Literature DB >> 21386674

Cilia in the nervous system: linking cilia function and neurodevelopmental disorders.

Ji E Lee1, Joseph G Gleeson.   

Abstract

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.

Entities:  

Mesh:

Year:  2011        PMID: 21386674      PMCID: PMC3984876          DOI: 10.1097/WCO.0b013e3283444d05

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  65 in total

Review 1.  Polyglutamylation and the fleer gene.

Authors:  Narendra H Pathak; Iain A Drummond
Journal:  Methods Cell Biol       Date:  2009-12-23       Impact factor: 1.441

Review 2.  Clinical and molecular features of Joubert syndrome and related disorders.

Authors:  Melissa A Parisi
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

Review 3.  The ependyma: a protective barrier between brain and cerebrospinal fluid.

Authors:  M R Del Bigio
Journal:  Glia       Date:  1995-05       Impact factor: 7.452

4.  Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus.

Authors:  Boglarka Banizs; Martin M Pike; C Leigh Millican; William B Ferguson; Peter Komlosi; James Sheetz; Phillip D Bell; Erik M Schwiebert; Bradley K Yoder
Journal:  Development       Date:  2005-12       Impact factor: 6.868

5.  Tubulin glutamylation regulates ciliary motility by altering inner dynein arm activity.

Authors:  Swati Suryavanshi; Bernard Eddé; Laura A Fox; Stella Guerrero; Robert Hard; Todd Hennessey; Amrita Kabi; David Malison; David Pennock; Winfield S Sale; Dorota Wloga; Jacek Gaertig
Journal:  Curr Biol       Date:  2010-03-09       Impact factor: 10.834

6.  Tubulin polyglutamylation is essential for airway ciliary function through the regulation of beating asymmetry.

Authors:  Koji Ikegami; Showbu Sato; Kenji Nakamura; Lawrence E Ostrowski; Mitsutoshi Setou
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-24       Impact factor: 11.205

Review 7.  Cerebellar and brainstem development: an overview in relation to Joubert syndrome.

Authors:  A T Yachnis; L B Rorke
Journal:  J Child Neurol       Date:  1999-09       Impact factor: 1.987

8.  DISC1 regulates primary cilia that display specific dopamine receptors.

Authors:  Aaron Marley; Mark von Zastrow
Journal:  PLoS One       Date:  2010-05-28       Impact factor: 3.240

9.  Ttc21b is required to restrict sonic hedgehog activity in the developing mouse forebrain.

Authors:  R W Stottmann; P V Tran; A Turbe-Doan; D R Beier
Journal:  Dev Biol       Date:  2009-09-02       Impact factor: 3.582

10.  Bardet-biedl syndrome and brain abnormalities.

Authors:  C Rooryck; S Pelras; J-F Chateil; C Cances; B Arveiler; A Verloes; D Lacombe; C Goizet
Journal:  Neuropediatrics       Date:  2007-02       Impact factor: 1.947

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  81 in total

Review 1.  Axonemal positioning and orientation in three-dimensional space for primary cilia: what is known, what is assumed, and what needs clarification.

Authors:  Cornelia E Farnum; Norman J Wilsman
Journal:  Dev Dyn       Date:  2011-11       Impact factor: 3.780

Review 2.  Primary cilia and coordination of receptor tyrosine kinase (RTK) signalling.

Authors:  Søren T Christensen; Christian A Clement; Peter Satir; Lotte B Pedersen
Journal:  J Pathol       Date:  2011-11-21       Impact factor: 7.996

3.  Neuronal primary cilia: an underappreciated signaling and sensory organelle in the brain.

Authors:  Jill A Green; Kirk Mykytyn
Journal:  Neuropsychopharmacology       Date:  2014-01       Impact factor: 7.853

Review 4.  Integrative mechanisms of oriented neuronal migration in the developing brain.

Authors:  Irina Evsyukova; Charlotte Plestant; E S Anton
Journal:  Annu Rev Cell Dev Biol       Date:  2013-08-07       Impact factor: 13.827

5.  The XLID protein PQBP1 and the GTPase Dynamin 2 define a signaling link that orchestrates ciliary morphogenesis in postmitotic neurons.

Authors:  Yoshiho Ikeuchi; Luis de la Torre-Ubieta; Takahiko Matsuda; Hanno Steen; Hitoshi Okazawa; Azad Bonni
Journal:  Cell Rep       Date:  2013-08-29       Impact factor: 9.423

6.  The Chlamydomonas mutant pf27 reveals novel features of ciliary radial spoke assembly.

Authors:  Lea M Alford; Alexa L Mattheyses; Emily L Hunter; Huawen Lin; Susan K Dutcher; Winfield S Sale
Journal:  Cytoskeleton (Hoboken)       Date:  2013-12

7.  Ultrastructural changes in the progress of natural Scrapie regardless fixation protocol.

Authors:  Rocío Sarasa; Concepción Junquera; Adolfo Toledano; Juan José Badiola; Marta Monzón
Journal:  Histochem Cell Biol       Date:  2015-02-28       Impact factor: 4.304

8.  Brain Dysplasia Associated with Ciliary Dysfunction in Infants with Congenital Heart Disease.

Authors:  Ashok Panigrahy; Vincent Lee; Rafael Ceschin; Giulio Zuccoli; Nancy Beluk; Omar Khalifa; Jodie K Votava-Smith; Mark DeBrunner; Ricardo Munoz; Yuliya Domnina; Victor Morell; Peter Wearden; Joan Sanchez De Toledo; William Devine; Maliha Zahid; Cecilia W Lo
Journal:  J Pediatr       Date:  2016-08-26       Impact factor: 4.406

Review 9.  Using C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disorders.

Authors:  Carlos Bessa; Patrícia Maciel; Ana João Rodrigues
Journal:  Mol Neurobiol       Date:  2013-03-14       Impact factor: 5.590

10.  Disruption of polycystin-L causes hippocampal and thalamocortical hyperexcitability.

Authors:  Gang Yao; Chong Luo; Michael Harvey; Maoqing Wu; Taylor H Schreiber; Yanjun Du; Nuria Basora; Xuefeng Su; Diego Contreras; Jing Zhou
Journal:  Hum Mol Genet       Date:  2015-11-26       Impact factor: 6.150

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