Literature DB >> 26792399

Climbing fibers in spinocerebellar ataxia: A mechanism for the loss of motor control.

C J L M Smeets1, D S Verbeek2.   

Abstract

The spinocerebellar ataxias (SCAs) form an ever-growing group of neurodegenerative disorders causing dysfunction of the cerebellum and loss of motor control in patients. Currently, 41 different genetic causes have been identified, with each mutation affecting a different gene. Interestingly, these diverse genetic causes all disrupt cerebellar function and produce similar symptoms in patients. In order to understand the disease better, and define possible therapeutic targets for multiple SCAs, the field has been searching for common ground among the SCAs. In this review, we discuss the physiology of climbing fibers and the possibility that climbing fiber dysfunction is a point of convergence for at least a subset of SCAs.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Climbing fibers; Common pathology; Glutamate; Mouse models; Spinocerebellar ataxia; Synaptic plasticity

Mesh:

Year:  2016        PMID: 26792399     DOI: 10.1016/j.nbd.2016.01.009

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  17 in total

1.  Pharmacological induction of heat shock proteins ameliorates toxicity of mutant PKCγ in spinocerebellar ataxia type 14.

Authors:  Aoi Nakazono; Naoko Adachi; Hideyuki Takahashi; Takahiro Seki; Daizo Hamada; Takehiko Ueyama; Norio Sakai; Naoaki Saito
Journal:  J Biol Chem       Date:  2018-08-09       Impact factor: 5.157

2.  Postural Instability in Prodromal Spinocerebellar Ataxia Type 2: Insights into Cerebellar Involvement Before Onset of Permanent Ataxia.

Authors:  Luis Velázquez-Pérez; Gilberto Sánchez-Cruz; Roberto Rodríguez-Labrada; Mercedes Velázquez-Manresa; Ricardo Hechavarría-Pupo; Luis E Almaguer-Mederos
Journal:  Cerebellum       Date:  2017-02       Impact factor: 3.847

Review 3.  Dilemma of multiple system atrophy and spinocerebellar ataxias.

Authors:  Ming Li; Qianqian Ma; Xing Zhao; Can Wang; Huijie Wu; Jinyao Li; Wei Yang
Journal:  J Neurol       Date:  2018-04-26       Impact factor: 4.849

4.  A missense variant in ITPR1 provides evidence for autosomal recessive SCA29 with asymptomatic cerebellar hypoplasia in carriers.

Authors:  Joakim Klar; Zafar Ali; Muhammad Farooq; Kamal Khan; Johan Wikström; Maria Iqbal; Shumaila Zulfiqar; Sanam Faryal; Shahid Mahmood Baig; Niklas Dahl
Journal:  Eur J Hum Genet       Date:  2017-05-10       Impact factor: 4.246

5.  In Vivo Analysis of the Climbing Fiber-Purkinje Cell Circuit in SCA2-58Q Transgenic Mouse Model.

Authors:  Polina A Egorova; Alexandra V Gavrilova; Ilya B Bezprozvanny
Journal:  Cerebellum       Date:  2018-10       Impact factor: 3.847

Review 6.  Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2.

Authors:  Polina A Egorova; Ilya B Bezprozvanny
Journal:  Neurotherapeutics       Date:  2019-10       Impact factor: 7.620

7.  Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features.

Authors:  Zafar Ali; Shumaila Zulfiqar; Joakim Klar; Johan Wikström; Farid Ullah; Ayaz Khan; Uzma Abdullah; Shahid Baig; Niklas Dahl
Journal:  BMC Med Genet       Date:  2017-12-06       Impact factor: 2.103

Review 8.  Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches.

Authors:  Luis C Velázquez-Pérez; Roberto Rodríguez-Labrada; Juan Fernandez-Ruiz
Journal:  Front Neurol       Date:  2017-09-11       Impact factor: 4.003

Review 9.  Complex Spike Wars: a New Hope.

Authors:  Martha L Streng; Laurentiu S Popa; Timothy J Ebner
Journal:  Cerebellum       Date:  2018-12       Impact factor: 3.847

Review 10.  Purkinje Cell Signaling Deficits in Animal Models of Ataxia.

Authors:  Eriola Hoxha; Ilaria Balbo; Maria Concetta Miniaci; Filippo Tempia
Journal:  Front Synaptic Neurosci       Date:  2018-04-26
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