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Original Research Article | OPEN ACCESS

Eriocalyxin B mediates the migration and inflammation of TGF-β2-induced human lens epithelial cells by inhibiting JAK/STAT3 pathway

Xiaomei Feng1, Wenjian Hu2 , Guangjin Wang3, Wei Wang4

1Department of Ophthalmology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan Province, 646000, China; 2Department of Ophthalmology and Otolaryngology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan Province, 646000, China; 3Department of Ophthalmology, Luzhou Longmatan District Aier Eye Hospital Group Company Limited, Luzhou, Sichuan Province, 646000, China; 4Department of Ophthalmology, Kunming Municipal Hospital of Traditional Chinese Medicine, Kunming, Yunnan Province 650000, China.

For correspondence:-  Wenjian Hu   Email: wjhu1851@163.com   Tel:+868303163659

Accepted: 28 February 2023        Published: 31 March 2023

Citation: Feng X, Hu W, Wang G, Wang W. Eriocalyxin B mediates the migration and inflammation of TGF-β2-induced human lens epithelial cells by inhibiting JAK/STAT3 pathway. Trop J Pharm Res 2023; 22(3):493-498 doi: 10.4314/tjpr.v22i3.5

© 2023 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To study the role of Eriocalyxin B (EriB) in the migration and inflammation of TGF-β2-induced human lens epithelial cells (hLECs), and to elucidate the molecular mechanisms involved. 
Methods: The hLECs cultured in vitro were divided into 5 groups, viz, control, TGFβ2, TGFβ2+2 μM EriB, TGFβ2+4 μM EriB, and TGFβ2+8 μM EriB groups. CCK-8, clone formation and Edu labeling assays were performed to assess the effect of EriB on the proliferation of hLECs cells. To determine the role of EriB in cell migration, Transwell and wound healing assays were used. The levels of vimentin, α-SMA, snail, TNF-α,IL-1β,IL-6, P65, p-P65, p-JAK2, JAK2, p-STAT3, STAT3, and β-catenin in hLECs cells were evaluated by enzyme-linked immunosorbent assay (ELISA) and western blot analysis in order ascertain the signaling pathways involved.
Results: The rate of cell proliferation significantly decreased in TGFβ2+2μM EriB, TGFβ2+4μM and TGFβ2+8μM groups compared with TGFβ2 group (p < 0.001). In addition, the migration of hLECs cells and epithelial mesenchymal transition were inhibited by EriB in a dose-dependent way (p < 0.001). ELISA results showed that compared to TGFβ2 group, TNF-α, IL-1β and IL-6 levels in EriB group significantly decreased (p < 0.001). The levels of TNF-α, IL-1β, IL-6, p-P65/P65, p-JAK2/JAK2, p-STAT3/STAT3 and metastasis-associated proteins (α-SMA and snail) in hLECs cells were downregulated by EriB (p < 0.001). Furthermore, vimentin level was increased by EriB (p < 0.001).
Conclusion: The results show that EriB inhibits the growth, metastasis and inflammation of hLECs cells by inhibiting JAK/STAT3 pathway, thus indicating that this pathway is a potential therapeutic target for treating cataract

Keywords: Eriocalyxin B, Posterior capsular opacification, Janus kinase, Signal transducer, Activator of transcription 3, Transforming growth factor beta 2

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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