Timing of neuronal plasticity in development and aging.

Q1 Biochemistry, Genetics and Molecular Biology Wiley Interdisciplinary Reviews: Developmental Biology Pub Date : 2018-03-01 Epub Date: 2017-11-15 DOI:10.1002/wdev.305
Evguenia Ivakhnitskaia, Ryan Weihsiang Lin, Kana Hamada, Chieh Chang
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引用次数: 8

Abstract

Molecular oscillators are well known for their roles in temporal control of some biological processes like cell proliferation, but molecular mechanisms that provide temporal control of differentiation and postdifferentiation events in cells are less understood. In the nervous system, establishment of neuronal connectivity during development and decline in neuronal plasticity during aging are regulated with temporal precision, but the timing mechanisms are largely unknown. Caenorhabditis elegans has been a preferred model for aging research and recently emerges as a new model for the study of developmental and postdevelopmental plasticity in neurons. In this review we discuss the emerging mechanisms in timing of developmental lineage progression, axon growth and pathfinding, synapse formation, and reorganization, and neuronal plasticity in development and aging. We also provide a current view on the conserved core axon regeneration molecules with the intention to point out potential regulatory points of temporal controls. We highlight recent progress in understanding timing mechanisms that regulate decline in regenerative capacity, including progressive changes of intrinsic timers and co-opting the aging pathway molecules. WIREs Dev Biol 2018, 7:e305. doi: 10.1002/wdev.305 This article is categorized under: Invertebrate Organogenesis > Worms Establishment of Spatial and Temporal Patterns > Regulation of Size, Proportion, and Timing Nervous System Development > Worms Gene Expression and Transcriptional Hierarchies > Regulatory RNA.

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发育和衰老过程中神经元可塑性的时序。
众所周知,分子振荡器在细胞增殖等生物过程的时间控制中发挥着重要作用,但对细胞分化和后分化事件的时间控制的分子机制却知之甚少。在神经系统中,发育过程中神经元连通性的建立和衰老过程中神经元可塑性的下降受到时间精度的调节,但其时间机制在很大程度上是未知的。秀丽隐杆线虫一直是衰老研究的首选模型,最近成为研究神经元发育和发育后可塑性的新模型。在这篇综述中,我们讨论了在发育谱系进展、轴突生长和寻路、突触形成和重组以及发育和衰老中的神经元可塑性方面的新机制。我们还提供了保守的核心轴突再生分子的当前观点,旨在指出时间控制的潜在调控点。我们强调了最近在理解调节再生能力下降的定时机制方面的进展,包括内在计时器的渐进式变化和衰老途径分子的选择。生物工程学报,2018,37(4):391 - 391。doi: 10.1002 / wdev.305本文分类为:无脊椎动物器官发生>蠕虫时空模式的建立>神经系统发育的大小、比例和时间调控>蠕虫基因表达和转录层次>调控RNA。
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期刊介绍: Developmental biology is concerned with the fundamental question of how a single cell, the fertilized egg, ultimately produces a complex, fully patterned adult organism. This problem is studied on many different biological levels, from the molecular to the organismal. Developed in association with the Society for Developmental Biology, WIREs Developmental Biology will provide a unique interdisciplinary forum dedicated to fostering excellence in research and education and communicating key advances in this important field. The collaborative and integrative ethos of the WIREs model will facilitate connections to related disciplines such as genetics, systems biology, bioengineering, and psychology. The topical coverage of WIREs Developmental Biology includes: Establishment of Spatial and Temporal Patterns; Gene Expression and Transcriptional Hierarchies; Signaling Pathways; Early Embryonic Development; Invertebrate Organogenesis; Vertebrate Organogenesis; Nervous System Development; Birth Defects; Adult Stem Cells, Tissue Renewal and Regeneration; Cell Types and Issues Specific to Plants; Comparative Development and Evolution; and Technologies.
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