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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >17beta-estradiol protects Schwann cells against H2O2-induced cytotoxicity and increases transplanted Schwann cell survival in a cervical hemicontusion spinal cord injury model.
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17beta-estradiol protects Schwann cells against H2O2-induced cytotoxicity and increases transplanted Schwann cell survival in a cervical hemicontusion spinal cord injury model.

机译:17β-雌二醇可保护Schwann细胞免受H2O2诱导的细胞毒性作用,并在子宫颈半截瘫脊髓损伤模型中提高已移植的Schwann细胞存活率。

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摘要

Schwann cell (SC) transplantation is a promising repair strategy after spinal cord injury (SCI); however, a large number of SCs do not survive following transplantation. Previous studies have shown that 17beta-estradiol (E2) protects several cell types against cytotoxicity. Thus, this study evaluated the protective potential of E2 on SCs in vitro and investigated the effect of E2 on transplanted SC survival in a rat model of SCI. Primary SC cultures were found to robustly express estrogen receptors (ER) and incubation with E2 protected SCs against hydrogen peroxide-induced cell death. This protection was not inhibited by the ER antagonist ICI 182,780, suggesting that genomic signaling is not necessary for protection. In a subsequent experiment, cervical hemicontusion SCI was induced in male rats followed by sustained administration of E2 or placebo. Eight days after SCI, SCs were transplanted into the injury epicenter. E2 treatment significantly increased the number of surviving labeled transplanted SCs evaluated 7 days after transplantation. These data demonstrate that E2 protects SCs against oxidative stress and improves transplanted SC survival, which suggests that E2 administration may be an intervention of choice for enhancing survival of transplanted SCs after SCI.
机译:雪旺细胞(SC)移植是脊髓损伤(SCI)后有希望的修复策略。然而,大量的SC在移植后不能存活。先前的研究表明17β-雌二醇(E2)保护几种细胞免受细胞毒性作用。因此,本研究评估了E2在体外对SC的保护潜力,并研究了E2对SCI大鼠模型中移植的SC存活的影响。发现原代SC培养物能强烈表达雌激素受体(ER),并与E2保护的SC一起孵育,以防止过氧化氢诱导的细胞死亡。 ER拮抗剂ICI 182,780并未抑制这种保护作用,这表明基因组信号传导对于保护不是必需的。在随后的实验中,在雄性大鼠中诱发宫颈半截肌SCI,然后持续给予E2或安慰剂。 SCI八天后,将SC移植到损伤中心。 E2处理显着增加了移植后7天评估的存活标记移植SC的数量。这些数据表明,E2保护SC免受氧化应激并改善移植的SC生存,这表明E2给药可能是增强SCI后移植的SC生存的选择干预措施。

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