Furusawa Kotaro, Emoto Kazuo
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.
International Research Center for Neurointelligence (WPI-IRCN), The University of Tokyo, Tokyo, Japan.
Front Cell Neurosci. 2021 Jan 11;14:613320. doi: 10.3389/fncel.2020.613320. eCollection 2020.
Dendrites are cellular structures essential for the integration of neuronal information. These elegant but complex structures are highly patterned across the nervous system but vary tremendously in their size and fine architecture, each designed to best serve specific computations within their networks. Recent imaging studies reveal that the development of mature dendrite arbors in many cases involves extensive remodeling achieved through a precisely orchestrated interplay of growth, degeneration, and regeneration of dendritic branches. Both degeneration and regeneration of dendritic branches involve precise spatiotemporal regulation for the proper wiring of functional networks. In particular, dendrite degeneration must be targeted in a compartmentalized manner to avoid neuronal death. Dysregulation of these developmental processes, in particular dendrite degeneration, is associated with certain types of pathology, injury, and aging. In this article, we review recent progress in our understanding of dendrite degeneration and regeneration, focusing on molecular and cellular mechanisms underlying spatiotemporal control of dendrite remodeling in neural development. We further discuss how developmental dendrite degeneration and regeneration are molecularly and functionally related to dendrite remodeling in pathology, disease, and aging.
树突是整合神经元信息所必需的细胞结构。这些优雅却复杂的结构在整个神经系统中具有高度的模式化,但它们的大小和精细结构却差异极大,每一种都旨在最有效地服务于其所在网络内的特定计算。最近的成像研究表明,在许多情况下,成熟树突分支的发育涉及广泛的重塑,这是通过树突分支的生长、退化和再生之间精确协调的相互作用实现的。树突分支的退化和再生都涉及精确的时空调节,以实现功能网络的正确布线。特别是,树突退化必须以分区的方式进行靶向,以避免神经元死亡。这些发育过程的失调,尤其是树突退化,与某些类型的病理、损伤和衰老有关。在本文中,我们综述了我们对树突退化和再生理解的最新进展,重点关注神经发育中树突重塑时空控制的分子和细胞机制。我们还将进一步讨论发育性树突退化和再生在分子和功能上如何与病理、疾病和衰老中的树突重塑相关。