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2
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Wild-type huntingtin ameliorates striatal neuronal atrophy but does not prevent other abnormalities in the YAC128 mouse model of Huntington disease.野生型亨廷顿蛋白可改善纹状体神经元萎缩,但不能预防亨廷顿病YAC128小鼠模型中的其他异常。
BMC Neurosci. 2006 Dec 5;7:80. doi: 10.1186/1471-2202-7-80.
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Differential susceptibility to excitotoxic stress in YAC128 mouse models of Huntington disease between initiation and progression of disease.亨廷顿舞蹈病YAC128小鼠模型在疾病起始和进展阶段对兴奋性毒性应激的易感性差异。
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本文引用的文献

1
Early increase in extrasynaptic NMDA receptor signaling and expression contributes to phenotype onset in Huntington's disease mice.早期 extrasynaptic NMDA 受体信号和表达的增加导致亨廷顿病小鼠表型的出现。
Neuron. 2010 Jan 28;65(2):178-90. doi: 10.1016/j.neuron.2010.01.008.
2
Serines 13 and 16 are critical determinants of full-length human mutant huntingtin induced disease pathogenesis in HD mice.丝氨酸 13 和 16 是全长人类突变 huntingtin 在 HD 小鼠中诱导疾病发病机制的关键决定因素。
Neuron. 2009 Dec 24;64(6):828-40. doi: 10.1016/j.neuron.2009.11.020.
3
Genetic and pharmacological inhibition of calcineurin corrects the BDNF transport defect in Huntington's disease.基因和药物抑制钙调神经磷酸酶可纠正亨廷顿病中 BDNF 的转运缺陷。
Mol Brain. 2009 Oct 27;2:33. doi: 10.1186/1756-6606-2-33.
4
Reduced calcineurin protein levels and activity in exon-1 mouse models of Huntington's disease: role in excitotoxicity.亨廷顿病外显子 1 小鼠模型中钙调神经磷酸酶蛋白水平和活性降低:在兴奋性毒性中的作用。
Neurobiol Dis. 2009 Dec;36(3):461-9. doi: 10.1016/j.nbd.2009.08.012. Epub 2009 Sep 4.
5
Mouse models of Huntington disease: variations on a theme.亨廷顿病的小鼠模型:同一主题的变体
Dis Model Mech. 2009 Mar-Apr;2(3-4):123-9. doi: 10.1242/dmm.002451.
6
Differential susceptibility to excitotoxic stress in YAC128 mouse models of Huntington disease between initiation and progression of disease.亨廷顿舞蹈病YAC128小鼠模型在疾病起始和进展阶段对兴奋性毒性应激的易感性差异。
J Neurosci. 2009 Feb 18;29(7):2193-204. doi: 10.1523/JNEUROSCI.5473-08.2009.
7
Phosphorylation of huntingtin reduces the accumulation of its nuclear fragments.亨廷顿蛋白的磷酸化减少了其核碎片的积累。
Mol Cell Neurosci. 2009 Feb;40(2):121-7. doi: 10.1016/j.mcn.2008.09.007. Epub 2008 Oct 18.
8
Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neurons.亨廷顿蛋白磷酸化作为神经元中顺行/逆行运输的分子开关。
EMBO J. 2008 Aug 6;27(15):2124-34. doi: 10.1038/emboj.2008.133. Epub 2008 Jul 10.
9
Activation of brain protein phosphatase-1(I) following cardiac arrest and resuscitation involving an interaction with 14-3-3 gamma.心脏骤停与复苏后涉及与14-3-3γ相互作用的脑蛋白磷酸酶-1(I)的激活
J Neurochem. 2008 Jun;105(5):2029-38. doi: 10.1111/j.1471-4159.2008.05300.x. Epub 2008 Feb 14.
10
Calcineurin is involved in the early activation of NMDA-mediated cell death in mutant huntingtin knock-in striatal cells.钙调神经磷酸酶参与突变亨廷顿蛋白基因敲入纹状体细胞中NMDA介导的细胞死亡的早期激活过程。
J Neurochem. 2008 Jun;105(5):1596-612. doi: 10.1111/j.1471-4159.2008.05252.x. Epub 2008 Jan 24.

