Literature DB >> 8804116

The concept of microglia in relation to central nervous system disease and regeneration.

S Moore1, S Thanos.   

Abstract

In a relatively short period of time, the microglial cell has gone from a strongly contested component of the central nervous system (CNS), to being recognised as one of the main players in the response to brain injury. Microglia are thought to arise from cells of haematopoietic origin, and enter the brain in response to naturally occurring cell death. As a result, the microglial cell is the representative of the immune system within the brain. However, the main role of microglia in the adult CNS is to respond to disruption of the homeostasis of the brain, whether that disruption comes from direct damage to neurons, neuronal degeneration or through disease. In this paper we investigate three main causes of cell death in the CNS: inherited degeneration, traumatic lesions and human diseases, and the microglial response to each. Then we examine the mechanisms by which microglia control their surroundings and the methods employed by these cells to instigate neuronal death. Recent observations suggest that under no conditions where neurons are dying or regrowing are microglia not involved, and control of microglia is likely to be just as important in regeneration as providing a favourable environment for neurons to grow. In short, microglia cannot be seen merely as cells of a certain type within the brain, possessing certain functions, but instead must be regarded as a concept that shapes the approaches taken to nervous system development, cell death, disease and trauma, and nervous system regeneration.

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Year:  1996        PMID: 8804116     DOI: 10.1016/0301-0082(95)00051-8

Source DB:  PubMed          Journal:  Prog Neurobiol        ISSN: 0301-0082            Impact factor:   11.685


  22 in total

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3.  Immunoproteasome responds to injury in the retina and brain.

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4.  RGMA and neogenin protein expression are influenced by lens injury following optic nerve crush in the rat retina.

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5.  Tenascin-R inhibits the growth of optic fibers in vitro but is rapidly eliminated during nerve regeneration in the salamander Pleurodeles waltl.

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6.  Expression of CD54 (intercellular adhesion molecule-1) and the beta 1 integrin CD29 is modulated by a cyclic AMP dependent pathway in activated primary rat microglial cell cultures.

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8.  Identification of a survival-promoting peptide in medium conditioned by oxidatively stressed cell lines of nervous system origin.

Authors:  T J Cunningham; L Hodge; D Speicher; D Reim; C Tyler-Polsz; P Levitt; K Eagleson; S Kennedy; Y Wang
Journal:  J Neurosci       Date:  1998-09-15       Impact factor: 6.167

9.  Upregulation of RANTES gene expression in neuroglia by Japanese encephalitis virus infection.

Authors:  Chun-Jung Chen; Jian-Hong Chen; Shih-Yun Chen; Su-Lan Liao; Shue-Ling Raung
Journal:  J Virol       Date:  2004-11       Impact factor: 5.103

10.  Tenascin-R is antiadhesive for activated microglia that induce downregulation of the protein after peripheral nerve injury: a new role in neuronal protection.

Authors:  D N Angelov; M Walther; M Streppel; O Guntinas-Lichius; W F Neiss; R Probstmeier; P Pesheva
Journal:  J Neurosci       Date:  1998-08-15       Impact factor: 6.167

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