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氧化预处理促进骨髓间充质干细胞迁移并防止其凋亡。

Oxidative preconditioning promotes bone marrow mesenchymal stem cells migration and prevents apoptosis.

作者信息

Li ShiYong, Deng YuBin, Feng JianQiang, Ye WeiBiao

机构信息

Department of Pathophysiology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, China.

出版信息

Cell Biol Int. 2009 Mar;33(3):411-8. doi: 10.1016/j.cellbi.2009.01.012. Epub 2009 Jan 24.

Abstract

Reactive oxygen species (ROS) play essential roles in apoptosis and in the regulation of several transcription factors under both physiological and pathological conditions. However, the effects of ROS on MSCs are not well known, and therefore we have investigated the effects of preconditioning with hydrogen peroxide (H(2)O(2)) on the level of expression of the chemokine receptor, CXCR4, stromal cell-derived factor-1alpha (SDF-1alpha)-dependent migration and apoptosis in MSCs. Preconditioning with 20microM H(2)O(2) significantly increased the level of expression of CXCR4 mRNA and protein, and MSCs migration toward SDF-1alpha; increased expression of CXCR4 and SDF-1alpha-induced MSCs migration was attenuated by extracellular signal-regulated kinase (ERK) inhibitor PD98059. Preconditioning with 20microM H(2)O(2) significantly protected MSCs against apoptosis induced by 500microM H(2)O(2). These results suggest that preconditioning with H(2)O(2) can increase MSCs migration toward SDF-1alpha and protect MSCs against apoptosis.

摘要

活性氧(ROS)在生理和病理条件下的细胞凋亡以及多种转录因子的调控中发挥着重要作用。然而,ROS对间充质干细胞(MSCs)的影响尚不明确,因此我们研究了用过氧化氢(H₂O₂)预处理对趋化因子受体CXCR4的表达水平、基质细胞衍生因子-1α(SDF-1α)依赖的MSCs迁移以及MSCs凋亡的影响。用20μM H₂O₂预处理显著增加了CXCR4 mRNA和蛋白的表达水平,以及MSCs向SDF-1α的迁移;细胞外信号调节激酶(ERK)抑制剂PD98059减弱了CXCR4表达增加和SDF-1α诱导的MSCs迁移。用20μM H₂O₂预处理显著保护MSCs免受500μM H₂O₂诱导的凋亡。这些结果表明,用H₂O₂预处理可增加MSCs向SDF-1α的迁移并保护MSCs免受凋亡。

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