首页> 美国卫生研究院文献>Frontiers in Molecular Neuroscience >Controversial Effects of D-Amino Acid Oxidase Activator (DAOA)/G72 on D-Amino Acid Oxidase (DAO) Activity in Human Neuronal Astrocyte and Kidney Cell Lines: The N-methyl D-aspartate (NMDA) Receptor Hypofunction Point of View
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Controversial Effects of D-Amino Acid Oxidase Activator (DAOA)/G72 on D-Amino Acid Oxidase (DAO) Activity in Human Neuronal Astrocyte and Kidney Cell Lines: The N-methyl D-aspartate (NMDA) Receptor Hypofunction Point of View

机译:D-氨基酸氧化酶激活剂(DAOA)/ G72对人神经元星形胶质细胞和肾脏细胞系中D-氨基酸氧化酶(DAO)活性的争议作用:N-甲基D-天冬氨酸(NMDA)受体功能低下的观点

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摘要

Dysfunction of D-amino acid oxidase (DAO) and DAO activator (DAOA)/G72 genes have been linked to neuropsychiatric disorders. The glutamate hypothesis of schizophrenia has proposed that increased DAO activity leads to decreased D-serine, which subsequently may lead to N-methyl-D-aspartate (NMDA) receptor hypofunction. It has been shown that DAOA binds to DAO and increases its activity. However, there are also studies showing DAOA decreases DAO activity. Thus, the effect of DAOA on DAO is controversial. We aimed to understand the effect of DAOA on DAO activity in neuron-like (SH-SY5Y), astrocyte-like (1321N1) and kidney-like (HEK293) human cell lines. DAO activity was measured based on the release of hydrogen peroxide and its interaction with Amplex Red reagent. We found that DAOA increases DAO activity only in HEK293 cells, but has no effect on DAO activity in SH-SY5Y and 1321N1 cells. This might be because of different signaling pathways, or due to lower DAO and DAOA expression in SH-SY5Y and 1321N1 cells compared to HEK293 cells, but also due to different compartmentalization of the proteins. The lower DAO and DAOA expression in neuron-like SH-SY5Y and astrocyte-like 1321N1 cells might be due to tightly regulated expression, as previously reported in the human post-mortem brain. Our simulation experiments to demonstrate the interaction between DAOA and human DAO (hDAO) showed that hDAO holoenzyme [hDAO with flavine adenine dinucleotide (FAD)] becomes more flexible and misfolded in the presence of DAOA, whereas DAOA had no effect on hDAO apoprotein (hDAO without FAD), which indicate that DAOA inactivates hDAO holoenzyme. Furthermore, patch-clamp analysis demonstrated no effect of DAOA on NMDA receptor activity in NR1/NR2A HEK293 cells. In summary, the interaction between DAO and DAOA seems to be cell type and its biochemical characteristics dependent which still needs to be elucidated.
机译:D-氨基酸氧化酶(DAO)和DAO激活剂(DAOA)/ G72基因的功能障碍与神经精神疾病有关。精神分裂症的谷氨酸假说已经提出,增加的DAO活性导致减少的D-丝氨酸,其随后可能导致N-甲基-D-天冬氨酸(NMDA)受体功能减退。已经显示DAOA与DAO结合并增加其活性。但是,也有研究表明DAOA会降低DAO活性。因此,DAOA对DAO的作用是有争议的。我们旨在了解DAOA对神经元样(SH-SY5Y),星形胶质样(1321N1)和肾样(HEK293)人细胞系中DAO活性的影响。基于过氧化氢的释放及其与Amplex Red试剂的相互作用来测量DAO活性。我们发现DAOA仅在HEK293细胞中增加DAO活性,但对SH-SY5Y和1321N1细胞中的DAO活性没有影响。这可能是由于不同的信号传导途径,或由于与HEK293细胞相比,SH-SY5Y和1321N1细胞中的DAO和DAOA表达降低,也可能是由于蛋白质的区室化不同。如先前在人类尸体大脑中报道的那样,神经元样SH-SY5Y和星形胶质样1321N1细胞中DAO和DAOA的较低表达可能是由于表达调控严格。我们的模拟实验证明了DAOA与人DAO(hDAO)之间的相互作用,结果表明,在DAOA存在下,hDAO全酶[hDAO与黄连腺嘌呤二核苷酸(FAD)]变得更灵活且折叠错误,而DAOA对hDAO载脂蛋白(hDAO)没有影响没有FAD),这表明DAOA可以使hDAO全酶失活。此外,膜片钳分析表明DAOA对NR1 / NR2A HEK293细胞的NMDA受体活性没有影响。总之,DAO和DAOA之间的相互作用似乎是细胞类型及其依赖于其生化特性的,尚需阐明。

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