组蛋白去乙酰化酶6在阿尔茨海默病中的作用
被引量:4
摘要
组蛋白去乙酰化酶6(HDAC6)是HDAC家族中Ⅱb类成员之一,具有去乙酰化酶活性和参与细胞内异常蛋白降解的功能。近来研究发现HDAC6参与调节Tau蛋白磷酸化、糖原合成酶激酶3β(GSK3β)影响线粒体运输等有关的生化过程,提示HDAC6可能与AD的发生有关,是治疗AD的潜在靶点。本文论述了HDAC6的结构与功能、HDAC6的选择性抑制剂以及在AD中的作用。
出处
《国际神经病学神经外科学杂志》
2011年第4期348-352,共5页
Journal of International Neurology and Neurosurgery
基金
国家自然科学基金(81071007)
福建省自然科学杰出青年基金(2009J06015)
参考文献28
-
1Dhakal BK, Mulvey MA. Uropathogenic Escherichia coli in- vades host cells via an HDAC6-modulated microtubule-de- pendent pathway. J Biol Chem, 2009, 284 (1): 446- 454.
-
2Scroggins BT, Robzyk K, Wang D, et al. An acetylation site in the middle domain of Hsp90 regulates chaperone func-tion. Mol Cell, 2007, 25(1) : 151-159.
-
3Boyault C, Sadoul K, Pabion M, et al. HDAC6, at the crossroads between cytoskeleton and cell signaling by acetyla- tion and ubiquitination. Oncogene, 2007, 26 ( 37 ) : 5468 -5476.
-
4Haggarty SJ, Koeller KM, Wong JC, et al. Domain-selec- tive small- molecule inhibitor of histone dcacetylase 6 (HDAC6)-mediated tubulin deacetylation. Proc Natl Acad Sci U S A, 2003, 100(8) : 4389-4394.
-
5Haggarty SJ, Koeller KM, Wong JC, et al. Multidimensional chemical genetic analysis of diversity-oriented synthesis-de- rived deacetylase inhibitors using cell-based assays. Chem Bi- ol, 2003, 10(5) : 383-396.
-
6Chen B, Petukhov PA, Jung M, et al. Chemistry and biolo- gy of mercaptoacetamides as novel histone deacetylase inhibi- tors. Bioorg Med Chem Lett, 2005 , 15 ( 5 ) : 1389- 1392.
-
7hoh Y, Suzuki T, Miyata N. Isoform-selective histone deacetylase inhibitors. Curr Pharm Des, 2008 , 14 ( 6 ) : 529-544.
-
8Kozikowski AP, Chen Y, Gaysin A, et al. Functional differ- ences in epigenetic modulators-superiority of mercaptoacet- amide-based histone deacetylase inhibitors relative to hydrox- amates in cortical neuron neuroprotection studies. J Med Chem, 2007, 50(13) : 3054-3061.
-
9Kozikowski AP, Chen Y, Gaysin AM, et al. Chemistry, bi- ology, and QSAR studies of substituted biaryl hydroxamates and mercaptoacetamides as HDAC inhibitors-nanomolar-poten- cy inhibitors of pancreatic cancer cell growth. Chem Med Chem, 2008, 3(3) : 487-501.
-
10Itoh Y, Suzuki T, Kouketsu A, et al. Design, synthesis, structure--selectivity relationship, and effect on human cancer cells of a novel series of histone deacetylase 6- selective inhibi- tors. J Med Chem, 2007, 50(22) : 5425-5438.
同被引文献40
-
1秦永伟,程纯,王海波,高永静,邵晓轶,沈爱国.P38在LPS诱导大鼠雪旺氏(Schwann)细胞TNF-α表达中的作用[J].中国生物化学与分子生物学报,2007,23(5):382-387. 被引量:5
-
2Jope RS, Yuskaitis C J, Beurel E. Glycogen synthase kinase- 3 ( GSK3 ) : inflammation, diseases, and therapeutics. Neu- rochem Res, 2007, 32(4-5) : 577-595.
-
3Jo J, Whitcomb DJ, Olsen KM, et al. Aβ(1-42) inhibi- tion of LTP is mediated by a signaling pathway involving caspase-3, Aktl and GSK-3β. Nat Neurosci, 2011, 14 (5) : 545 -547.
-
4Ma T, Hoeffer CA, Capetillo-Zarate E, et al. Dysregulation of the mTOR pathway mediates impairment of synaptic plastici- ty in a mouse model of Alzheimer' s disease. PloS One, 2010, 5(9) : 12845.
-
5Muntane G, Dalfo E, Martinez A, et al. Phosphorylation of tan and alpha-synuclein in synaptic-enriched fractions of the frontal cortex in Alzheimer' s disease, and in Parkinson' s disease and related alpha-synueleinopathies. Neuroscience, 2008, 152(.4) : 913-923.
-
6Hye A, Kerr F, Archer N, et al. Glycogen synthase kinase- 3 is increased in white ceils early in Alzheimer' s disease. Neurosci Lett, 2005, 373(1) : 1-4.
