The mitochondrial aspartate/glutamate carrier isoform 1 gene expression is regulated by CREB in neuronal cells

被引:19
作者
Menga, Alessio [1 ]
Iacobazzi, Vito [1 ]
Infantino, Vittoria [2 ]
Avantaggiati, Maria Laura [3 ]
Palmieri, Ferdinando [1 ]
机构
[1] Univ Bari, Dept Biosci Biotechnol & Biopharmaceut, I-70125 Bari, Italy
[2] Univ Basilicata, Dept Sci, I-85100 Potenza, Italy
[3] Georgetown Univ, Dept Oncol, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
关键词
Aspartate/glutamate carrier; CREB; Ca2+; MYELIN LIPID-SYNTHESIS; TRANSPORTER FAMILY SLC25; ELEMENT-BINDING PROTEIN; ACETYL-L-ASPARTATE; N-ACETYLASPARTATE; DOWN-REGULATION; SUBCELLULAR-LOCALIZATION; TRANSCRIPTION FACTOR; ALZHEIMERS-DISEASE; OXIDATIVE STRESS;
D O I
10.1016/j.biocel.2015.01.004
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
The aspartate/glutamate carrier isoform 1 is an essential mitochondrial transporter that exchanges intramitochondrial aspartate and cytosolic glutamate across the inner mitochondrial membrane. It is expressed in brain, heart and muscle and is involved in important biological processes, including myelination. However, the signals that regulate the expression of this transporter are still largely unknown. In this study we first identify a CREB binding site within the aspartate/glutamate carrier gene promoter that acts as a strong enhancer element in neuronal SH-SY5Y cells. This element is regulated by active, phosphorylated CREB protein and by signal pathways that modify the activity of CREB itself and, most noticeably, by intracellular Ca2+ levels. Specifically, aspartate/glutamate carrier gene expression is induced via CREB by forskolin while it is inhibited by the PICA inhibitor, H89. Furthermore, the CREB-induced activation of gene expression is increased by thapsigargin, which enhances cytosolic Ca2+, while it is inhibited by BAPTA-AM that reduces cytosolic Ca2+ or by STO-609, which inhibits CaMK-IV phosphorylation. We further show that CREB-dependent regulation of aspartate/glutamate carrier gene expression occurs in neuronal cells in response to pathological (inflammation) and physiological (differentiation) conditions. Since this carrier is necessary for neuronal functions and is involved in myelinogenesis, our results highlight that targeting of CREB activity and Ca2+ might be therapeutically exploited to increase aspartate/glutamate carrier gene expression in neurodegenerative diseases. (C) 2015 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:157 / 166
页数:10
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