Evidence map›Paper›PMID 39109744›Full record

ArticleArquivos brasileiros de oftalmologia2024

Hyaluronic acid-mediated epithelial-mesenchymal transition of human lens epithelial cells via CD44 and TGF-β2.

Yumin Gui, Jianjun Peng, Shuanghong Jiang

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Article in Arquivos brasileiros de oftalmologia, 2024. 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
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yumin GuiWuhan Puren Hospital, Qingshan District Jianshe Fourth Road Benxi Street Te #1, Wuhan, Hubei Province, China.ORCID 0009-0004-5395-442X
Jianjun PengWuhan Puren Hospital, Qingshan District Jianshe Fourth Road Benxi Street Te #1, Wuhan, Hubei Province, China.ORCID 0009-0007-6461-3091
Shuanghong JiangWuhan University Renmin Hospital, Wuchang District Ziyang Road 22, Wuhan, Hubei Province, China.ORCID 0009-0000-1040-3215

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe epithelial-mesenchymal transition of human lens epithelial cells plays a role in posterior capsule opacification, a fibrotic process that leads to a common type of cataract. Hyaluronic acid has been implicated in this fibrosis. Studies have investigated the role of transforming growth factor (TGF)-β2 in epithelial-mesenchymal transition. However, the role of TGF-β2 in hyaluronic acid-mediated fibrosis of lens epithelial cell remains unknown. We here examined the role of TGF-β2 in the hyaluronic acid-mediated epithelial-mesenchymal transition of lens epithelial cells.

methodsCultured human lens epithelial cells (HLEB3) were infected with CD44-siRNA by using the Lipofectamine 3000 transfection reagent. The CCK-8 kit was used to measure cell viability, and the scratch assay was used to determine cell migration. Cell oxidative stress was analyzed in a dichloro-dihydro-fluorescein diacetate assay and by using a flow cytometer. The TGF-β2 level in HLEB3 cells was examined through immunohistochemical staining. The TGF-β2 protein level was determined through western blotting. mRNA expression levels were determined through quantitative real-time polymerase chain reaction.

resultsTreatment with hyaluronic acid (1.0 μM, 24 h) increased the epithelial-mesenchymal transition of HLEB3 cells. The increase in TGF-β2 levels corresponded to an increase in CD44 levels in the culture medium. However, blocking the CD44 function significantly reduced the TGF-β2-mediated epithelial-mesenchymal transition response of HLEB3 cells.

conclusionsOur study showed that both CD44 and TGF-β2 are critical contributors to the hyaluronic acid-mediated epithelial-mesenchymal transition of lens epithelial cells, and that TGF-β2 in epithelial-mesenchymal transition is regulated by CD44. These results suggest that CD44 could be used as a target for preventing hyaluronic acid-induced posterior capsule opacification. Our findings suggest that CD44/TGF-β2 is crucial for the hyaluronic acid-induced epithelial-mesenchymal transition of lens epithelial cells.

Indexed as

Cell MovementEpithelial CellsEpithelial-Mesenchymal TransitionHyaluronan ReceptorsHyaluronic AcidLens, CrystallineTransforming Growth Factor beta2Blotting, WesternCapsule OpacificationCells, CulturedCell SurvivalFlow CytometryHumansImmunohistochemistryOxidative StressReal-Time Polymerase Chain ReactionCD44 protein, humanHyaluronan ReceptorsHyaluronic AcidTransforming Growth Factor beta2

Identifiers

PMID39109744
PMCPMC12585068

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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.