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Contribution of Kv channel subunits to glutamate‐induced apoptosis in cultured rat hippocampal neurons
Author(s) -
Shen QiJun,
Zhao YuMing,
Cao DongXu,
Wang XiaoLiang
Publication year - 2009
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.22136
Subject(s) - hippocampal formation , neuroscience , glutamate receptor , apoptosis , chemistry , microbiology and biotechnology , biology , biophysics , biochemistry , receptor
Potassium channel dysfunction has been implicated in apoptosis in many pathological conditions. However, which Kv channel subunit is involved in glutamate‐induced apoptosis remains unknown. In this study, the contributions of nine Kvα and three Kvβ subunits to glutamate‐induced hippocampal neuronal apoptosis were investigated. Results showed that neuronal apoptosis was not obvious with 12 hr incubation of glutamate but increased markedly after 18 hr, which was attenuated by the Kv channel blocker TEA. Among all the Kv subunits investigated, gene and protein expression of Kv2.1 increased significantly before the appearance of neuronal apoptosis, whereas the Kv1.1 mRNA level decreased quickly, and protein expression was reduced gradually after the insult. Seven other Kvα subunits and three Kvβ subunits were not obviously affected over time. In addition, Kv1.1 overexpression could reduce glutamate‐induced hippocampal neuronal apoptosis. Therefore, the alterations of Kv1.1 and Kv2.1 might contribute to glutamate‐induced toxicity in hippocampal neurons. These findings suggest that these two Kv channel subunits may represent potential therapeutic targets for neuropathological conditions in which glutamate‐induced toxicity is thought to contribute to neuronal dysfunction. © 2009 Wiley‐Liss, Inc.