Experimental Eye Research, Год журнала: 2024, Номер 251, С. 110213 - 110213
Опубликована: Дек. 18, 2024
Язык: Английский
Experimental Eye Research, Год журнала: 2024, Номер 251, С. 110213 - 110213
Опубликована: Дек. 18, 2024
Язык: Английский
Journal of Ocular Pharmacology and Therapeutics, Год журнала: 2025, Номер unknown
Опубликована: Фев. 17, 2025
Purpose: Ocular trauma leads to loss of corneal clarity resulting in vision deficits. Autophagy plays a critical role the extracellular matrix, tissue repair, and homeostasis but its precise mechanistic regulating function remains unknown. The present study investigated modulation autophagy-related genes (LC3, Beclin1, Sqstm1/p62, Lamp1) healthy injured canine stromal fibroblasts (CSFs).
Язык: Английский
Процитировано
0Experimental Eye Research, Год журнала: 2023, Номер 235, С. 109644 - 109644
Опубликована: Сен. 7, 2023
Язык: Английский
Процитировано
9Experimental Eye Research, Год журнала: 2024, Номер 248, С. 110073 - 110073
Опубликована: Сен. 6, 2024
Язык: Английский
Процитировано
2Cells, Год журнала: 2024, Номер 13(23), С. 2021 - 2021
Опубликована: Дек. 6, 2024
Mustard gas keratopathy (MGK), a complication of exposure to sulfur mustard, is blinding ocular surface disease involving key cellular pathways, including apoptosis, oxidative stress, and inflammation. Recent studies indicate that senescence contributes the pathophysiology mustard toxicity. This study aimed assess stress-related pathways-particularly mitogen-activated protein kinase (MAPK) signaling-in nitrogen (NM)-induced corneal injury. In vitro, primary human epithelial (P-HCECs), mesenchymal stromal cells (hcMSCs), corneal-limbal cell (HCLE) lines were exposed varying concentrations NM. The results demonstrated dose-dependent increase in senescence, characterized by reduced Ki67 expression, elevated p16, p21 mRNA levels, as well activation MAPK pathway activation. Treatment with selective p38-MAPK inhibitor significantly markers improved proliferation following Overall, these NM triggers signaling, while inhibition mitigates effects, suggesting potential therapeutic strategy.
Язык: Английский
Процитировано
1Toxicology Letters, Год журнала: 2024, Номер 396, С. 70 - 80
Опубликована: Апрель 25, 2024
Язык: Английский
Процитировано
0International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(12), С. 6560 - 6560
Опубликована: Июнь 14, 2024
Human corneal fibrosis can lead to opacity and ultimately partial or complete vision loss. Currently, transplantation is the only treatment for severe comes with risk of rejection donor shortages. Sphingolipids (SPLs) are known modulate in various tissues organs, including cornea. We previously reported that SPLs tightly related both, transforming growth factor beta (TGF-β) signaling fibrogenesis. The aim this study was investigate effects sphingosine-1-phosphate (S1P) S1P inhibition on specific TGF-β SPL family members fibrosis. Healthy human fibroblasts (HCFs) were isolated cultured EMEM + FBS VitC (construct medium) 3D transwells 4 weeks. following treatments prepared a construct medium: 0.1 ng/mL TGF-β1 (β1), 1 μM (S1P), 5 Sphingosine kinase inhibitor 2 (I2). Five groups tested: (1) control (no treatment); rescue groups; (2) β1/S1P; (3) β1/I2; prevention (4) S1P/β1; (5) I2/β1. Each administered weeks one switched another Using Western blot analysis, constructs examined expression fibrotic markers, SPL, pathway members. Scratch assays from 2D cultures also utilized evaluate cell migration observed reduced inactivation latent binding proteins (LTBPs), receptors, Suppressor Mothers Against Decapentaplegic homologs (SMADs), I2 compared rescue, respectively. Furthermore, we increased stimulation groups, decreased after 12 h 18 post-scratch. have demonstrated modulated LTBPs, SPLs, canonical downstream SMAD pathway. Further investigations warranted order fully uncover potential utilizing SphK as novel therapy
Язык: Английский
Процитировано
0Cell Biochemistry and Biophysics, Год журнала: 2024, Номер unknown
Опубликована: Дек. 15, 2024
Язык: Английский
Процитировано
0Experimental Eye Research, Год журнала: 2024, Номер 251, С. 110213 - 110213
Опубликована: Дек. 18, 2024
Язык: Английский
Процитировано
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