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The Astrocyte Nexus: CX43-Protein Interactions

The Astrocyte Nexus: CX43-Protein Interactions
星形胶质细胞关系:CX43-蛋白质相互作用
批准号:
8048968
负责人:
David C Spray
金额:
$35.59万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-12-15 至 2013-03-31

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英文摘要
DESCRIPTION (provided by applicant): Long range intercellular communication among astrocytes is in large part mediated by gap junction channels, through which ions and metabolites pass directly from one cell to the next. The pore of astrocyte gap junctions is formed primarily of the gap junction protein connexin43 (Cx43). Recent evidence indicates that other proteins are associated with Cx43 at gap junctions, forming a macromolecular complex that we have termed the Nexus. We hypothesize that the Nexus components may regulate both the properties of the gap junction channels and also may function in intracellular signal transduction and trafficking of Cx43 within the astrocyte, all of which are critical for maintaining the network of coupled astrocytes throughout the brain. During the last period of support, we found that both intra- and intermolecular interactions occur with Cx43, have quantified the affinities of several interactions under different pH and phosphorylation conditions and used NMR to solve structures of relevant Cx43 cytoplasmic domains and to determine how structures change upon binding. We have also identified new binding partners for Cx43 and have begun to examine how interaction with binding partners affects function of Cx43 gap junction channels and the intracellular trafficking of this protein to and from the membrane. The Nexus complex in astrocytes is thus dynamic, changing binding partner affinities due to local conditions and local concentrations of ligands. We now propose to extend these studies to determine how interactions of cytoskeletal proteins with Cx43 is linked to both rapid and gradual remodeling of the astrocyte network. The proposed studies use an interdisciplinary approach with several techniques that are new to the gap junction field to rigorously explore the novel concept that connexin-cytoskeletal interaction is a major determinant of gap junction function in astrocytes. As such, these studies are expected to lead to novel insight of roles that gap junctions play in the nervous system and elsewhere.
期刊论文(17)
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会议论文
Transcriptome profiling of hippocampal CA1 after early-life seizure-induced preconditioning may elucidate new genetic therapies for epilepsy.
早期癫痫发作引起的预处理后,海马CA1的转录组分析可能阐明新的基因疗法癫痫。
DOI: 10.1111/ejn.12168
发表时间: 2013-07
期刊: The European journal of neuroscience
影响因子: --
作者: [Friedman LK, Mancuso J, Patel A, Kudur V, Leheste JR, Iacobas S, Botta J, Iacobas DA, Spray DC]
通讯作者: Spray DC
DOI: 10.1007/s00221-008-1523-5
发表时间: 2008-11
期刊: EXPERIMENTAL BRAIN RESEARCH
影响因子: 2
作者: [Frigeri, Antonio, Iacobas, Dumitru A., Iacobas, Sanda, Nicchia, Grazia Paola, Desaphy, Jean Francois, Camerino, Diana Conte, Svelto, Maria, Spray, David C.]
通讯作者: Spray, David C.
Fluid flow-induced soluble vascular endothelial growth factor isoforms regulate actin adaptation in osteoblasts.
流体流动诱导的可溶性血管内皮生长因子亚型调节成骨细胞中的肌动蛋白适应。
DOI: 10.1074/jbc.m110.114975
发表时间: 2010
期刊: The Journal of biological chemistry
影响因子: --
作者: [Thi,MiaM, Suadicani,SylviaO, Spray,DavidC]
通讯作者: Spray,DavidC
DOI: 10.1042/an20090001
发表时间: 2009-04-14
期刊: ASN neuro
影响因子: 4.7
作者: [Suadicani SO, Iglesias R, Spray DC, Scemes E]
通讯作者: Scemes E
11
    THE IMPACT OF HYPOXIA ON DEVELOPMENT AND REMODELING OF CARDIC INTERCALATED DISK
    Luminescence Imaging: Molecules, Cells and Tissues
    Neuronal Gap Junctions: Cx36 Gating, Binding & Function
    Neuronal Gap Junctions: Cx36 Gating, Binding & Function
    海外基金