中国神经再生研究(英文版) ›› 2017, Vol. 12 ›› Issue (11): 1885-1894.doi: 10.4103/1673-5374.219051

• 原著:脊髓损伤修复保护与再生 • 上一篇    下一篇

胸段脊髓损伤后远端神经前体细胞而非星形胶质细胞响应损伤

  

  • 收稿日期:2017-09-22 出版日期:2017-11-15 发布日期:2017-11-15
  • 基金资助:

    美国UTS基金

Neural progenitor cells but not astrocytes respond distally to thoracic spinal cord injury in rat models

Tara Nguyen, Yilin Mao, Theresa Sutherland, Catherine Anne Gorrie   

  1. School of Life Sciences, Faculty of Science, University of Technology Sydney, New South Wales, Australia
  • Received:2017-09-22 Online:2017-11-15 Published:2017-11-15
  • Contact: Catherine Anne Gorrie, Ph.D.,Catherine.gorrie@uts.edu.au.
  • Supported by:

    This study was supported by UTS Faculty of Science Early Career Research Grant to CAG.

摘要:

我们前期研究已经发现,创伤性中枢神经系统损伤后,人脊髓中巢蛋白阳性细胞被广泛激活。我们感兴趣的是对局部脊髓损伤后,沿神经轴远端细胞反应情况。为了研究了胸段脊髓损伤后贯穿神经轴的内源性神经前体细胞、非星形胶质细胞和小胶质细胞反应。成年雌性SD大鼠随机分为胸段脊髓挫伤组(n = 9),假手术组(n = 8)和未进行手术的对照组(n = 8)。损伤后24h对脊髓和脑组织神经轴的6个区域进行固定和切片。免疫组织化学显示在脊髓所有水平有中央管均可见神经前体细胞的标志物巢蛋白免疫反应性增加,活化小胶质细胞的数量在损伤部位显著增加并延伸至腰膨大部,而星形胶质细胞特异性标志物胶质纤维酸性蛋白免疫反应仅在损伤区中心可见。3组大鼠第三脑室的巢蛋白、胶质纤维酸性蛋白、小胶质细胞反应均无变化。这些研究结果表明,脊髓损伤后神经前体细胞,星形胶质细胞和小胶质细胞反应在神经轴各水平存在差异,这一结果将为中枢神经系统疾病治疗时考虑如何控制某类细胞群奠定基础。

orcid:0000-0001-5934-2492(Catherine Anne Gorrie)

关键词: 神经再生, 脊髓损伤, 室管膜细胞, 胶质纤维酸性蛋白, 小胶质细胞, 巢蛋白, 神经轴, 脑室膜细胞

Abstract:

Traumatic spinal cord injury (SCI) is a detrimental condition that causes loss of sensory and motor function in an individual. Many complex secondary injury cascades occur after SCI and they offer great potential for therapeutic targeting. In this study, we investigated the response of endogenous neural progenitor cells,astrocytes, and microglia to a localized thoracic SCI throughout the neuroaxis. Twenty-five adult female Sprague-Dawley rats underwent mild-contusion thoracic SCI (n = 9), sham surgery (n = 8), or no surgery (n = 8). Spinal cord and brain tissues were fixed and cut at six regions of the neuroaxis. Immunohistochemistry showed increased reactivity of neural progenitor cell marker nestin in the central canal at all levels of the spinal cord. Increased reactivity of astrocyte-specific marker glial fibrillary acidic protein was found only at the lesion epicenter. The number of activated microglia was significantly increased at the lesion site,and activated microglia extended to the lumbar enlargement. Phagocytic microglia and macrophages were significantly increased only at the lesion site. There were no changes in nestin, glial fibrillary acidic protein,microglia and macrophage response in the third ventricle of rats subjected to mild-contusion thoracic SCI  compared to the sham surgery or no surgery. These findings indicate that neural progenitor cells, astrocytes and microglia respond differently to a localized SCI, presumably due to differences in inflammatory signaling.These different cellular responses may have implications in the way that neural progenitor cells can be manipulated for neuroregeneration after SCI. This needs to be further investigated.

Key words: nerve regeneration, contusion, spinal cord, neuroinflammatory, ependymal cell, glial fibrillary acidic protein, microglia, nestin, neuroaxis, tanycyte, third ventricle, trauma, neural regeneration