Extensive soma-soma plate-like contact sites (ephapses) connect suprachiasmatic nucleus neurons

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Mark É. Czeisler, Yongli Shan, Richard Schalek, Daniel R. Berger, Adi Suissa-Peleg, Joseph S. Takahashi, Jeff W. Lichtman
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Abstract

The hypothalamic suprachiasmatic nucleus (SCN) is the central pacemaker for mammalian circadian rhythms. As such, this ensemble of cell-autonomous neuronal oscillators with divergent periods must maintain coordinated oscillations. To investigate ultrastructural features enabling such synchronization, 805 coronal ultrathin sections of mouse SCN tissue were imaged with electron microscopy and aligned into a volumetric stack, from which selected neurons within the SCN core were reconstructed in silico. We found that clustered SCN core neurons were physically connected to each other via multiple large soma-to-soma plate-like contacts. In some cases, a sliver of a glial process was interleaved. These contacts were large, covering on average ∼21% of apposing neuronal somata. It is possible that contacts may be the electrophysiological substrate for synchronization between SCN neurons. Such plate-like contacts may explain why the synchronization of SCN neurons is maintained even when chemical synaptic transmission or electrical synaptic transmission via gap junctions is blocked. Such ephaptic contact-mediated synchronization among nearby neurons may therefore contribute to the wave-like oscillations of circadian core clock genes and calcium signals observed in the SCN.

Abstract Image

广泛的体节-体节板状接触点(ephapses)连接着嗜上核神经元。
下丘脑丘上核(SCN)是哺乳动物昼夜节律的中心起搏器。因此,这个由具有不同周期的细胞自主神经元振荡器组成的集合体必须保持协调振荡。为了研究实现这种同步的超微结构特征,我们用电子显微镜对小鼠 SCN 组织的 805 个冠状超薄切片进行了成像,并将其排列成一个体积堆栈,从中对 SCN 核心内的部分神经元进行了硅学重建。我们发现,聚集在一起的 SCN 核心神经元通过多个大的体节-体节板状接触点彼此物理连接。在某些情况下,还夹杂着一片神经胶质过程。这些接触面很大,平均覆盖了21%的神经元体节。接触可能是SCN神经元间同步的电生理基质。这种板状接触可能解释了为什么即使通过间隙连接进行的化学突触传递或电突触传递被阻断,SCN 神经元之间的同步仍能保持。因此,这种由突触接触介导的邻近神经元之间的同步可能有助于在 SCN 中观察到的昼夜节律核心时钟基因和钙信号的波状振荡。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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