-
7Zhang X, Heng X, Li T, et al. Long-term treatment with lithium alleviates memory deficits and reduces amyloid-β pro- duction in an aged Alzheimer' s disease transgenic mouse model. J Alzheimers Dis, 2011, 24(4): 739-749.
-
8De Samo P, Bijur GN, Zmijewska AA, et al. In vivo regu- lation of GSK3 phosphorylation by eholinergie and NMDA re- ceptors. Neurobiol Aging, 2006, 27(3): 413-422.
-
9Tyagarajan SK, Ghosh H, Yevenes GE, et al. Regulation of GABAergic synapse formation and plasticity by GSK3 beta-de- pendent phosphorylation of gephyrin. Proc Natl Acad Sci USA, 2011, 108(1) : 379-384.
-
10Zhou X, Zhou J, Li X. GSK-313 inhibitors suppressed neu- roinflammation in rat cortex by activating autophagy in ischemic brain injury. Biochem Biophys Res Commun, 2011 , 411 (2) : 271-275.
引证文献4
-
1范鸣玥,吕佩源.糖原合成酶激酶-3、锂剂和神经精神性疾病[J].国际神经病学神经外科学杂志,2013,40(1):98-100. 被引量:1
-
2赵娟,张彦妹,郑乃智.阿尔茨海默病和癫:神经变性与网络功能异常相关性研究进展[J].中国临床神经科学,2017,25(4):465-469. 被引量:1
-
3秦丽,宋远见,杨荣礼,李雷.HDAC6和p38信号分子在神经炎症中的研究现状[J].国际老年医学杂志,2018,39(1):40-44. 被引量:1
-
4孙素娟,刘学伍.组蛋白脱乙酰酶6在中枢神经系统疾病中作用的研究进展[J].国际神经病学神经外科学杂志,2023,50(3):84-90. 被引量:1
二级引证文献4
-
1唐皓月,李志芸,魏旋子,王旭,卢雪红.GSK-3β抑制剂对糖尿病肾病大鼠的作用研究[J].中国中西医结合肾病杂志,2017,18(11):950-952. 被引量:6
-
2钱园园,孙林琳,段淑荣.长链非编码RNA与阿尔茨海默病的相关性研究进展[J].中国临床神经科学,2019,27(6):700-704. 被引量:1
-
3王晴,夏建国,田为中.帕金森病伴认知功能损伤的静息态脑网络功能磁共振研究进展[J].磁共振成像,2020,11(11):1044-1047. 被引量:11
-
4汪紫微,梁艳,王运良,沈文清,戚慧,何标.运动调节组蛋白去乙酰化改善阿尔茨海默病的研究进展[J].生命的化学,2024,44(5):786-794.
-
1朱饮源,姚军,李曼.糖原合成酶激酶3β对卵巢癌紫杉醇耐药性的影响及机制研究[J].东南国防医药,2015,17(1):29-31. 被引量:1
-
2魏金龙,刘鸣,王苏亮,赵治明,杨艳,李晶,袁雪.喉癌组织糖原合成酶激酶3β、T细胞因子4表达及意义[J].山东医药,2016,56(28):60-62. 被引量:1
-
3王南瑶,王琼,费燕华,袁明,吴丹.Tau蛋白在胃癌中的表达及其临床意义[J].临床肿瘤学杂志,2012,17(2):135-137. 被引量:2
-
4王琼,王南瑶,邵国益,袁明,束永前,茅卫东.Tau蛋白对胃癌患者紫杉醇敏感性的预测[J].中国肿瘤临床与康复,2015,22(2):169-170. 被引量:1
-
5朱饮源,姚军,李曼.糖原合成酶激酶3β对卵巢癌顺铂耐药性的影响及其机制研究[J].南京医科大学学报(自然科学版),2015,35(3):332-336. 被引量:2
-
6何琼琼,程瑞雪,陈主初.蛋白质组学在肝癌研究中的应用[J].国外医学(肿瘤学分册),2005,32(10):782-784.
-
7陆颖影,靖大道,王兴鹏.表皮生长因子受体与胰腺癌的关系及以其为靶向治疗的研究进展[J].胃肠病学,2007,12(1):53-55. 被引量:1
-
8宋锦秋,陈晓春.MAPK信号通路与阿尔茨海默病中tau蛋白磷酸化的关系[J].国际神经病学神经外科学杂志,2006,33(4):339-343. 被引量:14
-
9刘欢,郭澍,唐明睿,孙强.GSK3β在病理性瘢痕中的表达和意义[J].中国美容整形外科杂志,2012,23(5):318-320. 被引量:2
-
10李志华,涂剑宏,龚宇,雷秋模,魏文嵩,罗永辉.Tau蛋白表达与ER阳性乳腺癌紫杉类化疗敏感性的临床分析[J].中国医药导报,2012,9(12):23-25. 被引量:2