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Eph/ephrin对树突棘的调控与中枢神经系统疾病 被引量:1

The Regulation of Eph/ephrin to the Dendritic Spine and Central Nervous System Diseases
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摘要 树突棘是神经元树突上的功能性突起结构,通常作为突触后成份与投射来的轴突共同构成完整的突触连接。树突棘的形态与结构具有明显的可塑性,其变化通常会引起突触功能的改变。Eph受体酪氨酸激酶家族分子与其配体ephrin都是重要的神经导向因子,同时对树突棘结构也有直接的调控作用。Eph受体的活化可以促进树突棘的发生并影响树突棘的形态及内部结构;而Eph受体的异常也往往会损害正常的突触功能,甚至导致许多与树突棘结构异常相关的神经系统病变的发生。 Dendritic spines are functional protrusions on neuron dendrites and generally act as postsynaptlc sites to form integral synapses with axon terminals. In mature central nervous system, dendritic spines are often in motility and variations of spine morphology and structure can largely influence the function of synapses. Eph receptor tyrosine kinase family and its ephrin ligand family are important axon guidance cues and also directly regulate dendritic spines. It has been widely established that activation of Eph receptors by ephrins promotes spine mature as well as affect spine morphology and structure. The abnormality of Eptdephrin, however, generally impairs the synaptic function and results in several spine dysfunction-associated neural diseases.
作者 蒋宁 张红锋
出处 《细胞生物学杂志》 CSCD 2006年第4期527-529,共3页 Chinese Journal of Cell Biology
关键词 Eph/ephrin 树突棘 突触 可塑性 Eph/ephrin dendritic spines synapses plasticity
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参考文献25

  • 1Flanagan JG et al.Annu Rev Neurosci,1998,21:309
  • 2Palmer A et al.Genes Dev,2003,17:1429
  • 3Murai KK et al.Neuroscientist,2004,10:304
  • 4Bonhoeffer T et al.Neuron,2002,35:1019
  • 5Yuste R et al.Annu Rev Neurosci,2001,24:1071
  • 6Matus A.Science.2000,290:754
  • 7Lamprecht R et al.Nat Rev Neurosci,2004,5:45
  • 8Ethell IM et al.Neuron,2001,31:1001
  • 9Henkemeyer M et al.J Cell Biol,2003,163:1313
  • 10Penzes P et al.Neuron,2003,37:263

同被引文献24

  • 1张妍,唐民科,张均田.树突棘与学习记忆[J].国际神经病学神经外科学杂志,2006,33(4):312-315. 被引量:6
  • 2陈枝芳,徐亮,陆佩华.MARCKS及其对树突棘形态的维持作用[J].医学分子生物学杂志,2006,3(5):394-396. 被引量:1
  • 3柳春雨,陈康宁,段炜,刘国军,郑霁.局灶性脑缺血再灌注认知功能变化的实验研究[J].第三军医大学学报,2006,28(19):1976-1978. 被引量:2
  • 4Kim Y, Sung JY, Ceglia I, et al. Phosphorylation of WAVE1 regu- lates actin polymerization and dendritic spine morphology. Nature, 2006,442(7104) :814-817.
  • 5Soderling SH,Guire ES,Kaech S,et al. A WAVE-1 and WRP signa- ling complex regulates spine density, synaptic plasticity, and memo- ry. J Neurosci,2007,27(2) :355-365.
  • 6Ivanov A,Esclapez M,Pellegrino C,et al. Drebrin A regulates den- dritic spine plasticity and synaptic function in mature cultured hipp- ocampal neurons. J Cell Sci,2009,122(4) :524-534.
  • 7C-ielen M, Sieqler Retchless BS, Mony L, et al. Mechanism of differ- ential control of NMDA receptor activity by NR2 subunits. Nature, 2009,459 (7247) :703-707.
  • 8Yashiro K, Philpot BD. Regulation of NMDA receptor subunit ex- pression and its implications for LTD, LTP, and metaplasticity. J Neuropharmacol, 2008,55 ( 7 ) : 1081-1094.
  • 9Geraldo S,Khanzada UK,Parsons M,et al. Targeting of the F-actin- binding protein drebrin by the microtubule plus-tip protein EB3 is re- qulred for neuritol~enesis. Nat Cell Biol.2008.10 (10) :1181-1189.
  • 10Brown CE, Li P, Boyd JD, et al. Extensive turnover of dendritic spines and vascular remodeling in cortical tissues recovering from stroke. J Neurosci,2007,27 ( 15 ) :4101-4109.

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