突触成分的长循环回收(LLR)是一个经济学问题

IF 2.6 3区 医学 Q3 NEUROSCIENCES Molecular and Cellular Neuroscience Pub Date : 2023-09-01 DOI:10.1016/j.mcn.2023.103862
Svilen Veselinov Georgiev , Silvio O. Rizzoli
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引用次数: 0

摘要

突触前和突触后隔室包含各种已知在质膜和细胞内细胞器之间循环的分子。循环步骤已在功能方面得到充分描述,例如,突触小泡循环对神经递质释放至关重要,突触后受体循环是突触可塑性的基本特征。然而,突触蛋白回收也可能发挥更为平淡的作用,简单地确保特定成分的重复使用,从而最大限度地减少突触蛋白合成的能量消耗。最近已经描述了这种类型的过程,用于细胞外基质的成分,其经历长环循环(LLR),往返于细胞体。在这里,我们认为突触成分的节能回收可能比人们普遍认为的更广泛,可能在突触小泡蛋白的使用和突触后受体代谢中发挥作用。
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The long-loop recycling (LLR) of synaptic components as a question of economics

The pre- and post-synaptic compartments contain a variety of molecules that are known to recycle between the plasma membrane and intracellular organelles. The recycling steps have been amply described in functional terms, with, for example, synaptic vesicle recycling being essential for neurotransmitter release, and postsynaptic receptor recycling being a fundamental feature of synaptic plasticity. However, synaptic protein recycling may also serve a more prosaic role, simply ensuring the repeated use of specific components, thereby minimizing the energy expenditure on the synthesis of synaptic proteins. This type of process has been recently described for components of the extracellular matrix, which undergo long-loop recycling (LLR), to and from the cell body. Here we suggest that the energy-saving recycling of synaptic components may be more widespread than is generally acknowledged, potentially playing a role in both synaptic vesicle protein usage and postsynaptic receptor metabolism.

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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
65
审稿时长
37 days
期刊介绍: Molecular and Cellular Neuroscience publishes original research of high significance covering all aspects of neurosciences indicated by the broadest interpretation of the journal''s title. In particular, the journal focuses on synaptic maintenance, de- and re-organization, neuron-glia communication, and de-/regenerative neurobiology. In addition, studies using animal models of disease with translational prospects and experimental approaches with backward validation of disease signatures from human patients are welcome.
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