期刊
GLIA
卷 56, 期 15, 页码 1691-1709出版社
WILEY-BLACKWELL
DOI: 10.1002/glia.20721
关键词
reactive astrocyte; astrogliosis; neurite outgrowth; inhibition; proteoglycans; tenascin; CNS injury; spinal cord injury; meningeal cells; fibroblast
资金
- Paralyzed Veteran's Association
- Christopher Reeve Paralysis Foundation
- Buoniconti Fund
Astrocytes respond to central nervous system (CNS) injury with reactive astrogliosis and participate in the formation of the glial sear, an inhibitory barrier for axonal regeneration. Little is known about the injury-induced mechanisms underlying astrocyte reactivity and subsequent development of an axon-inhibitory sear. We combined two key aspects of CNS injury, mechanical trauma and co-culture with meningeal cells, to produce an in vitro model of the scar from cultures of highly differentiated astrocytes. Our model displayed widespread morphological signs of astrocyte reactivity, increases in expression of glial fibrillary acidic protein (GFAP), and accumulation of GFAP in astrocytic processes. Expression levels of scar-associated markers, phosphacan, neurocan, and tenascins, were also increased. Importantly, neurite growth from various CNS neuronal populations was significantly reduced when neurons were seeded on the scar-like cultures, compared with growth on cultures of mature astrocytes. Quantification of neurite growth parameters on the scar model demonstrated significant reductions in neuronal adhesion and neurite lengths. Interestingly, neurite outgrowth of postnatal neurons was reduced to a greater extent than that of embryonic neurons, and outgrowth inhibition varied among neuronal populations. Scar-like reactive sites and neurite-inhibitory patches were found throughout these cultures, creating a patchwork of growth-inhibitory areas mimicking a CNS injury site. Thus, our model showed relevant aspects of scar formation and produced widespread inhibition of axonal regeneration; it should be useful both for examining mechanisms underlying scar formation and to assess various treatments for their potential to improve regeneration after CNS injury. (C) 2008 Wiley-Liss, Inc.
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