARα and RARγ. Western blot assay revealed that RARβ protein levels were increased significantly in a time-dependent manner in ARPE-19 cells treated with 10-6 mol/l ATRA from 12 h to 72 h, with a marked increase observed at 24 h and 48 h. The upregulation of RARβ and the ATRA-induced secretion in ARPE-19 cells could be inhibited by the RARβ antagonist LE135.

conclusionATRA induced upregulation of RARβ in ARPE-19 cells and stimulated these cells to secrete BMP-2 and MMP-2.

Indexed as

Bone Morphogenetic Protein 2Cell LineCell SurvivalDibenzazepinesDose-Response Relationship, DrugGene Expression RegulationHumansMatrix Metalloproteinase 2Receptors, Retinoic AcidRetinal Pigment EpitheliumSignal TransductionTime FactorsTretinoinUp-RegulationBMP2 protein, humanBone Morphogenetic Protein 2DibenzazepinesLE 135Matrix Metalloproteinase 2MMP2 protein, humanReceptors, Retinoic Acidretinoic acid receptor betaTretinoin

Identifiers

PMID26967733
PMCPMC4788292
OpenAlexW2302236701

What OpenQuestion holds

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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.