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驱动蛋白的多面性:从构建树突棘、稳定间隙连接到塑造神经突样细胞突起。

Many faces of drebrin: from building dendritic spines and stabilizing gap junctions to shaping neurite-like cell processes.

作者信息

Majoul Irina, Shirao Tomoaki, Sekino Yuko, Duden Rainer

机构信息

School of Biological Sciences, Royal Holloway, University of London, Egham, Surrey, TW20 0EX, UK.

出版信息

Histochem Cell Biol. 2007 Apr;127(4):355-61. doi: 10.1007/s00418-007-0273-y. Epub 2007 Feb 7.

DOI:10.1007/s00418-007-0273-y
PMID:17285341
Abstract

In this review we consider the multiple functions of developmentally regulated brain protein (drebrin), an actin-binding protein, in the formation of cellular polarity in different cell types. Drebrin has a well-established role in the morphogenesis, patterning and maintenance of dendritic spines in neurons. We have recently shown that drebrin also stabilizes Connexin-43 containing gap junctions at the plasma membrane. The latest literature and our own data suggest that drebrin may be broadly involved in shaping cell processes and in the formation of stabilized plasma membrane domains, an effect that is likely to be of crucial significance for formation of cell polarity in both neuronal and non-neuronal types.

摘要

在本综述中,我们探讨了发育调控脑蛋白(drebrin)(一种肌动蛋白结合蛋白)在不同细胞类型中细胞极性形成过程中的多种功能。Drebrin在神经元树突棘的形态发生、模式形成和维持方面具有既定作用。我们最近发现,drebrin还能稳定质膜上含连接蛋白43的间隙连接。最新文献和我们自己的数据表明,drebrin可能广泛参与细胞突起的塑造以及稳定质膜结构域的形成,这一作用对于神经元和非神经元类型细胞极性的形成可能具有至关重要的意义。

相似文献

1
Many faces of drebrin: from building dendritic spines and stabilizing gap junctions to shaping neurite-like cell processes.驱动蛋白的多面性:从构建树突棘、稳定间隙连接到塑造神经突样细胞突起。
Histochem Cell Biol. 2007 Apr;127(4):355-61. doi: 10.1007/s00418-007-0273-y. Epub 2007 Feb 7.
2
Drebrin is a novel connexin-43 binding partner that links gap junctions to the submembrane cytoskeleton.驱动蛋白是一种新型的连接蛋白43结合伴侣,它将间隙连接与膜下细胞骨架相连。
Curr Biol. 2004 Apr 20;14(8):650-8. doi: 10.1016/j.cub.2004.03.063.
3
Drebrins and Connexins: A Biomedical Perspective.drebrin蛋白与连接蛋白:生物医学视角
Adv Exp Med Biol. 2017;1006:225-247. doi: 10.1007/978-4-431-56550-5_13.
4
Drebrin A regulates dendritic spine plasticity and synaptic function in mature cultured hippocampal neurons.动力蛋白调节蛋白A调控成熟培养海马神经元中的树突棘可塑性和突触功能。
J Cell Sci. 2009 Feb 15;122(Pt 4):524-34. doi: 10.1242/jcs.033464. Epub 2009 Jan 27.
5
Drebrin and Spine Formation.肌动蛋白结合蛋白与脊柱形成
Adv Exp Med Biol. 2017;1006:157-181. doi: 10.1007/978-4-431-56550-5_10.
6
Drebrin at Junctional Plaques.连接斑处的 drebrin 蛋白
Adv Exp Med Biol. 2017;1006:313-328. doi: 10.1007/978-4-431-56550-5_18.
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Isoform-dependent Regulation of Drebrin Dynamics in Dendritic Spines.树突棘中 Drebrin 动力学的异构体依赖性调节
Neuroscience. 2018 May 21;379:67-76. doi: 10.1016/j.neuroscience.2018.02.038. Epub 2018 Mar 6.
8
Activity of the AMPA receptor regulates drebrin stabilization in dendritic spine morphogenesis.AMPA 受体的活性在树突棘形态发生过程中调节 drebrin 的稳定性。
J Cell Sci. 2009 Apr 15;122(Pt 8):1211-9. doi: 10.1242/jcs.043729.
9
Connexin43 Forms Supramolecular Complexes through Non-Overlapping Binding Sites for Drebrin, Tubulin, and ZO-1.连接蛋白43通过与 drebrin、微管蛋白和紧密连接蛋白1(ZO-1)的非重叠结合位点形成超分子复合物。
PLoS One. 2016 Jun 9;11(6):e0157073. doi: 10.1371/journal.pone.0157073. eCollection 2016.
10
Activation of N-methyl-D-aspartate receptor induces a shift of drebrin distribution: disappearance from dendritic spines and appearance in dendritic shafts.N-甲基-D-天冬氨酸受体的激活会导致drebrin分布的改变:从树突棘消失并出现在树突干中。
Mol Cell Neurosci. 2006 Mar;31(3):493-504. doi: 10.1016/j.mcn.2005.11.003. Epub 2005 Dec 20.

