Protective Role of Bone Marrow Mesenchymal Stem Cells (BMSCs) in Repairing Epithelial Cells of Diabetic Retinopathy

被引:0
作者
Ling, Yu [1 ]
Liang, Haiming [1 ]
Tang, Qi [1 ]
机构
[1] Guangxi Med Univ, Affiliated Hosp 5, Peoples Hosp Nanning 1, Dept Ophthalmol, Nanning 530022, Guangxi, Peoples R China
关键词
Epithelial Cells; Bone Marrow Mesenchymal Stem Cells; PI3K; Akt Signal; Transduction Pathway; Inflammatory Damage; DRY EYE; AUTOPHAGY;
D O I
10.1166/jbt.2022.3133
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Diabetic retinopathy (DR) is one of the main causes of blindness. By directly employing mesenchy-mal stem cells to repair damaged retinal tissues, we aim to study the underlying repair mechanisms. 30 DR patients were included, along with 30 healthy control cases. Western-blot and qRT-PCR were conducted to measure PI3K/Akt pathway-related genes. The PI3K/Akt antagonist (Rigosertib) was utilized in the induction process of cell differentiation to analyze the effects of PI3K/Akt pathway -specific proteins and mRNAs. DR patients showed significantly elevated expression of PI3K/Akt compared to control. With prolongation of induction, the expression of normal epithelial cell-related genes (SpC, SpB, SpA, CK18, KGF and Occludin) was elevated along with upregulated Occludin and KGF, two specific proteins of healthy epithelial cells. Meanwhile, the quantities of Occludin and KGF in cell culture medium showed a gradual downward trend. In the differentiation of BMSCs towards epithelial cells, addition of PI3K/Akt antagonist Rigosertib was negatively correlated with the expression of several genes (IGF-1, shh, EGF, mTOR, AKT and PI3K) and decreased the quantities of PI3K/Akt pathway-specific proteins (mTOR, PI3K and AKT).In conclusion, BMSCs can effectively IP: 182.75.148.10 On: Sat, 20 Aug 2022 10:37:17 reduce the release of cytokines in DR and promote the repair of damaged diabetic retina, possibly Copyright: American Scientific Publishers through regulation of PI3K/Akt signaling pathway. Delivered by Ingenta
引用
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页码:2100 / 2105
页数:6
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