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本文引用的文献

1
High expression of antizyme inhibitor 2, an activator of ornithine decarboxylase in steroidogenic cells of human gonads.高表达抗酶抑制剂 2,一种在人性腺类固醇生成细胞中鸟氨酸脱羧酶的激活剂。
Histochem Cell Biol. 2009 Dec;132(6):633-8. doi: 10.1007/s00418-009-0636-7. Epub 2009 Sep 16.
2
Expression of antizyme inhibitor 2 in mast cells and role of polyamines as selective regulators of serotonin secretion.肥大细胞中抗酶抑制剂 2 的表达及多胺作为选择性调控 5-羟色胺分泌的作用。
PLoS One. 2009 Aug 31;4(8):e6858. doi: 10.1371/journal.pone.0006858.
3
Ornithine decarboxylase regulates the activity and localization of rhoA via polyamination.鸟氨酸脱羧酶通过多胺化作用调节RhoA的活性和定位。
Exp Cell Res. 2009 Apr 1;315(6):1008-14. doi: 10.1016/j.yexcr.2009.01.029. Epub 2009 Feb 11.
4
Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.131例伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)患者中NOTCH3突变与嗜刚果红物质(GOM)的一致性。
Brain. 2009 Apr;132(Pt 4):933-9. doi: 10.1093/brain/awn364. Epub 2009 Jan 27.
5
Spermine binding to Parkinson's protein alpha-synuclein and its disease-related A30P and A53T mutants.精胺与帕金森病蛋白α-突触核蛋白及其疾病相关的A30P和A53T突变体的结合。
J Phys Chem B. 2008 Sep 4;112(35):11147-54. doi: 10.1021/jp801175w. Epub 2008 Aug 9.
6
Antizyme inhibitor 2 (AZIN2/ODCp) stimulates polyamine uptake in mammalian cells.抗酶抑制剂2(AZIN2/ODCp)刺激哺乳动物细胞摄取多胺。
J Biol Chem. 2008 Jul 25;283(30):20761-9. doi: 10.1074/jbc.M801024200. Epub 2008 May 28.
7
Rab GTPases and their roles in brain neurons and glia.Rab 小 GTP 酶及其在脑神经元和神经胶质细胞中的作用。
Brain Res Rev. 2008 Jun;58(1):236-46. doi: 10.1016/j.brainresrev.2008.04.006. Epub 2008 Apr 12.
8
ODCp, a brain- and testis-specific ornithine decarboxylase paralogue, functions as an antizyme inhibitor, although less efficiently than AzI1.ODCp是一种在大脑和睾丸中特异表达的鸟氨酸脱羧酶旁系同源物,作为一种抗酶抑制剂发挥作用,尽管其效率低于AzI1。
Biochem J. 2008 Mar 15;410(3):613-9. doi: 10.1042/BJ20071423.
9
Human ornithine decarboxylase paralogue (ODCp) is an antizyme inhibitor but not an arginine decarboxylase.人类鸟氨酸脱羧酶旁系同源物(ODCp)是一种抗酶抑制剂,但不是精氨酸脱羧酶。
Biochem J. 2008 Jan 1;409(1):187-92. doi: 10.1042/BJ20071004.
10
Abeta oligomers induce neuronal oxidative stress through an N-methyl-D-aspartate receptor-dependent mechanism that is blocked by the Alzheimer drug memantine.β淀粉样蛋白寡聚体通过一种N-甲基-D-天冬氨酸受体依赖性机制诱导神经元氧化应激,而阿尔茨海默病药物美金刚可阻断该机制。
J Biol Chem. 2007 Apr 13;282(15):11590-601. doi: 10.1074/jbc.M607483200. Epub 2007 Feb 16.

脑神经元表达鸟氨酸脱羧酶激活酶抑制剂 2 并在阿尔茨海默病中积累。

Brain neurons express ornithine decarboxylase-activating antizyme inhibitor 2 with accumulation in Alzheimer's disease.

机构信息

Department of Pathology, Haartman Institute, University of Helsinki, Helsinki, Finland.

出版信息

Brain Pathol. 2010 May;20(3):571-80. doi: 10.1111/j.1750-3639.2009.00334.x. Epub 2009 Sep 22.

DOI:10.1111/j.1750-3639.2009.00334.x
PMID:19832840
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8094758/
Abstract

Polyamines are small cationic molecules that in adult brain are connected to neuronal signaling by regulating inward-rectifier K(+)-channels and different glutamate receptors. Antizyme inhibitors (AZINs) regulate the cellular uptake of polyamines and activate ornithine decarboxylase (ODC), the rate-limiting enzyme of polyamine synthesis. Elevated levels of ODC activity and polyamines are detected in various brain disorders including stroke and Alzheimer's disease (AD). We originally reported a novel brain- and testis-specific AZIN, called AZIN2, the distribution of which we have now studied in normal and diseased human brain by in situ hybridization and immunohistochemistry. We found the highest accumulation of AZIN2 in a pearl-on-the-string-like distribution along the axons in both the white and gray matter. AZIN2 was also detected in a vesicle-like distribution in the somas of selected cortical pyramidal neurons. Double-immunofluorescence staining revealed co-localization of AZIN2 and N-methyl D-aspartate-type glutamate receptors (NMDARs) in pyramidal neurons of the cortex. Moreover, we found accumulation of AZIN2 in brains affected by AD, but not by other neurodegenerative disorders (CADASIL or Lewy body disease). ODC activity is mostly linked to cell proliferation, whereas its regulation by AZIN2 in post-mitotically differentiated neurons of the brain apparently serves different purposes. The subcellular distribution of AZIN2 suggests a role in vesicular trafficking.

摘要

多胺是小分子阳离子,在成年大脑中通过调节内向整流钾 (K+) 通道和不同的谷氨酸受体与神经元信号有关。抗酶抑制剂 (AZINs) 调节多胺的细胞摄取并激活鸟氨酸脱羧酶 (ODC),这是多胺合成的限速酶。在各种脑疾病中,包括中风和阿尔茨海默病 (AD),都检测到 ODC 活性和多胺水平升高。我们最初报道了一种新型的脑和睾丸特异性 AZIN,称为 AZIN2,我们现在通过原位杂交和免疫组织化学研究了其在正常和患病人脑中的分布。我们发现 AZIN2 在白质和灰质中的轴突上呈串珠样分布,积累量最高。AZIN2 也以囊泡样分布存在于选定的皮质锥体细胞的胞体中。双重免疫荧光染色显示 AZIN2 和 N-甲基 D-天冬氨酸型谷氨酸受体 (NMDAR) 在皮质锥体细胞中存在共定位。此外,我们发现 AZIN2 在受 AD 影响的大脑中积累,但不受其他神经退行性疾病 (CADASIL 或路易体病) 的影响。ODC 活性主要与细胞增殖有关,而其在脑内有丝分裂后分化神经元中的 AZIN2 调节显然有不同的作用。AZIN2 的亚细胞分布表明其在囊泡运输中具有作用。