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轴突侧支与脑状态

Axon Collaterals and Brain States.

作者信息

Rockland Kathleen S

机构信息

Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, MA, United States.

出版信息

Front Syst Neurosci. 2018 Jul 17;12:32. doi: 10.3389/fnsys.2018.00032. eCollection 2018.

DOI:10.3389/fnsys.2018.00032
PMID:30065635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6056639/
Abstract

Multiple mechanisms have been identified as relevant to plasticity, functional stability, and reliable processing across brain states. In the context of stability under "ever-changing conditions" (this Topic), the role of axons has been relatively under-investigated. The highly branched topologies of many axons, however, seem well designed to differentially recruit and regulate distributed postsynaptic groups, possibly in a state-dependent fashion. In this Perspective, I briefly discuss several examples of axon collateralization, and then some of the branch-specific features that might subserve differential recruitment and whole brain activation. An emerging principle is that the number of collaterals and number of target structures are not stereotyped. Rather, axons originating from one defined source typically send branches to diversified subsets of target areas. This could achieve heterogeneous inputs, with different degrees of synchronicity. Variability of neuronal responses has been suggested as inversely proportional to the degree of temporally correlated input. Increased input homogeneity, driven by sensory stimulation or behavioral conditions, is reported to reduce neuronal variability, with axon collateralization potentially having an important role.

摘要

多种机制已被确定与大脑不同状态下的可塑性、功能稳定性及可靠处理过程相关。在“不断变化的条件”下的稳定性背景下(本专题),轴突的作用相对研究较少。然而,许多轴突高度分支的拓扑结构似乎经过精心设计,能够以可能依赖于状态的方式,差异性地募集和调节分布的突触后群体。在本观点中,我简要讨论了轴突侧支化的几个例子,然后探讨了一些可能有助于差异性募集和全脑激活的分支特异性特征。一个新出现的原则是,侧支数量和目标结构数量并非固定不变。相反,源自一个确定来源的轴突通常会向目标区域的多样化子集发送分支。这可以实现具有不同同步程度的异质性输入。有研究表明,神经元反应的变异性与时间相关输入的程度成反比。据报道,由感觉刺激或行为条件驱动的输入同质性增加会降低神经元变异性,轴突侧支化可能在其中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a4/6056639/cd4eeaa41b8e/fnsys-12-00032-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a4/6056639/557f85d05191/fnsys-12-00032-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a4/6056639/cd4eeaa41b8e/fnsys-12-00032-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a4/6056639/557f85d05191/fnsys-12-00032-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29a4/6056639/cd4eeaa41b8e/fnsys-12-00032-g0002.jpg

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