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神经纤毛发生的基础生物学和机制及 B9 家族。

Basic biology and mechanisms of neural ciliogenesis and the B9 family.

机构信息

Department of Biomedical Sciences and Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.

出版信息

Mol Neurobiol. 2012 Jun;45(3):564-70. doi: 10.1007/s12035-012-8276-7. Epub 2012 May 30.

Abstract

Although the discovery of cilia is one of the earliest in cell biology, the past two decades have witnessed an explosion of new insight into these enigmatic organelles. While long believed to be vestigial, cilia have recently moved into the spotlight as key players in multiple cellular processes, including brain development and homeostasis. This review focuses on the rapidly expanding basic biology of neural cilia, with special emphasis on the newly emerging B9 family of proteins. In particular, recent findings have identified a critical role for the B9 complex in a network of protein interactions that take place at the ciliary transition zone (TZ). We describe the essential role of these protein complexes in signaling cascades that require primary (nonmotile) cilia, including the sonic hedgehog pathway. Loss or dysfunction of ciliary trafficking and TZ function are linked to a number of neurologic diseases, which we propose to classify as neural ciliopathies. When taken together, the studies reviewed herein point to critical roles played by neural cilia, both in normal physiology and in disease.

摘要

尽管纤毛的发现是细胞生物学中最早的发现之一,但在过去的二十年中,人们对这些神秘细胞器的新认识如爆炸般涌现。尽管长期以来被认为是退化的,但纤毛最近成为了多个细胞过程的关键参与者,包括大脑发育和内稳态。本文重点介绍神经纤毛快速发展的基础生物学,特别强调新兴的 B9 蛋白家族。特别是,最近的发现确定了 B9 复合物在纤毛过渡区 (TZ) 发生的蛋白质相互作用网络中的关键作用。我们描述了这些蛋白复合物在信号级联反应中的重要作用,这些信号级联反应需要初级(非运动)纤毛,包括 sonic hedgehog 途径。纤毛运输和 TZ 功能的缺失或功能障碍与许多神经系统疾病有关,我们建议将这些疾病归类为神经纤毛病。综上所述,本文综述的研究表明,神经纤毛在正常生理和疾病中都发挥着关键作用。

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