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首页> 外文期刊>Annals of anatomy =: Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft >Synaptopodin and the spine apparatus organelle-Regulators of different forms of synaptic plasticity?
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Synaptopodin and the spine apparatus organelle-Regulators of different forms of synaptic plasticity?

机译:突触足蛋白和不同形式的突触可塑性的脊柱器细胞器调节剂?

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摘要

Synaptopodin (SP) is an actin-binding molecule, which is closely linked with the spine apparatus organelle (SA). Recent experimental evidence suggests that SP containing spines differ in their functional and structural properties from neighboring spines, which do not contain SP. These studies revealed for the first time that SP clusters colocalize with a functional internal source of calcium, which affects synaptic plasticity. Strikingly, SP-cluster associated calcium surges were shown to control synaptic strength in two ways: a ryanodine receptor (RyR) dependent potentiation of synaptic strength was reported, as well as inositol-triphosphate-receptor (IP3R) dependent depression. These results suggested that the SA is an important component of the molecular machinery controlling the calcium-dependent accumulation of AMPA-receptors (AMPA-R) at excitatory synapses. They raise the intriguing possibility that SP/SA could play a role in different forms of synaptic plasticity.
机译:Synaptopodin(SP)是一种肌动蛋白结合分子,与脊柱器细胞器(SA)紧密相连。最近的实验证据表明,含SP的棘与邻近的不含SP的棘的功能和结构性质不同。这些研究首次揭示SP团簇与功能性内部钙源共定位,从而影响突触可塑性。令人惊讶的是,SP簇相关的钙激增被证明以两种方式控制突触强度:据报道,莱丹碱受体(RyR)依赖于突触强度的增强,以及肌醇三磷酸受体(IP3R)依赖的抑郁。这些结果表明,SA是控制兴奋性突触中钙依赖性AMPA受体(AMPA-R)积累的分子机制的重要组成部分。他们提出了SP / SA可能在不同形式的突触可塑性中发挥作用的有趣可能性。

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