Journal
NEUROCHEMISTRY INTERNATIONAL
Volume 55, Issue 4, Pages 219-225Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuint.2009.03.003
Keywords
NAA; Aspartate-N-acetyltransferase; Aspartate aminotransferase; Aminooxyacetic acid; Mitochondria; Cytoplasm; Microsomes
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Funding
- USUHS [C070PB, R070WG]
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N-acetylaspartate (NAA) is synthesized predominantly in neurons, and brain homogenate subfractionation studies suggest that biosynthesis occurs at both microsomal (cytoplasmic) and mitochondrial sites. We investigated NAA synthesis in SH-SY5Y human neuroblastoma cells using distinct metabolic precursors that are preferentially metabolized in mitochondria and cytoplasm. Incorporation of C-14-aspartate and C-14-malate into NAA was examined in the presence and absence of an inhibitor (aminooxyacetic acid, AOAA) of aspartate aminotransferase (AAT), a central enzyme involved in the biosynthesis of aspartate in mitochondria, and degradation of aspartate in the cytoplasm. AOAA increased the incorporation of C-14-aspartate into NAA, reflecting direct aspartate -> NAA synthesis in an extramitochondrial location. As expected, AOAA decreased incorporation of C-14-malate into NAA, reflecting NAA synthesis in mitochondria via the malate -> oxaloacetate -> aspartate -> NAA pathway. When C-14-malate was used as substrate, the C-14-NAA/C-14-aspartate ratio was over 20-fold higher than the ratio obtained with C-14-aspartate. Because NAA can only be synthesized from aspartate, the higher C-14-NAA/C-14-aspartate (product/substrate) ratio obtained with C-14-malate suggests greater NAA biosynthetic activity. We conclude that NAA biosynthesis occurs in both the cytoplasm and mitochondria of SH-SY5Y cells, and that the contribution from the mitochondrial compartment is quantitatively larger than that in the extramitochondrial compartment. Published by Elsevier Ltd.
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