A Vesicular Transporter That Mediates Aspartate and Glutamate Neurotransmission
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作者:
Miyaji, Takaaki
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Okayama Univ, Adv Sci Res Ctr, Dept Genom & Prote, Kita Ku, Okayama 7008530, JapanOkayama Univ, Adv Sci Res Ctr, Dept Genom & Prote, Kita Ku, Okayama 7008530, Japan
Miyaji, Takaaki
[1
]
Omote, Hiroshi
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Okayama Univ, Dept Membrane Biochem, Grad Sch Med Dent & Pharmaceut Sci, Kita Ku, Okayama 7008530, JapanOkayama Univ, Adv Sci Res Ctr, Dept Genom & Prote, Kita Ku, Okayama 7008530, Japan
Omote, Hiroshi
[2
]
Moriyama, Yoshinori
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Okayama Univ, Adv Sci Res Ctr, Dept Genom & Prote, Kita Ku, Okayama 7008530, Japan
Okayama Univ, Dept Membrane Biochem, Grad Sch Med Dent & Pharmaceut Sci, Kita Ku, Okayama 7008530, JapanOkayama Univ, Adv Sci Res Ctr, Dept Genom & Prote, Kita Ku, Okayama 7008530, Japan
Moriyama, Yoshinori
[1
,2
]
机构:
[1] Okayama Univ, Adv Sci Res Ctr, Dept Genom & Prote, Kita Ku, Okayama 7008530, Japan
[2] Okayama Univ, Dept Membrane Biochem, Grad Sch Med Dent & Pharmaceut Sci, Kita Ku, Okayama 7008530, Japan
Aspartate, an excitatory amino acid, is known to be stored in synaptic vesicles and exocytosed from some neurons to perform aspartergic neurotransmission. Through in vitro reconstitution, we found that sialin, a lysosomal sialic acid exporter, is responsible for the vesicular storage of aspartate in hippocampal neurons and pinealocytes. Mutations found in Salla disease cause decreased aspartate transport activity without affecting sialic acid transport. Thus, sialin is a multifunctional transporter. It is possible that people with Salla disease lose the ability of aspartergic neurotransmission, and this could explain why Salla disease involves severe neurological defects.