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Role of Actin-Binding Proteins in Skeletal Myogenesis.肌动蛋白结合蛋白在骨骼肌发生中的作用。
Cells. 2023 Oct 25;12(21):2523. doi: 10.3390/cells12212523.
2
Drebrin Regulates Acetylcholine Receptor Clustering and Organization of Microtubules at the Postsynaptic Machinery. drebrin 调节乙酰胆碱受体在突触后机制中的聚集和微管组织。
Int J Mol Sci. 2021 Aug 30;22(17):9387. doi: 10.3390/ijms22179387.
3
Evidence of decreased gap junction coupling between astrocytes and oligodendrocytes in the anterior cingulate cortex of depressed suicides.

本文引用的文献

1
Dynamics of the actin-binding protein drebrin in motile cells and definition of a juxtanuclear drebrin-enriched zone.肌动蛋白结合蛋白drebrin在运动细胞中的动态变化及近核富含drebrin区域的定义
Exp Cell Res. 2006 Aug 1;312(13):2605-18. doi: 10.1016/j.yexcr.2006.04.017. Epub 2006 May 11.
2
Down-regulation of drebrin A expression suppresses synaptic targeting of NMDA receptors in developing hippocampal neurones.脑发育蛋白A表达的下调会抑制发育中的海马神经元中NMDA受体的突触靶向。
J Neurochem. 2006 Apr;97 Suppl 1:110-5. doi: 10.1111/j.1471-4159.2005.03536.x.
3
Drebrin, an actin-binding, cell-type characteristic protein: induction and localization in epithelial skin tumors and cultured keratinocytes.
抑郁自杀者扣带回皮质前部星形胶质细胞和少突胶质细胞之间缝隙连接偶联减少的证据。
Neuropsychopharmacology. 2019 Nov;44(12):2099-2111. doi: 10.1038/s41386-019-0471-z. Epub 2019 Aug 2.
4
Drebrin and Spermatogenesis.drebrin与精子发生
Adv Exp Med Biol. 2017;1006:291-312. doi: 10.1007/978-4-431-56550-5_17.
5
Role of Drebrin at the Immunological Synapse.drebrin在免疫突触中的作用。
Adv Exp Med Biol. 2017;1006:271-280. doi: 10.1007/978-4-431-56550-5_15.
6
Drebrin-mediated microtubule-actomyosin coupling steers cerebellar granule neuron nucleokinesis and migration pathway selection.Drebrin 通过介导微管-肌动蛋白偶联来控制小脑颗粒神经元的核迁移,并选择迁移路径。
Nat Commun. 2017 Feb 23;8:14484. doi: 10.1038/ncomms14484.
7
Investigation of hippocampal synaptic transmission and plasticity in mice deficient in the actin-binding protein Drebrin.研究肌动蛋白结合蛋白 Drebrin 缺失小鼠海马突触传递和可塑性。
Sci Rep. 2017 Feb 15;7:42652. doi: 10.1038/srep42652.
8
Connexin43 Forms Supramolecular Complexes through Non-Overlapping Binding Sites for Drebrin, Tubulin, and ZO-1.连接蛋白43通过与 drebrin、微管蛋白和紧密连接蛋白1(ZO-1)的非重叠结合位点形成超分子复合物。
