Echinoderm radial glia in adult cell renewal, indeterminate growth, and regeneration.

IF 3.4 3区 医学 Q2 NEUROSCIENCES Frontiers in Neural Circuits Pub Date : 2023-09-29 eCollection Date: 2023-01-01 DOI:10.3389/fncir.2023.1258370
Vladimir Mashanov, Soji Ademiluyi, Denis Jacob Machado, Robert Reid, Daniel Janies
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Abstract

Echinoderms are a phylum of marine deterostomes with a range of interesting biological features. One remarkable ability is their impressive capacity to regenerate most of their adult tissues, including the central nervous system (CNS). The research community has accumulated data that demonstrates that, in spite of the pentaradial adult body plan, echinoderms share deep similarities with their bilateral sister taxa such as hemichordates and chordates. Some of the new data reveal the complexity of the nervous system in echinoderms. In terms of the cellular architecture, one of the traits that is shared between the CNS of echinoderms and chordates is the presence of radial glia. In chordates, these cells act as the main progenitor population in CNS development. In mammals, radial glia are spent in embryogenesis and are no longer present in adults, being replaced with other neural cell types. In non-mammalian chordates, they are still detected in the mature CNS along with other types of glia. In echinoderms, radial glia also persist into the adulthood, but unlike in chordates, it is the only known glial cell type that is present in the fully developed CNS. The echinoderm radial glia is a multifunctional cell type. Radial glia forms the supporting scaffold of the neuroepithelium, exhibits secretory activity, clears up dying or damaged cells by phagocytosis, and, most importantly, acts as a major progenitor cell population. The latter function is critical for the outstanding developmental plasticity of the adult echinoderm CNS, including physiological cell turnover, indeterminate growth, and a remarkable capacity to regenerate major parts following autotomy or traumatic injury. In this review we summarize the current knowledge on the organization and function of the echinoderm radial glia, with a focus on the role of this cell type in adult neurogenesis.

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棘皮放射状胶质细胞在成体细胞更新、不确定生长和再生中的作用。
棘皮动物是一个具有一系列有趣生物学特征的海洋动物门。一个显著的能力是它们令人印象深刻的再生大部分成年组织的能力,包括中枢神经系统(CNS)。研究界积累的数据表明,尽管棘皮动物的成体计划是五径形的,但它们与半脊索动物和脊索动物等双边姐妹类群有着深刻的相似之处。一些新数据揭示了棘皮动物神经系统的复杂性。就细胞结构而言,棘皮动物和脊索动物的中枢神经系统共有的特征之一是存在放射状胶质细胞。在脊索动物中,这些细胞是中枢神经系统发育的主要祖细胞群体。在哺乳动物中,放射状胶质细胞用于胚胎发生,在成年后不再存在,取而代之的是其他类型的神经细胞。在非哺乳动物脊索动物中,它们仍然与其他类型的神经胶质一起在成熟的中枢神经系统中被检测到。在棘皮动物中,放射状胶质细胞也会持续到成年,但与脊索动物不同,它是唯一已知的存在于完全发育的中枢神经系统中的胶质细胞类型。棘皮动物放射状胶质细胞是一种多功能的细胞类型。放射状胶质细胞形成神经上皮的支撑支架,表现出分泌活性,通过吞噬作用清除垂死或受损的细胞,最重要的是,作为主要的祖细胞群体。后一种功能对于成年棘皮动物中枢神经系统突出的发育可塑性至关重要,包括生理细胞更新、不确定的生长以及在自残或创伤后再生主要部分的显著能力。在这篇综述中,我们总结了棘皮动物桡神经胶质的组织和功能的最新知识,重点是这种细胞类型在成人神经发生中的作用。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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