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首页> 外文期刊>Current opinion in neurology >Cilia in the nervous system: linking cilia function and neurodevelopmental disorders.
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Cilia in the nervous system: linking cilia function and neurodevelopmental disorders.

机译:神经系统中的纤毛:将纤毛功能与神经发育障碍联系在一起。

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PURPOSE OF REVIEW: Ciliopathies are genetic disorders caused by defects of primary ciliary structure and/or function and are characterized by pleiotropic clinical features. The ciliopathies include several partially overlapping syndromes such as Joubert syndrome, Bardet-Biedl syndrome and Meckel-Gruber syndrome, all of which have pronounced neurodevelopmental features. Here we focus on potential roles of cilia in central nervous system function, to explore how impairments may cause brain malformation and neurodevelopmental disease. RECENT FINDINGS: Cilia have long been considered as 'sensory cellular antennae', responding as chemo-sensors, mechano-sensors and thermo-sensors, although their roles in development were not well understood until recently. The surprising finding that disparate syndromes are all due to defects of the primary cilia, along with the recent advances in genetics, has helped elucidate further roles of primary cilia beyond sensory functions. Several molecules that are associated with key signaling pathways have been discovered in primary cilia. These include sonic hedgehog, wingless, planar cell polarity and fibroblast growth factor, which are essential for many cellular processes. Additionally, mutations in 'ciliome' genes have largely shown developmental defects such as abnormal body axis and brain malformation, implying disrupted cilia-related signaling pathways. Accordingly, the emerging theme is that primary cilia may play roles as modulators of signal transduction to help shape cellular responses within the environmental context during both development and homeostasis. SUMMARY: The link between cilia and signal pathways has become a framework for understanding the pathogenesis of ciliopathies. Despite recent progress in ciliary biology, fundamental questions remain about how cilia regulate neuronal function in the central nervous system. Therefore, investigation of ciliary function in the nervous system may reveal cilia-modulating mechanisms in neurodevelopmental processes, as well as suggest new treatments for disease.
机译:审查目的:脊髓型颈椎病是由初级睫状结构和/或功能缺陷引起的遗传性疾病,其特征是多效性临床特征。纤毛虫病包括一些部分重叠的综合症,例如Joubert综合症,Bardet-Biedl综合症和Meckel-Gruber综合症,所有这些都具有明显的神经发育特征。在这里,我们专注于纤毛在中枢神经系统功能中的潜在作用,以探讨损伤可能如何导致脑畸形和神经发育疾病。最近的发现:尽管直到最近,人们才对纤毛在化学传感器,机械传感器和热传感器中的作用作出反应,但它们一直被认为是“感觉细胞触角”。令人惊讶的发现是,完全不同的综合征都是由于原发纤毛的缺陷所致,以及遗传学的最新进展,这有助于阐明原发纤毛在感觉功能之外的其他作用。在原发纤毛中发现了与关键信号通路相关的几种分子。这些包括声波刺猬,无翅,平面细胞极性和成纤维细胞生长因子,这对于许多细胞过程都是必不可少的。此外,“纤毛虫”基因的突变已在很大程度上显示出发育缺陷,例如体轴异常和脑畸形,这意味着纤毛相关的信号传导途径被破坏。因此,新出现的主题是初级纤毛可以充当信号转导的调节剂,以帮助在发育和体内平衡过程中在环境环境中塑造细胞反应。摘要:纤毛和信号通路之间的联系已成为理解纤毛病发病机制的框架。尽管睫状体生物学最近取得了进展,但是关于纤毛如何调节中枢神经系统中神经元功能的基本问题仍然存在。因此,对神经系统睫状功能的研究可能揭示神经发育过程中的纤毛调节机制,并提出疾病的新疗法。

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