| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2167145 | Cellular Immunology | 2013 | 9 Pages |
Characteristics of myelin basic protein (MBP)-induced experimental autoimmune encephalomyelitis (EAE) include acute edema and infiltration of mononuclear cells (MNCs) in the microvessels of central nervous system (CNS). Aquaporin-4 (AQP4) is a water channel protein expressed in astrocytes foot process throughout the CNS. We performed immunostaining, western blotting and semi-quantitative real-time RT-PCR of AQP4 and glial fibrillary acidic protein (GFAP) in CNS from rats immunized with MBP. Immunohistochemical analysis revealed that AQP4 is down-regulated in MNCs infiltrated microvessels of rats with EAE. Furthermore, western blotting and real-time RT-PCR analyses showed that AQP4 was significantly decreased at the stage of severe EAE compared with control rats. On the other hand, expression of GFAP-protein was significantly increased after stage of severe EAE. Our findings suggest that AQP4 may be involved in forming edema in the inflammatory lesions of EAE accompanying with up-regulation of reactive astrocyte.
► We investigated expression of AQP4 in the spinal cord of rats immunized with MBP. ► AQO4 was histologically down-regulated in inflammatory microvessels of rats with EAE. ► Protein levels and mRNA of AQP4 were significantly decreased at the severe stage. ► Expression of GFAP-protein was significantly increased after stage of severe EAE. ► AQP4 may be involved in forming edema in the inflammatory lesions of EAE.