PLoS One. 2016 Jun 9;11(6):e0157073. doi: 10.1371/journal.pone.0157073. eCollection 2016.
9
Lens ion homeostasis relies on the assembly and/or stability of large connexin 46 gap junction plaques on the broad sides of differentiating fiber cells.晶状体离子动态平衡依赖于大的缝隙连接蛋白 46 在分化纤维细胞宽大胞侧的组装和/或稳定。
Am J Physiol Cell Physiol. 2015 May 15;308(10):C835-47. doi: 10.1152/ajpcell.00372.2014. Epub 2015 Mar 4.
10
A reduction in Npas4 expression results in delayed neural differentiation of mouse embryonic stem cells.Npas4表达的降低导致小鼠胚胎干细胞的神经分化延迟。
Stem Cell Res Ther. 2014 May 8;5(3):64. doi: 10.1186/scrt453.
肌动蛋白结合蛋白德雷布林,一种细胞类型特异性蛋白:在上皮性皮肤肿瘤和培养的角质形成细胞中的诱导与定位
J Invest Dermatol. 2005 Oct;125(4):761-74. doi: 10.1111/j.0022-202X.2005.23793.x.
4
The origin recognition core complex regulates dendrite and spine development in postmitotic neurons.起源识别核心复合体调控有丝分裂后神经元的树突和棘突发育。
J Cell Biol. 2005 Aug 15;170(4):527-35. doi: 10.1083/jcb.200505075. Epub 2005 Aug 8.
5
Overexpression of drebrin A in immature neurons induces the accumulation of F-actin and PSD-95 into dendritic filopodia, and the formation of large abnormal protrusions.未成熟神经元中肌动蛋白结合蛋白A的过表达会诱导丝状肌动蛋白和突触后致密蛋白95在树突丝状伪足中积累,并形成大量异常突起。
Mol Cell Neurosci. 2005 Sep;30(1):149-57. doi: 10.1016/j.mcn.2005.06.008.
6
Polarity proteins in axon specification and synaptogenesis.轴突特化和突触形成中的极性蛋白。
Dev Cell. 2005 Jun;8(6):803-16. doi: 10.1016/j.devcel.2005.05.007.
7
Foot and mouth: podosomes, invadopodia and circular dorsal ruffles.口蹄疫:足体、侵袭性伪足和环形背侧褶皱
Nat Rev Mol Cell Biol. 2004 Aug;5(8):647-57. doi: 10.1038/nrm1436.
8
Connexins: functions without junctions.连接蛋白:无连接结构的功能。
Curr Opin Cell Biol. 2004 Oct;16(5):507-12. doi: 10.1016/j.ceb.2004.07.014.
9
The sequential activity of the GTPases Rap1B and Cdc42 determines neuronal polarity.GTP酶Rap1B和Cdc42的顺序活性决定神经元极性。
Nat Neurosci. 2004 Sep;7(9):923-9. doi: 10.1038/nn1295. Epub 2004 Aug 1.
10
Antisense knockdown of drebrin A, a dendritic spine protein, causes stronger preference, impaired pre-pulse inhibition, and an increased sensitivity to psychostimulant.对树突棘蛋白drebrin A进行反义敲低,会导致更强的偏好、前脉冲抑制受损以及对精神兴奋剂的敏感性增加。
Neurosci Res. 2004 Jun;49(2):205-17. doi: 10.1016/j.neures.2004.02.014.