Cellular distribution of the neutral amino acid transporter subtype ASCT2 in mouse brain

被引:58
|
作者
Gliddon, Catherine M.
Shao, Zongjun
LeMaistre, Jillian L.
Anderson, Christopher M. [1 ]
机构
[1] St Boniface Hosp Res Ctr, Div Neurodegenerat Disorders, Winnipeg, MB R2H 2A6, Canada
基金
加拿大健康研究院;
关键词
ASCT2; d-serine transport; glutamine transport; l-serine transport; astrocyte; immunohistochemistry; HIGH-AFFINITY UPTAKE; D-SERINE; RAT-BRAIN; GLUTAMINE EFFLUX; PRIMARY CULTURE; NMDA RECEPTORS; GLYCINE SITE; ASTROCYTES; NEURONS; PROTEIN;
D O I
10.1111/j.1471-4159.2008.05767.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ASCT2 is an ASC (alanine-, serine-, cysteine-preferring) neutral amino acid exchanger that may regulate CNS function by transporting amino acid substrates including l-serine, l-cysteine, l-glutamine, l-glutamate and d-serine. Despite the potentially important role of ASCT2 in influencing metabolic and signaling functions of these amino acids in brain, there has been little description of its distribution in brain tissue. We employed a commercially available human ASCT2 antibody in immunohistochemistry studies in adult mouse brain and found a wide regional distribution for ASCT2 that was limited to dendrites labeled by anti-microtubule-associated protein-2 in cortex, hippocampus and striatum. No ASCT2 immunoreactivity was observed in areas labeled by antibodies against a neuronal cell body marker (NeuN), or either of the astrocyte markers, glial fibrillary acidic protein or S100 beta. In cerebellum both Purkinje cell bodies and dendrites were positive for ASCT2 immunoreactivity. In support of a dendritic localization for ASCT2 in cortex, low affinity (K-T > 1 mM), Na+-dependent d-serine and l-glutamine uptake characteristic of ASCT2-mediated transport was observed in P2 synaptosomal preparations. These results suggest that ASCT2 may be an important neuronal neutral amino acid transporter and highlight a discrepancy between findings of astrocyte ASCT2 function in tissue culture and brain in situ.
引用
收藏
页码:372 / 383
页数:12
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