Lysosomal amino acid transporter LYAAT‐1 in the rat central nervous system: An in situ hybridization and immunohistochemical study
- 16 May 2003
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 462 (1) , 71-89
- https://doi.org/10.1002/cne.10712
Abstract
A first mammalian lysosomal transporter (LYAAT‐1) was recently identified and functionally characterized. Preliminary immunocytochemical data revealed that LYAAT‐1 localizes to lysosomes in some neurons. In order to determine whether it is expressed in specific neuron populations and other cell types, and to confirm whether it is localized at the membrane of lysosomes, we used in situ hybridization and immunohistochemistry methods in adult rat central nervous system (CNS). We found that LYAAT‐1 is expressed in most areas of the CNS, specifically in neurons, but also in choroid plexus and ependymal epithelium cells. LYAAT‐1‐IR (immunoreactivity) levels varied among different neuroanatomical structures but were present in neurons independently of the neurotransmitter used (glutamate, GABA, acetylcholine, noradrenaline, serotonin, or glycine). Light and confocal microscopy demonstrated that LYAAT‐1 and the lysosomal marker cathepsin D colocalized throughout the brain and electron microscopy showed that LYAAT‐1‐IR was associated with lysosomal membranes. In addition, LYAAT‐1‐IR was also found associated with other membranes belonging to the Golgi apparatus and lateral saccules and less frequently with multivesicular bodies, endoplasmic reticulum, and occasionally with the plasma membrane. The localization of LYAAT‐1 at the lysosomal membrane is consistent with the view that it mediates amino acid efflux from lysosomes. Furthermore, its cell expression pattern suggests that it may contribute to specialized cellular function in the rat CNS such as neuronal metabolism, neurotransmission, and control of brain amino acid homeostasis. J. Comp. Neurol. 462:71–89, 2003.Keywords
Funding Information
- Hoechst Marion Roussel fellowship and funding
- European Economic Community fellowship
- Fondation pour la Recherche Médicale fellowship
- Inserm
- Association Française contre les Myopathies
- CNRS
This publication has 61 references indexed in Scilit:
- Functional Characterization of Two Novel Mammalian Electrogenic Proton-dependent Amino Acid CotransportersJournal of Biological Chemistry, 2002
- Localization of the Brain-Specific High-Affinityl-Proline Transporter in Cultured Hippocampal Neurons: Molecular Heterogeneity of Synaptic TerminalsMolecular and Cellular Neuroscience, 1999
- Immuno-Localization of H+/Peptide Cotransporter in Rat Digestive TractBiochemical and Biophysical Research Communications, 1996
- Comparative Analysis of 13C-Enriched Metabolites Released in the Medium of Cerebellar and Cortical Astrocytes Incubated with [1-13C]GlucoseEuropean Journal of Biochemistry, 1995
- Comparative Analysis of 13C-Enriched Metabolites Released in the Medium of Cerebellar and Cortical Astrocytes Incubated with [1-13C]GlucoseEuropean Journal of Biochemistry, 1995
- Uptake, release and metabolism of alaume in neurons and astrocytes in primary culturesJournal of Neuroscience Research, 1993
- Segregation of MHC class II molecules from MHC class I molecules in the Golgi complex for transport to lysosomal compartmentsNature, 1991
- Hyperprolinaemia type I and white matter disease: Coincidence or causal relationshipEuropean Journal of Pediatrics, 1989
- Sorting of mannose 6-phosphate receptors and lysosomal membrane proteins in endocytic vesicles.The Journal of cell biology, 1988
- Defective hydroxyproline metabolism in type II hyperprolinemiaBiochemical Medicine, 1974