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Human placenta-derived mesenchymal stem cells trigger repair system in TAA-injured rat model via antioxidant effect

机译:人胎盘衍生的间充质干细胞通过抗氧化作用引发TAA损伤大鼠模型的修复系统

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摘要

Oxidative stress induces damages of various cell types or tissues through a repetitive imbalance between the systemic manifestation of reactive oxygen species (ROS) and detoxification of the reactive intermediates. Thioacetamide (TAA) is well known for causing several degenerative diseases by oxidative stress. However, study of the antioxidant mechanisms of stem cells in TAA-injured rat model is insufficient. Therefore, we investigated the effect of placenta-derived mesenchymal stem cells (PD-MSCs) transplantation on liver and ovary of TAA-injured rat models to study the antioxidant effect in degenerative diseases. In TAA-injured rat model, PD-MSCs engrafted into damaged organ including liver and ovary in PD-MSCs transplanted groups (Tx) compared with non-transplanted groups (NTx) (*p<0.05). Transplanted PD-MSCs reduced inflammatory factors and upregulated oxidative stress factors in Tx compared with NTx (*p<0.05). Also, transplanted PD-MSCs enhanced antioxidants factors and organ functional restoration factors in Tx compared with NTx. These data show that PD-MSC transplantation triggers the regeneration of organ (e.g., liver and ovary) damaged by oxidative stress from TAA treatment via activating antioxidant factors. Therefore, these data suggest the therapeutic potential via antioxidant effect and help understand the therapeutic mechanism of PD-MSCs in damaged tissues such as in liver and reproductive system.
机译:氧化应激通过反应性氧(ROS)的全身表现与反应性中间体的解毒之间的重复性不平衡引起各种细胞类型或组织的损伤。迄今为止,硫代乙酰胺(TAA)众所周知,通过氧化应激引起几种退化性疾病。然而,对TaA损伤大鼠模型中干细胞抗氧化机制的研究不足。因此,我们研究了胎盘衍生的间充质干细胞(PD-MSCs)移植对TAA损伤大鼠模型的肝脏和卵巢的影响,以研究退行性疾病的抗氧化效果。在TAA损伤的大鼠模型中,与非移植基团(NTX)相比,PD-MSCs移植组(TX)中的PD-MSC植入受损的器官,包括肝脏和卵巢(TX)(* P <0.05)。与NTX相比,移植的PD-MSCs降低了TX中的炎症因子和上调氧化应激因子(* P <0.05)。此外,与NTX相比,移植的PD-MSC增强了抗氧化剂因子和器官功能恢复因子。这些数据显示PD-MSC移植触发通过激活抗氧化因子通过氧化应激受到氧化胁迫而受损的器官(例如肝脏和卵巢)的再生。因此,这些数据通过抗氧化作用表明治疗潜力,并有助于了解PD-MSCs在肝脏和生殖系统中受损组织中PD-MSC的治疗机制。

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