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Neuronal glutamate transporter EAAT4 is expressed in astrocytes
Author(s) -
Hu WenHui,
Walters Winston M.,
Xia XiaoMei,
Karmally Shaffiat A.,
Bethea John R.
Publication year - 2003
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.10268
Subject(s) - astrocyte , biology , glutamatergic , glial fibrillary acidic protein , glutamate receptor , excitotoxicity , neuroglia , microbiology and biotechnology , forebrain , neuroscience , biochemistry , central nervous system , immunohistochemistry , receptor , immunology
Abstract High‐affinity excitatory amino acid transporters (EAATs) are essential to terminate glutamatergic neurotransmission and to prevent excitotoxicity. To date, five distinct EAATs have been cloned from animal and human tissues: GLAST (EAAT1), GLT‐1 (EAAT2), EAAC1 (EAAT3), EAAT4, and EAAT5. EAAT1 and EAAT2 are commonly known as glial glutamate transporters, whereas EAAT3, EAAT4, and EAAT5 are neuronal. EAAT4 is largely expressed in cerebellar Purkinje cells. In this study, using immunohistochemistry and Western blotting, we found that EAAT4‐like immunoreactivity (ir) is enriched in the spinal cord and forebrain. Double‐labeled fluorescent immunostaining and confocal image analysis indicated that EAAT4‐like ir colocalizes with an astrocytic marker, glial fibrillary acidic protein (GFAP). The astrocytic localization of EAAT4 was further confirmed in astrocyte cultures by double‐labeled fluorescent immunocytochemistry and Western blotting. Reverse transcriptase‐polymerase chain reaction analysis demonstrated mRNA expression of EAAT4 in astrocyte cultures. Sequencing confirmed the specificity of the amplified fragment. These results demonstrate that EAAT4 is expressed in astrocytes. This astrocytic localization of neuronal EAAT4 may reveal a new function of EAAT4 in the central nervous system. © 2003 Wiley‐Liss, Inc.