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人胎盘源间充质干细胞通过抗氧化作用触发 TAA 损伤大鼠模型中的修复系统。

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

机构信息

Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.

Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA 92093, USA.

出版信息

Aging (Albany NY). 2020 Dec 26;13(1):61-76. doi: 10.18632/aging.202348.

Abstract

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) (<0.05). Transplanted PD-MSCs reduced inflammatory factors and upregulated oxidative stress factors in Tx compared with NTx (<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.

摘要

氧化应激通过活性氧(ROS)系统表现与活性中间体解毒之间的反复失衡,导致各种细胞类型或组织损伤。硫代乙酰胺(TAA)是众所周知的通过氧化应激引起多种退行性疾病的物质。然而,关于 TAA 损伤大鼠模型中干细胞抗氧化机制的研究还不够充分。因此,我们研究了胎盘间充质干细胞(PD-MSCs)移植对 TAA 损伤大鼠模型肝脏和卵巢的影响,以研究退行性疾病中的抗氧化作用。在 TAA 损伤大鼠模型中,与非移植组(NTx)相比,PD-MSCs 移植组(Tx)的受损器官(包括肝脏和卵巢)中出现了 PD-MSCs(<0.05)。与 NTx 相比,Tx 中的移植 PD-MSCs 降低了炎症因子并上调了氧化应激因子(<0.05)。此外,与 NTx 相比,Tx 中的移植 PD-MSCs 增强了抗氧化因子和器官功能恢复因子。这些数据表明,PD-MSC 移植通过激活抗氧化因子,触发了 TAA 处理引起的氧化应激损伤的器官(如肝脏和卵巢)的再生。因此,这些数据表明通过抗氧化作用的治疗潜力,并有助于理解 PD-MSCs 在受损组织(如肝脏和生殖系统)中的治疗机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dfd/7835021/3f5e96428afe/aging-13-202348-g001.jpg

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