East, Emma; Golding, Jon and Phillips, James
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|DOI (Digital Object Identifier) Link:||https://doi.org/10.1089/ten.2007.1501|
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Injury to the spinal cord results in the formation of a glial scar which is associated with inhibition of axonal regeneration. One of the major limitations of research into improving repair strategies is the lack of a cell culture model that accurately recapitulates the complex in vivo situation. Our aim is to develop an effective model to address this need.
Astrocytes in the undamaged CNS express low levels of GFAP, but following injury exhibit a reactive phenotype exemplified by GFAP up-regulation. Primary glial cell cultures were analysed in 2D monolayers and 3D collagen gels for GFAP expression. In 2D cultures 73.4 ± 4.0% of cells were GFAP positive, whereas 40.7 ± 3.5% were immunoreactive for GFAP in 3D collagen gels. As 3D astrocyte cultures more closely modelled the in vivo situation we used this model to investigate the response of astrocytes to dorsal root ganglia cells (DRGs). Dissociated DRGs were labelled with CellTrackerTM, seeded onto astrocyte-populated collagen gels and maintained in culture for 5 days. Astrocytes near the DRG interface showed marked GFAP up-regulation and adopted a reactive morphology which was observed up to 1mm away.
Astrocytes in 3D culture exhibit a lower basal level of reactivity than cells grown in monolayer, providing a system in which stimulation of activation can be investigated. This model provides a useful tool for investigating triggers of reactive gliosis, as demonstrated by the response observed to cells found at the inhibitory interfaces formed following damage to the spinal cord.
|Item Type:||Conference Item|
|Academic Unit/School:||Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM)
|Interdisciplinary Research Centre:||Biomedical Research Network (BRN)|
|Depositing User:||James Phillips|
|Date Deposited:||25 Sep 2007|
|Last Modified:||01 Feb 2017 12:09|
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