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GDNF synthesis, signaling, and retrograde transport in motor neurons

Glial cell line–derived neurotrophic factor (GDNF) is a 134 amino acid protein belonging in the GDNF family ligands (GFLs). GDNF was originally isolated from rat glial cell lines and identified as a neurotrophic factor with the ability to promote dopamine uptake within midbrain dopaminergic neurons....

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Autores principales: Cintrón-Colón, Alberto F., Almeida-Alves, Gabriel, Boynton, Alicia M., Spitsbergen, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529617/
https://www.ncbi.nlm.nih.gov/pubmed/32897420
http://dx.doi.org/10.1007/s00441-020-03287-6
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author Cintrón-Colón, Alberto F.
Almeida-Alves, Gabriel
Boynton, Alicia M.
Spitsbergen, John M.
author_facet Cintrón-Colón, Alberto F.
Almeida-Alves, Gabriel
Boynton, Alicia M.
Spitsbergen, John M.
author_sort Cintrón-Colón, Alberto F.
collection PubMed
description Glial cell line–derived neurotrophic factor (GDNF) is a 134 amino acid protein belonging in the GDNF family ligands (GFLs). GDNF was originally isolated from rat glial cell lines and identified as a neurotrophic factor with the ability to promote dopamine uptake within midbrain dopaminergic neurons. Since its discovery, the potential neuroprotective effects of GDNF have been researched extensively, and the effect of GDNF on motor neurons will be discussed herein. Similar to other members of the TGF-β superfamily, GDNF is first synthesized as a precursor protein (pro-GDNF). After a series of protein cleavage and processing, the 211 amino acid pro-GDNF is finally converted into the active and mature form of GDNF. GDNF has the ability to trigger receptor tyrosine kinase RET phosphorylation, whose downstream effects have been found to promote neuronal health and survival. The binding of GDNF to its receptors triggers several intracellular signaling pathways which play roles in promoting the development, survival, and maintenance of neuron-neuron and neuron-target tissue interactions. The synthesis and regulation of GDNF have been shown to be altered in many diseases, aging, exercise, and addiction. The neuroprotective effects of GDNF may be used to develop treatments and therapies to ameliorate neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS). In this review, we provide a detailed discussion of the general roles of GDNF and its production, delivery, secretion, and neuroprotective effects on motor neurons within the mammalian neuromuscular system.
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spelling pubmed-75296172020-10-19 GDNF synthesis, signaling, and retrograde transport in motor neurons Cintrón-Colón, Alberto F. Almeida-Alves, Gabriel Boynton, Alicia M. Spitsbergen, John M. Cell Tissue Res Review Glial cell line–derived neurotrophic factor (GDNF) is a 134 amino acid protein belonging in the GDNF family ligands (GFLs). GDNF was originally isolated from rat glial cell lines and identified as a neurotrophic factor with the ability to promote dopamine uptake within midbrain dopaminergic neurons. Since its discovery, the potential neuroprotective effects of GDNF have been researched extensively, and the effect of GDNF on motor neurons will be discussed herein. Similar to other members of the TGF-β superfamily, GDNF is first synthesized as a precursor protein (pro-GDNF). After a series of protein cleavage and processing, the 211 amino acid pro-GDNF is finally converted into the active and mature form of GDNF. GDNF has the ability to trigger receptor tyrosine kinase RET phosphorylation, whose downstream effects have been found to promote neuronal health and survival. The binding of GDNF to its receptors triggers several intracellular signaling pathways which play roles in promoting the development, survival, and maintenance of neuron-neuron and neuron-target tissue interactions. The synthesis and regulation of GDNF have been shown to be altered in many diseases, aging, exercise, and addiction. The neuroprotective effects of GDNF may be used to develop treatments and therapies to ameliorate neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS). In this review, we provide a detailed discussion of the general roles of GDNF and its production, delivery, secretion, and neuroprotective effects on motor neurons within the mammalian neuromuscular system. Springer Berlin Heidelberg 2020-09-08 2020 /pmc/articles/PMC7529617/ /pubmed/32897420 http://dx.doi.org/10.1007/s00441-020-03287-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Cintrón-Colón, Alberto F.
Almeida-Alves, Gabriel
Boynton, Alicia M.
Spitsbergen, John M.
GDNF synthesis, signaling, and retrograde transport in motor neurons
title GDNF synthesis, signaling, and retrograde transport in motor neurons
title_full GDNF synthesis, signaling, and retrograde transport in motor neurons
title_fullStr GDNF synthesis, signaling, and retrograde transport in motor neurons
title_full_unstemmed GDNF synthesis, signaling, and retrograde transport in motor neurons
title_short GDNF synthesis, signaling, and retrograde transport in motor neurons
title_sort gdnf synthesis, signaling, and retrograde transport in motor neurons
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529617/
https://www.ncbi.nlm.nih.gov/pubmed/32897420
http://dx.doi.org/10.1007/s00441-020-03287-6
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