Kolodney Goren, Dumin Elena, Safory Hazem, Rosenberg Dina, Mori Hisashi, Radzishevsky Inna, Wolosker Herman
From the Department of Biochemistry, Rappaport Faculty of Medicine and Research Institute, Technion-Israel Institute of Technology and.
the Laboratory of Clinical Biochemistry, Metabolic Unit, Rambam Health Care Campus, Haifa 31096, Israel, and.
J Biol Chem. 2015 Dec 25;290(52):31037-50. doi: 10.1074/jbc.M115.699496. Epub 2015 Nov 9.
D-Serine is a physiological co-agonist that activates N-methyl D-aspartate receptors (NMDARs) and is essential for neurotransmission, synaptic plasticity, and behavior. D-Serine may also trigger NMDAR-mediated neurotoxicity, and its dysregulation may play a role in neurodegeneration. D-Serine is synthesized by the enzyme serine racemase (SR), which directly converts L-serine to D-serine. However, many aspects concerning the regulation of D-serine production under physiological and pathological conditions remain to be elucidated. Here, we investigate possible mechanisms regulating the synthesis of D-serine by SR in paradigms relevant to neurotoxicity. We report that SR undergoes nucleocytoplasmic shuttling and that this process is dysregulated by several insults leading to neuronal death, typically by apoptotic stimuli. Cell death induction promotes nuclear accumulation of SR, in parallel with the nuclear translocation of GAPDH and Siah proteins at an early stage of the cell death process. Mutations in putative SR nuclear export signals (NESs) elicit SR nuclear accumulation and its depletion from the cytosol. Following apoptotic insult, SR associates with nuclear GAPDH along with other nuclear components, and this is accompanied by complete inactivation of the enzyme. As a result, extracellular D-serine concentration is reduced, even though extracellular glutamate concentration increases severalfold. Our observations imply that nuclear translocation of SR provides a fail-safe mechanism to prevent or limit secondary NMDAR-mediated toxicity in nearby synapses.
D-丝氨酸是一种生理性共激动剂,可激活N-甲基-D-天冬氨酸受体(NMDARs),对神经传递、突触可塑性和行为至关重要。D-丝氨酸也可能引发NMDAR介导的神经毒性,其失调可能在神经退行性变中起作用。D-丝氨酸由丝氨酸消旋酶(SR)合成,该酶直接将L-丝氨酸转化为D-丝氨酸。然而,在生理和病理条件下,关于D-丝氨酸产生的调控的许多方面仍有待阐明。在这里,我们在与神经毒性相关的范式中研究调节SR合成D-丝氨酸的可能机制。我们报告SR经历核质穿梭,并且这个过程被几种导致神经元死亡的损伤所失调,通常是由凋亡刺激引起的。细胞死亡诱导促进SR的核积累,与细胞死亡过程早期GAPDH和Siah蛋白的核转位同时发生。推测的SR核输出信号(NESs)中的突变引发SR的核积累及其从细胞质中的耗竭。在凋亡损伤后,SR与核GAPDH以及其他核成分结合,并且这伴随着该酶的完全失活。结果,细胞外D-丝氨酸浓度降低,尽管细胞外谷氨酸浓度增加了几倍。我们的观察结果表明,SR的核转位提供了一种故障安全机制,以防止或限制附近突触中继发性NMDAR介导的毒性。