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Transgenic models for cytokine-induced neurological disease

期刊

出版社

ELSEVIER
DOI: 10.1016/j.bbadis.2009.10.004

关键词

Central nervous system; Cytokine; Interferon; Interleukin-6; Interleukin-12; Neurological disease; Transgenic mouse; Transforming growth factor-beta

资金

  1. National Institutes of Health [MH50426, MH62231, NS036979]
  2. National Health and Medical Research Council of Australia [512407]
  3. New South Wales Government
  4. Deutsche Forschungsgemeinschaft through a postdoctoral fellowship [DFG HO3298/1-1]
  5. [DFG PA602/2]
  6. [BMBF 01 KI 9951]
  7. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH050426, R01MH062231] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS036979] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Considerable evidence supports the idea that cytokines are important mediators of pathophysiologic processes within the central nervous system (CNS). Numerous studies have documented the increased production of various cytokines in the human CNS in a variety of neurological and neuropsychiatric disorders. Deciphering cytokine actions in the intact CNS has important implications for our understanding of the pathogenesis and treatment of these disorders. One approach to address this problem that has been used widely employs transgenic mice with CNS-targeted production of different cytokines. Transgenic production of cytokines in the CNS of mice allows not only for the investigation of complex cellular responses at a localized level in the intact brain but also more closely recapitulates the expression of these mediators as found in disease states. As discussed in this review, the findings show that these transgenic animals exhibit wide-ranging structural and functional deficits that are linked to the development of distinct neuroinflammatory responses which are relatively specific for each cytokine. These cytokine-induced alterations often recapitulate those found in various human neurological disorders not only underscoring the relevance of these models but also reinforcing the clinicopathogenetic significance of cytokines in diseases of the CNS. (C) 2009 Elsevier B.V. All rights reserved.

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