The role of primary cilia in neuronal function

被引:94
|
作者
Lee, Jeong Ho [1 ]
Gleeson, Joseph G. [1 ]
机构
[1] Univ Calif San Diego, Dept Neurosci & Pediat, Howard Hughes Med Inst, San Diego, CA 92103 USA
关键词
Ciliopathy; Joubert syndrome; Neuronal function; Primary cilia; BARDET-BIEDL-SYNDROME; INTRAFLAGELLAR TRANSPORT PROTEINS; POLYCYSTIC KIDNEY-DISEASE; JOUBERT-SYNDROME; SONIC HEDGEHOG; CENTROSOMAL PROTEIN; COUPLED-RECEPTORS; PROGENITOR POOL; CELL POLARITY; C-ELEGANS;
D O I
10.1016/j.nbd.2009.12.022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The "ciliopathies" are a newly defined group of disorders characterized by defects in the structure or function of the cellular primary cilium. Patients with these disorders display variably expressive fibrocystic renal disease, retinal blindness, polydactyly, obesity, and brain dysgenesis as well as neurocognitive impairments. Joubert syndrome is a ciliopathy defined by cerebellar vermis hypoplasia, oculomotor apraxia, intermittent hyperventilation, and mental retardation. Recent evidence suggests important roles for the primary cilium in mediating a host of extracellular signaling events such as morphogen, mitogen, homeostatic and polarity signals. Based upon the clinical features of ciliopathies and cilia mediated signaling pathways, the data support a role for the primary cilium in modulating neurogenesis, cell polarity, axonal guidance and possibly adult neuronal function. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:167 / 172
页数:6
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