Repository logo
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
Repository logo
    Communities & Collections
    Research Outputs
    Fundings & Projects
    People
    Organizations
    Statistics
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. Administrative Units/行政單位
  3. School History Room/校史室
  4. 校院出版品
  5. 中山醫學雜誌
  6. 小白鼠感染廣東住血線蟲誘發基質金屬蛋白9與小腦浦金氏細胞喪失之關係
 
  • Details
Options

小白鼠感染廣東住血線蟲誘發基質金屬蛋白9與小腦浦金氏細胞喪失之關係

Journal Volume
中山醫學雜誌
Journal Issue
v14 n.4 p485-493
Date Issued
2010-07-28T09:23:54Z
URI
https://scholars.csmu.edu.tw/handle/123456789/8794
Abstract
廣東住血線蟲症(angiostrongyliasis)引起之神經系統疾病是由於發育中的廣東住血線蟲(Angiostrongylus cantonensis)侵入中樞神經系統所造成。在感染廣東住血線蟲的BALB/c strain小白鼠發現小腦浦金氏(Purkinje)細胞出現退化性萎縮及部分喪失的現象。基質金屬蛋白9(matrix metalloproteinase-9,MMP-9)mRNA的表現及酵素活性只在感染廣東住血線蟲的小白鼠小腦檢測到,經西方點墨法(Western blotting)確定此酵素為MMP-9,而在未感染的小白鼠則檢測不到此酵素。另外,組織免疫試驗亦證實MMP-9定位在退化的浦金氏細胞。這些結果顯示MMP-9可能與小白鼠感染廣東住血線蟲引起小腦浦金氏細胞喪失有關。
Neurological disorders in angiostrongyliasis are caused by invasion of the central nervous system by developing Angiostrongylus cantonensis larvae. After A. cantonensis infection, the cerebellums of BALB/c strain mice were observed to have a loss of Purkinje cells. Histologically, the Purkinje cells in the infected mice cerebellum were shown to have degenerative atrophy or partial loss. The matrix metalloproteinase-9 (MMP-9) mRNA and activity was induced in the infected mice, and the enzyme was absent in uninfected mice. Western blotting showed that the anti-MMP-9 antibody recognized a single 94 kDa protein from A. cantonensis-infected mice. Immunohistochemistry also showed localization of MMP-9 within the degenerative Purkinje cells. These results suggest MMP-9 in mice infected with A. cantonensis may be related to the loss of Purkinje cells.
Make it your own

DSpace-CRIS can be extensively configured to meet your needs. Decide which information need to be collected and available with fine-grained security. Start updating the theme to match your Institution's web identity.

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science

  • Cookie settings
  • Privacy policy
  • End User Agreement
  • Send Feedback