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Protective effect of melatonin on bone marrow mesenchymal stem cells against hydrogen peroxide-induced apoptosis in vitro

机译:褪黑素对骨髓间充质干细胞的抗过氧化氢诱导的体外凋亡的保护作用

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Bone marrow mesenchymal stem cells (MSCs) transplantation has shown great promises for treating various central nervous system (CNS) diseases. However, poor viability of transplanted MSCs in injured CNS has limited the therapeutic efficiency. Oxidative stress is one of major mechanisms underlying the pathogenesis of CNS diseases and has a negative impact on the survival of transplanted MSCs. Melatonin has recently been reported to have the antioxidant and anti-apoptotic properties in serial of cells. This study was designed to investigate the protective effect and potential mechanisms of melatonin against hydrogen peroxide (H2O2)-induced apoptosis of MSCs. MSCs were pretreated with melatonin (1, 10, and 100 nM, respectively) for 30 min, followed by exposure to 400 μM H2O2 and melatonin together for 12 h. The present study reports that melatonin pretreatment significantly attenuated H2O2-induced MSC apoptosis in a dose-dependent manner. Consistently, melatonin effectively suppressed the generation of intracellular ROS, expression ratio of Bax/Bcl-2, activation of caspase-3 and expression of phospho-P38MAPK in H2O 2-induced MSCs. Luzindole, a nonselective melatonin receptor antagonist, significantly counteracted melatonin's promotion effect on cell survival, indicating that melatonin exerts its protective effect on MSCs, at least in part, through the activation of melatonin receptors. The findings suggest that melatonin may be an effectively protective agent against oxidative stress-induced MSC apoptosis. J. Cell. Biochem. 114: 2346-2355, 2013.
机译:骨髓间充质干细胞(MSCs)移植已显示出治疗各种中枢神经系统(CNS)疾病的巨大希望。但是,移植的MSC在受损的CNS中的生存力较差,限制了治疗效率。氧化应激是中枢神经系统疾病发病机理的主要机制之一,并且对移植的MSC的存活具有负面影响。最近已经报道褪黑激素在一系列细胞中具有抗氧化和抗凋亡特性。本研究旨在探讨褪黑素对过氧化氢(H2O2)诱导的MSCs凋亡的保护作用及其潜在机制。用褪黑激素(分别为1、10和100 nM)对MSC进行30分钟预处理,然后将其与400μMH2O2和褪黑素一起暴露12 h。本研究报道褪黑素预处理以剂量依赖性方式显着减弱了H2O2诱导的MSC凋亡。一致地,褪黑素有效地抑制了H2O 2诱导的MSC中细胞内ROS的生成,Bax / Bcl-2的表达比例,caspase-3的激活以及磷酸化P38MAPK的表达。非选择性褪黑激素受体拮抗剂Luzindole显着抵消了褪黑激素对细胞存活的促进作用,表明褪黑激素至少部分地通过激活褪黑激素受体发挥了其对MSC的保护作用。这些发现提示褪黑激素可能是抗氧化应激诱导的MSC凋亡的有效保护剂。 J.细胞。生化。 114:2346-2355,2013。

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