基础医学与临床 ›› 2014, Vol. 34 ›› Issue (6): 828-833.

• 研究论文 • 上一篇    下一篇

小鼠脊髓损伤后周细胞促进脊髓血管新生

荆瀛黎1,武清斌2,苑晓晨1,3,李炳蔚4,刘明明4,张晓艳1,刘淑英1,李宏伟4,修瑞娟4   

  1. 1. 中国医学科学院北京协和医学院微循环研究所
    2. 中国医学科学院&北京协和医学院 微循环研究所
    3.
    4. 中国医学科学院微循环研究所
  • 收稿日期:2014-04-03 修回日期:2014-04-14 出版日期:2014-06-05 发布日期:2014-05-26
  • 通讯作者: 修瑞娟 E-mail:xiurj@aliyun.com
  • 基金资助:
    北京协和医学院研究生创新基金

Pericyte mediated angiogenesis in spinal cord injury mice

  • Received:2014-04-03 Revised:2014-04-14 Online:2014-06-05 Published:2014-05-26

摘要: 目的 探讨脊髓损伤后周细胞对微血管的影响。方法 C57BL/6小鼠随机分为:假手术组、损伤后2、7和14 d组(S2、S7和S14),每组9只。损伤组采用改良 Allen’s 法制作中度脊髓损伤模型。给小鼠颈静脉注入番茄凝集素(LEA),检测灌注微血管面积;用免疫荧光和免疫组化检测微血管面积和数目;用免疫荧光检测周细胞覆盖率。用缺氧条件(95% N2,5% CO2)模拟脊髓损伤的病理条件,用基质胶系统检测内皮细胞成管。结果 与假手术组相比,S2组灌注血管面积,微血管面积和数目显著降低(P < 0.001)。与S2组相比,S7组微血管数目和面积显著增高(P < 0.05);S14组灌注血管面积、微血管数目和面积均显著增高(P < 0.05, P < 0.01),但平均值仍低于假手术组。与假手术组相比,S2和S7组周细胞覆盖率持续下降(P < 0.001)。周细胞与内皮细胞共培养可显著增加缺氧条件下内皮细胞成管长度(P < 0.01)。结论 脊髓损伤后周细胞可促进脊髓血管新生。

关键词: 周细胞, 脊髓损伤, 血管新生

Abstract: Objective The aim of our study was to investigate the influence of pericytes on microvascular angiogenesis after spinal cord injury (SCI). Methods C57BL/6 mice were randomly divided into four groups: sham group, 2 days (S2), 7 days (S7) and 14 days after SCI group (S14) (n=9 per group). The injury group received a moderate impacted spinal cord injury. Perfused blood vessels were detected by FITC-LEA intravenous injection; microvessel area density (MVA) and microvessel density (MVD) were analyzed by immunofluorescence and immunohistochemistry, respectively; pericyte coverage was further calculated by immunofluorescence. Hypoxic condition (95% N2 and 5% CO2) was applied to mimic the phathological situation of SCI, endothelial tubular formation was detected by matrigel system. Results The area of perfused blood vessels, MVA and MVD at S2 were significantly decreased compared with that at sham (P < 0.001). MVA and MVD at S7 was notably increased compared with that at S2 (P < 0.05). The area of perfused blood vessels, MVA and MVD at S14 showed a markedly increase compared with that at S2 (P < 0.05, P < 0.01), which were still lower than that at sham. Pericyte coverage was decreased at S2 and S7 in mice compared with sham control. Co-culture of pericytes and endothelial cells (ECs) could markedly increase endothelia tube length compared with ECs alone under hypoxia (P < 0.01). Conclusion Pericytes might promote angiogenesis in spinal cord injury C57BL/6 mice.

Key words: pericyte, spinal cord injury, angiogenesis

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