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神经精神疾病中富含纹状体的蛋白酪氨酸磷酸酶(STEP)功能的破坏。

Disruption of striatal-enriched protein tyrosine phosphatase (STEP) function in neuropsychiatric disorders.

作者信息

Karasawa Takatoshi, Lombroso Paul J

机构信息

Department of Molecular Neurobiology, Institute for Developmental Research, Aichi Human Service Center, Kasugai, Aichi 480-0392, Japan.

Departments of Neurobiology, Psychiatry and Child Study Center, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

Neurosci Res. 2014 Dec;89:1-9. doi: 10.1016/j.neures.2014.08.018. Epub 2014 Sep 10.

DOI:10.1016/j.neures.2014.08.018
PMID:25218562
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4259835/
Abstract

Striatal-enriched protein tyrosine phosphatase (STEP) is a brain-specific tyrosine phosphatase that plays a major role in the development of synaptic plasticity. Recent findings have implicated STEP in several psychiatric and neurological disorders, including Alzheimer's disease, schizophrenia, fragile X syndrome, Huntington's disease, stroke/ischemia, and stress-related psychiatric disorders. In these disorders, STEP protein expression levels and activity are dysregulated, contributing to the cognitive deficits that are present. In this review, we focus on the most recent findings on STEP, discuss how STEP expression and activity are maintained during normal cognitive function, and how disruptions in STEP activity contribute to a number of illnesses.

摘要

富含纹状体蛋白酪氨酸磷酸酶(STEP)是一种大脑特异性酪氨酸磷酸酶,在突触可塑性的发展中起主要作用。最近的研究结果表明,STEP与多种精神和神经疾病有关,包括阿尔茨海默病、精神分裂症、脆性X综合征、亨廷顿舞蹈症、中风/缺血以及与应激相关的精神疾病。在这些疾病中,STEP蛋白表达水平和活性失调,导致了所出现的认知缺陷。在本综述中,我们重点关注STEP的最新研究结果,讨论在正常认知功能期间STEP的表达和活性是如何维持的,以及STEP活性的破坏如何导致多种疾病。

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本文引用的文献

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Inhibitor of the tyrosine phosphatase STEP reverses cognitive deficits in a mouse model of Alzheimer's disease.酪氨酸磷酸酶STEP抑制剂可逆转阿尔茨海默病小鼠模型中的认知缺陷。
PLoS Biol. 2014 Aug 5;12(8):e1001923. doi: 10.1371/journal.pbio.1001923. eCollection 2014 Aug.
2
cAMP-PKA phosphorylation of tau confers risk for degeneration in aging association cortex.cAMP-PKA 对 tau 的磷酸化使衰老相关皮质中的退行性病变风险增加。
Proc Natl Acad Sci U S A. 2014 Apr 1;111(13):5036-41. doi: 10.1073/pnas.1322360111. Epub 2014 Mar 18.
3
Inhibition of striatal-enriched tyrosine phosphatase 61 in the dorsomedial striatum is sufficient to increased ethanol consumption.抑制背侧纹状体中富含丝氨酸的酪氨酸磷酸酶 61 足以增加乙醇的摄入量。
J Neurochem. 2014 Jun;129(6):1024-34. doi: 10.1111/jnc.12701. Epub 2014 Mar 27.
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Neuroprotective role of a brain-enriched tyrosine phosphatase, STEP, in focal cerebral ischemia.脑丰富型酪氨酸磷酸酶 STEP 在局灶性脑缺血中的神经保护作用。
J Neurosci. 2013 Nov 6;33(45):17814-26. doi: 10.1523/JNEUROSCI.2346-12.2013.
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Tyrosine phosphatase STEP61 negatively regulates amyloid β-mediated ERK/CREB signaling pathways via α7 nicotinic acetylcholine receptors.酪氨酸磷酸酶 STEP61 通过α7 型烟碱型乙酰胆碱受体负调控淀粉样β介导的 ERK/CREB 信号通路。
J Neurosci Res. 2013 Dec;91(12):1581-90. doi: 10.1002/jnr.23263. Epub 2013 Oct 3.
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