Abstract
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.
Original language | English |
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Pages (from-to) | 1783-1785 |
Number of pages | 3 |
Journal | Biological and Pharmaceutical Bulletin |
Volume | 33 |
Issue number | 11 |
DOIs | |
Publication status | Published - 2010 |
Keywords
- Aspartate
- Neurotransmission
- Salla disease
- Veicular glutamate transporter
- Vesicular excitatory amino acid transporter
ASJC Scopus subject areas
- Pharmacology
- Pharmaceutical Science