Covariation of scleral remodeling and PI3K/Akt signaling pathway in experimental myopia

被引:0
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作者
Xiaomeng Li [1 ]
Xiaojing Liu [2 ]
Yingxin Yu [1 ]
Tuling Li [1 ]
Lijie Guo [1 ]
Guili Hu [3 ]
Huixia Wei [1 ]
Zhaohui Yang [4 ]
Jinpeng Liu [1 ]
Yixian Hao [1 ]
Ruixue Zhang [4 ]
Qiuxin Wu [1 ]
Xuan Liao [4 ]
Dadong Guo [5 ]
Hongsheng Bi [6 ]
机构
[1] Shandong University of Traditional Chinese Medicine,School of Ophthalmology and Optometry
[2] Wenzhou Medical University,Guangzhou laboratory
[3] Guangzhou Medical University,Department of Ophthalmology of Affiliated Hospital and Medical School of Ophthalmology and Optometry
[4] Affiliated Eye Hospital of Shandong University of Traditional Chinese Medicine,Medical College of Optometry and Ophthalmology
[5] North Sichuan Medical College,Medical College of Optometry and Ophthalmology
[6] Shandong Provincial Key Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Therapy of Ocular Diseases,undefined
[7] Shandong Academy of Eye Disease Prevention and Therapy,undefined
[8] Shandong University of Traditional Chinese Medicine,undefined
[9] Shandong Academy of Eye Disease Prevention and Therapy,undefined
[10] Shandong University of Traditional Chinese Medicine,undefined
关键词
Experimental myopia; PI3K/Akt signaling pathway; TGF-β1; Collagen; Scleral remodeling;
D O I
10.1038/s41598-025-97643-7
中图分类号
学科分类号
摘要
The present study aimed to investigate the role of the PI3K/Akt signaling pathway in scleral remodeling in the development of negative lens-induced myopia (LIM). The change of scleral morphology in experimental myopic guinea pigs was observed by transmission electron microscopy, Masson staining, and TUNEL assay, respectively. Meanwhile, the levels of the PI3K/AKT signaling pathway- and scleral remodeling-related molecules in scleral tissues were determined by real-time quantitative PCR (qPCR), enzyme-linked immunosorbent assay (ELISA), immunofluorescence, immunohistochemical staining, and western blot, respectively. We found that 2-week myopic induction can elevate PIK3R3 and AKT2 levels and activate the PI3K/Akt signaling pathway, enhance the expression of E-cadherin and matrix metallopeptidase 2 (MMP2), and decrease the level of transforming growth factor-beta 1 (TGF-β1), tissue inhibitor of matrix metalloproteinase-2 (TIMP2), and collagen (COLI) in the scleral tissue of myopic guinea pigs, thereby leading to scleral remolding. However, 4-week myopic induction could inhibit the PI3K/AKT signaling pathway and induce apoptosis, accompanied by increased MMP2, E-cadherin, and decreased TGF-β1, TIMP2, and COLI. Results reveal that the disturbed PI3K/AKT signaling plays a role in scleral remodeling in the experimental myopia through orchestrating apoptosis.
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