YAC128 神经元中海马汀丝氨酸 421 位点的磷酸化与 YAC128 神经元对 NMDA 介导的兴奋性毒性的保护有关,并且可被蛋白磷酸酶 1 和 2A 调节。

Phosphorylation of huntingtin at Ser421 in YAC128 neurons is associated with protection of YAC128 neurons from NMDA-mediated excitotoxicity and is modulated by PP1 and PP2A.

机构信息

Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia V5Z 4H4, Canada.

出版信息

J Neurosci. 2010 Oct 27;30(43):14318-29. doi: 10.1523/JNEUROSCI.1589-10.2010.

DOI:10.1523/JNEUROSCI.1589-10.2010
PMID:20980587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6634803/
Abstract

YAC transgenic mice expressing poly(Q)-expanded full-length huntingtin (mhtt) recapitulate many behavioral and neuropathological features of Huntington disease (HD). We have previously observed a reduction in phosphorylation of mhtt at S421 in the presence of the mutation for HD. In addition, phosphorylation of normal S421-htt is reduced after excitotoxic stimulation of NMDA receptors (NMDARs). To test whether NMDAR stimulation contributes to reduced pS421-htt levels in HD, we determined phosphorylation of htt at Ser421 after NMDA-induced excitotoxicity in neurons from YAC128 mice. Here, we report that the total level of pS421-htt is reduced in YAC128 primary neurons after excitotoxic NMDAR stimulation. Similarly, the total level of pS421-htt is reduced in YAC128 transgenic mice after quinolinic acid injection into the striatum. In contrast, loss of phosphorylation of pS421-htt is prevented in YAC mice that never develop clinical or neuropathological features of HD [the caspase 6-resistant YAC128 transgene (C6R)]. To gain insight into the mechanisms underlying these findings, we determined that the Ser/Thr protein phosphatases PP1 and PP2A dephosphorylate pS421-htt in situ and after excitotoxic stimulation of NMDARs in neurons. Furthermore, increasing the phosphorylation of htt at S421 by blocking PP1 and PP2A activity protects YAC128 striatal neurons from NMDA-induced cell death. These results, together with the observed modulation of pS421-htt levels by dopamine, the reduced expression of PP1 inhibitor Darpp-32 in the striatum of YAC128 mice, and the reduced phosphorylation of PP1 substrate CreB, point to altered regulation of phosphatase activity in HD and highlight enhancing phosphorylation of htt at S421 as a therapeutic target.

摘要

表达聚 Q 扩展全长亨廷顿蛋白 (mhtt) 的 YAC 转基因小鼠重现亨廷顿病 (HD) 的许多行为和神经病理学特征。我们之前观察到在 HD 突变存在的情况下,mhtt 在 S421 处的磷酸化减少。此外,NMDA 受体 (NMDAR) 兴奋毒性刺激后,正常 S421-htt 的磷酸化减少。为了测试 NMDAR 刺激是否导致 HD 中 pS421-htt 水平降低,我们在 YAC128 小鼠的神经元中测定了 NMDA 诱导兴奋毒性后 htt 在 S421 处的磷酸化。在这里,我们报告说,在兴奋毒性 NMDAR 刺激后,YAC128 原代神经元中 pS421-htt 的总水平降低。类似地,在 YAC128 转基因小鼠纹状体注射喹啉酸后,pS421-htt 的总水平降低。相比之下,在从未出现 HD 临床或神经病理学特征的 YAC 小鼠 (caspase 6 抗性 YAC128 转基因 (C6R)) 中,pS421-htt 的磷酸化丢失得到预防。为了深入了解这些发现的机制,我们确定丝氨酸/苏氨酸蛋白磷酸酶 PP1 和 PP2A 在原位和 NMDAR 兴奋毒性刺激后使 pS421-htt 去磷酸化。此外,通过阻断 PP1 和 PP2A 活性增加 htt 在 S421 处的磷酸化可保护 YAC128 纹状体神经元免受 NMDA 诱导的细胞死亡。这些结果,加上多巴胺对 pS421-htt 水平的调节,YAC128 小鼠纹状体中 PP1 抑制剂 Darpp-32 的表达降低,以及 PP1 底物 CreB 的磷酸化减少,表明 HD 中磷酸酶活性的调节发生改变,并强调增加 htt 在 S421 处的磷酸化作为治疗靶点。