Department of Physical Medicine and Rehabilitation, University of Alabama at Birmingham, Birmingham, Alabama, USA.
J Neurochem. 2010 Nov;115(4):864-72. doi: 10.1111/j.1471-4159.2010.06770.x.
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 17β-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.
施万细胞(Schwann cell,SC)移植是脊髓损伤(spinal cord injury,SCI)后一种很有前途的修复策略;然而,大量的 SC 在移植后无法存活。先前的研究表明,17β-雌二醇(17β-estradiol,E2)可保护多种细胞类型免受细胞毒性。因此,本研究评估了 E2 对体外 SC 的保护潜力,并研究了 E2 对 SCI 大鼠模型中移植 SC 存活的影响。发现原代 SC 培养物强烈表达雌激素受体(estrogen receptor,ER),用 E2 孵育可保护 SC 免受过氧化氢诱导的细胞死亡。这种保护不受 ER 拮抗剂 ICI 182,780 的抑制,表明基因组信号对于保护不是必需的。在随后的实验中,雄性大鼠进行颈半脱位 SCI 诱导,然后持续给予 E2 或安慰剂。SCI 后 8 天,将 SC 移植到损伤中心。E2 治疗显著增加了移植后 7 天评估的存活标记的移植 SC 数量。这些数据表明,E2 可保护 SC 免受氧化应激,并提高移植 SC 的存活率,这表明 E2 给药可能是增强 SCI 后移植 SC 存活的一种干预措施。