Abstract
Glutamate is the major excitatory neurotransmitter in the mammalian CNS. It is loaded into synaptic vesicles by a proton gradient-dependent uptake system and is released by exocytosis upon stimulation. Recently, two mammalian isoforms of a vesicular glutamate transporter, VGLUT1 and VGLUT2, have been identified, the expression of which enables quantal release of glutamate from glutamatergic neurons. Here, we report a novel isoform of a human vesicular glutamate transporter (hVGLUT3). The predicted amino acid sequence of hVGLUT3 shows 72% identity to both hVGLUT1 and hVGLUT2. hVGLUT3 functions as a vesicular glutamate transporter with similar properties to the other isoforms when it is heterologously expressed in a neuroendocrine cell line. Although mammalian VGLUT1 and VGLUT2 exhibit a complementary expression pattern covering all glutamatergic pathways in the CNS, expression of hVGLUT3 overlaps with them in some brain areas, suggesting molecular diversity that may account for physiological heterogeneity in glutamatergic synapses.
MeSH Terms
Amino Acid Sequence
Amino Acid Transport Systems, Acidic/chemistry,genetics
Biological Transport
Blotting, Northern
Brain/metabolism
Cell Membrane/metabolism
Central Nervous System/metabolism
Cloning, Molecular
DNA, Complementary/metabolism
Glutamic Acid/metabolism
Humans
Molecular Sequence Data
Phylogeny
RNA, Messenger/metabolism
Sequence Homology, Amino Acid
Time Factors
Tissue Distribution
Transfection
Vesicular Glutamate Transport Proteins
Chemicals
Amino Acid Transport Systems, Acidic
DNA, Complementary
RNA, Messenger
SLC17A8 protein, human
Vesicular Glutamate Transport Proteins
Glutamic Acid
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Takamori Shigeo
Department of Neurobiology, Max-Planck Institute for Biophysical Chemistry, Göttingen, Germany.
Malherbe Pari
Broger Clemens
Jahn Reinhard
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