scholarly journals mRNP assembly, axonal transport, and local translation in neurodegenerative diseases

2018 ◽  
Vol 1693 ◽  
pp. 75-91 ◽  
Author(s):  
Bilal Khalil ◽  
Dmytro Morderer ◽  
Phillip L. Price ◽  
Feilin Liu ◽  
Wilfried Rossoll
2021 ◽  
Vol 14 ◽  
Author(s):  
Seiichi Nagano ◽  
Toshiyuki Araki

Since neurons have long neurites including axons, it is crucial for the axons to transport many intracellular substances such as proteins and mitochondria in order to maintain their morphology and function. In addition, mRNAs have also been shown to be transported within axons. RNA-binding proteins form complexes with mRNAs, and regulate transport of the mRNAs to axons, as well as locally translate them into proteins. Local translation of mRNAs actively occurs during the development and damage of neurons, and plays an important role in axon elongation, regeneration, and synapse formation. In recent years, it has been reported that impaired axonal transport and local translation of mRNAs may be involved in the pathogenesis of some neurodegenerative diseases. In this review, we discuss the significance of mRNA axonal transport and their local translation in amyotrophic lateral sclerosis/frontotemporal dementia, spinal muscular atrophy, Alzheimer’s disease, and fragile X syndrome.


2000 ◽  
Vol 150 (1) ◽  
pp. 165-176 ◽  
Author(s):  
Steven Ackerley ◽  
Andrew J. Grierson ◽  
Janet Brownlees ◽  
Paul Thornhill ◽  
Brian H. Anderton ◽  
...  

Neurofilaments are transported through axons by slow axonal transport. Abnormal accumulations of neurofilaments are seen in several neurodegenerative diseases, and this suggests that neurofilament transport is defective. Excitotoxic mechanisms involving glutamate are believed to be part of the pathogenic process in some neurodegenerative diseases, but there is currently little evidence to link glutamate with neurofilament transport. We have used a novel technique involving transfection of the green fluorescent protein–tagged neurofilament middle chain to measure neurofilament transport in cultured neurons. Treatment of the cells with glutamate induces a slowing of neurofilament transport. Phosphorylation of the side-arm domains of neurofilaments has been associated with a slowing of neurofilament transport, and we show that glutamate causes increased phosphorylation of these domains in cell bodies. We also show that glutamate activates members of the mitogen-activated protein kinase family, and that these kinases will phosphorylate neurofilament side-arm domains. These results provide a molecular framework to link glutamate excitotoxicity with neurofilament accumulation seen in some neurodegenerative diseases.


2009 ◽  
pp. 1199-1203 ◽  
Author(s):  
S. Roy ◽  
V.M.-Y. Lee ◽  
J.Q. Trojanowski

PLoS ONE ◽  
2014 ◽  
Vol 9 (8) ◽  
pp. e104617 ◽  
Author(s):  
Min Jung Kang ◽  
Timothy J. Hansen ◽  
Monique Mickiewicz ◽  
Tadeusz J. Kaczynski ◽  
Samantha Fye ◽  
...  

2009 ◽  
Vol 29 (41) ◽  
pp. 12776-12786 ◽  
Author(s):  
G. A. Morfini ◽  
M. Burns ◽  
L. I. Binder ◽  
N. M. Kanaan ◽  
N. LaPointe ◽  
...  

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