role of gap junction protein connexin43 in astrogliosis induced by brain injury角色的缝隙连接蛋白connexin43 astrogliosis引起的脑损伤.pdfVIP
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role of gap junction protein connexin43 in astrogliosis induced by brain injury角色的缝隙连接蛋白connexin43 astrogliosis引起的脑损伤
Role of Gap Junction Protein Connexin43 in Astrogliosis
Induced by Brain Injury
Nicolas Theodoric, John F. Bechberger, Christian C. Naus, Wun-Chey Sin*
Department of Cellular and Physiological Sciences, Life Sciences Institute, The University of British Columbia, Vancouver, British Columbia, Canada
Abstract
Astrogliosis is a process that involves morphological and biochemical changes associated with astrocyte activation in
response to cell damage in the brain. The upregulation of intermediate filament proteins including glial fibrillary acidic
protein (GFAP), nestin and vimentin are often used as indicators for astrogliosis. Although connexin43 (Cx43), a channel
protein widely expressed in adult astrocytes, exhibits enhanced immunoreactivity in the peri-lesion region, its role in
astrogliosis is still unclear. Here, we correlated the temporal and spatial expression of Cx43 to the activation of astrocytes
and microglia in response to an acute needle stab wound in vivo. We found large numbers of microglia devoid of Cx43 in
the needle wound at 3 days post injury (dpi) while reactive astrocytes expressing Cx43 were present in the peripheral zone
surrounding the injury site. A redistribution of Cx43 to the needle site, corresponding to the increased presence of GFAP-
positive reactive astrocytes in the region, was only apparent from 6 dpi and sustained until at least 15 dpi. Interestingly, the
extent of microglial activation and subsequent astrogliosis in the brain of Cx43 knockout mice was significantly larger than
those of wild type, suggesting that Cx43 expression limits the degree of microgliosis. Although Cx43 is not essential for
astrogliosis and microglial activation induced by a needle injury, our results demonstrate that Cx43 is a useful marker for
injury induced astrogliosis due to its enhanced expression specifically within a sma
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