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Expression of annexin A2 in GABAergic interneurons in the normal rat brain
Author(s) -
Zhao WeiQin,
Lu Bai
Publication year - 2007
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2006.04311.x
Subject(s) - gabaergic , biology , neuroscience , microbiology and biotechnology , parvalbumin , depolarization , glutamate decarboxylase , neurodegeneration , glutamate receptor , extracellular , excitotoxicity , synaptophysin , in situ hybridization , neuron , chemistry , biochemistry , messenger rna , immunohistochemistry , medicine , biophysics , inhibitory postsynaptic potential , receptor , enzyme , immunology , gene , disease
Expression of the Ca 2+ ‐dependent phospholipids binding protein annexin A2 (ANX2) in the brain is thought to be largely associated with brain pathological conditions such as tumor, inflammation, and neurodegeneration. The recent findings that ANX2 heterotetramer is involved in learning and neuronal activities necessitates a systematic investigation of the physiological expression of ANX2 in the brain. With combination of in situ hybridization and immunohistochemistry, ANX2 mRNA and protein were specifically detected in a group of GABAergic interneurons throughout the brain. Although ANX2 was absent from the interior of pyramidal neurons, it was found on the membrane and seemly the extracellular space of those neurons, where they closely co‐localized with glutamate decarboxylase terminals. In cultured developing neurons, ANX2 was present at high concentrations in the growth cones co‐distributing with several growth‐associated proteins such as growth associated protein 43 (GAP43), turned on after division/Ulip/CRMP (TUC‐4), tubulin, and tissue‐plasminogen activator. It then became predominantly distributed on the membrane and mostly in axonal branches as neurons grew and extended synaptic networks. ANX2 was also secreted from cultured neurons, in a membrane‐bound form that was Ca 2+ ‐dependent, which was significantly increased by neuronal depolarization. These results may have implications in the function and regulatory mechanism of ANX2 in the normal brain.