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补体系统作为中枢神经系统内稳态、神经突触可塑性和认知功能的主要调节者而出现。

Complement emerges as a masterful regulator of CNS homeostasis, neural synaptic plasticity and cognitive function.

机构信息

Division of Biodiagnostic Sciences and Technologies, INRASTES, National Center for Scientific Research 'Demokritos', Aghia Paraskevi Attikis, 15310 Athens, Greece.

出版信息

Exp Neurol. 2014 Nov;261:469-74. doi: 10.1016/j.expneurol.2014.06.019. Epub 2014 Jun 26.

Abstract

Growing evidence points to a previously elusive role of complement-modulated pathways in CNS development, neurogenesis and synaptic plasticity. Distinct complement effectors appear to play a multifaceted role in brain homeostasis by regulating synaptic pruning in the retinogeniculate system and sculpting functional neural circuits both in the developing and adult mammalian brain. A recent study by Perez-Alcazar et al. (2014) provides novel insights into this intricate interplay between complement and the dynamically regulated brain synaptic circuitry, by reporting that mice deficient in C3 exhibit enhanced hippocampus-dependent spatial learning and cognitive performance. This behavioral pattern is associated with an impact of C3 on the functional capacity of glutamatergic synapses, supporting a crucial role for complement in excitatory synapse elimination in the hippocampus. These findings add a fresh twist to this rapidly evolving research field, suggesting that discrete complement components may differentially modulate synaptic connectivity by wiring up with diverse neural effectors in different regions of the brain. The emerging role of complement in synaptogenesis and neural network plasticity opens new conceptual avenues for considering complement interception as a potential therapeutic modality for ameliorating progressive cognitive impairment in age-related, debilitating brain diseases with a prominent inflammatory signature.

摘要

越来越多的证据表明,补体调节途径在中枢神经系统发育、神经发生和突触可塑性中发挥着以前难以捉摸的作用。不同的补体效应物似乎通过调节视网膜-视交叉系统中的突触修剪以及在发育中和成年哺乳动物大脑中塑造功能性神经回路,在大脑稳态中发挥着多方面的作用。最近,Perez-Alcazar 等人的一项研究(2014 年)提供了关于补体与动态调节的大脑突触回路之间这种复杂相互作用的新见解,该研究报告称,C3 缺乏的小鼠表现出增强的海马依赖性空间学习和认知表现。这种行为模式与 C3 对谷氨酸能突触功能能力的影响有关,支持补体在海马兴奋性突触消除中的关键作用。这些发现为这个快速发展的研究领域增添了新的变化,表明离散的补体成分可能通过与大脑不同区域的不同神经效应器连接,以不同的方式调节突触连接。补体在突触发生和神经网络可塑性中的新兴作用为将补体阻断视为改善具有明显炎症特征的与年龄相关的进行性认知障碍的潜在治疗方法开辟了新的概念途径。

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