中国神经再生研究(英文版) ›› 2015, Vol. 10 ›› Issue (6): 944-950.doi: 10.4103/1673-5374.158359

• 原著:神经损伤修复保护与再生 • 上一篇    下一篇

幼年短暂性全脑缺血海马神经元延迟死亡与p63表达相关

  

  • 收稿日期:2015-02-18 出版日期:2015-06-18 发布日期:2015-06-18
  • 基金资助:

    韩国科学、ICT和未来计划部国家基础科学研究项目(NRF-2014R1A2A2A01005307);韩国教育部国家基础研究项目(NRF-2014R1A6A3A01056005)

Delayed hippocampal neuronal death in young gerbil following transient global cerebral ischemia is related to higher and longer-term expression of p63 in the ischemic hippocampus

Eun Joo Bae 1, Bai Hui Chen 2, Bing Chun Yan 3, Bich Na Shin 2, Jeong Hwi Cho 4, In Hye Kim 4, Ji Hyeon Ahn 4, Jae Chul Lee 4, Hyun-Jin Tae 5, Seongkweon Hong 6, Dong Won Kim 7, 8, Jun Hwi Cho 8, Yun Lyul Lee 2, Moo-Ho Won 4, Joon Ha Park 4   

  1. 1 Department of Pediatrics, Chuncheon Sacred Heart Hospital, College of Medicine, Hallym University, Chuncheon, South Korea
    2 Department of Physiology, College of Medicine, Institute of Neurodegeneration and Neuroregeneration, Hallym University, Chuncheon, South Korea
    3 Institute of Integrative Traditional & Western Medicine, Medical College, Yangzhou University, Yangzhou, Jiangsu Province, China
    4 Department of Neurobiology, School of Medicine, Kangwon National University, Chuncheon, South Korea
    5 Department of Biomedical Science and Research Institute for Bioscience and Biotechnology, Hallym University, Chunchon, South Korea
    6 Department of Surgery, School of Medicine, Kangwon National University, Chuncheon, South Korea
    7 Department of Emergency Medicine, Chuncheon Sacred Heart Hospital, College of Medicine, Hallym University, Chuncheon, South Korea
    8 Department of Emergency Medicine, School of Medicine, Kangwon National University, Chuncheon, South Korea
  • Received:2015-02-18 Online:2015-06-18 Published:2015-06-18
  • Contact: Moo-Ho Won, D.V.M., Ph.D. or Joon Ha Park, Ph.D., mhwon@kangwon.ac.kr or parkfamilyda@hanmail.net.
  • Supported by:

     This study was supported by 2013 Research Grant from Kangwon National University (120131480), and Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (NRF-2014R1A6A3A01056005).

摘要:

p53在脑缺血大脑中的变化已有报道,但其家族成员肿瘤抑制因子p63在全脑缺血海马中的表达变化研究报道较少。为此,实验比较了幼年(鼠龄1个月)和成年(鼠龄6个月)经历5min短暂性全脑缺血后海马CA1-3区p63的表达。发现幼年沙鼠海马CA1区神经元死亡的发生较成年沙鼠延迟。成年沙鼠海马CA1区锥体神经元p63免疫反应在缺血后4d明显降低,且明显低于幼年沙鼠。缺血后7d,成年和幼年沙鼠海马CA1区锥体神经元p63免疫反应均减弱,p63蛋白表达在幼年和成年沙鼠海马CA1区随缺血时间的变化与其免疫反应相似。说明幼年相较于成年海马CA1区神经元死亡延迟的原因,与p63表达在较长时间内维持较高水平有关。

关键词: p53, 脑缺血再灌注, 海马, CA1区, 锥体神经元, 延迟性神经元死亡, 免疫组化, 免疫印迹

Abstract:

The tumor suppressor p63 is one of p53 family members and plays a vital role as a regulator of neuronal apoptosis in the development of the nervous system. However, the role of p63 in mature neuronal death has not been addressed yet. In this study, we first compared ischemia-induced effects on p63 expression in the hippocampal regions (CA1–3) between the young and adult gerbils subjected to 5 minutes of transient global cerebral ischemia. Neuronal death in the hippocampal CA1 region of young gerbils was significantly slow compared with that in the adult gerbils after transient global cerebral ischemia. p63 immunoreactivity in the hippocampal CA1 pyramidal neurons in the sham-operated young group was significantly low compared with that in the sham-operated adult group. p63 immunoreactivity was apparently changed in ischemic hippocampal CA1 pyramidal neurons in both ischemia-operated young and adult groups. In the ischemia-operated adult groups, p63 immunoreactivity in the hippocampal CA1 pyramidal neurons was significantly decreased at 4 days post-ischemia; however, p63 immunoreactivity in the ischemia-operated young group was significantly higher than that in the ischemia-operated adult group. At 7 days post-ischemia, p63 immunoreactivity was decreased in the hippocampal CA1 pyramidal neurons in both ischemia-operated young and adult groups. Change patterns of p63 level in the hippocampal CA1 region of adult and young gerbils after ischemic damage were similar to those observed in the immunohistochemical results. These findings indicate that higher and longer-term expression of p63 in the hippocampal CA1 region of the young gerbils after ischemia/reperfusion may be related to more delayed neuronal death compared to that in the adults.

Key words: p53 tumor suppressor gene family, cerebral ischemia/reperfusion, pyramidal neurons, CA1 region, delayed neuronal death, immunohistochemistry, western blotting, neural regeneration