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Gangliosides in nervous system development, regeneration, and pathologies
Gangliosides, sialic acid-containing sphingolipids, are major constituents of neuronal membranes. According to the number of sialic acids and the structure of the oligosaccharide chain, gangliosides can be classified as simple or complex and grouped in different ganglio-series. Hundreds of gangliosi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer - Medknow
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241395/ https://www.ncbi.nlm.nih.gov/pubmed/35799513 http://dx.doi.org/10.4103/1673-5374.343890 |
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author | Vasques, Juliana F. de Jesus Gonçalves, Renata Guedes da Silva-Junior, Almir Jordão Martins, Robertta Silva Gubert, Fernanda Mendez-Otero, Rosalia |
author_facet | Vasques, Juliana F. de Jesus Gonçalves, Renata Guedes da Silva-Junior, Almir Jordão Martins, Robertta Silva Gubert, Fernanda Mendez-Otero, Rosalia |
author_sort | Vasques, Juliana F. |
collection | PubMed |
description | Gangliosides, sialic acid-containing sphingolipids, are major constituents of neuronal membranes. According to the number of sialic acids and the structure of the oligosaccharide chain, gangliosides can be classified as simple or complex and grouped in different ganglio-series. Hundreds of gangliosides have been identified in vertebrate cells, with different expression patterns during development and related to several physiological processes, especially in the nervous system. While GD3 and its O-acetylated form, 9acGD3, are highly expressed in early developmental stages, GM1, GD1a, GD1b, and GT1b are the most abundant ganglioside species in the mature nervous system. Mutations in enzymes involved in ganglioside metabolism can lead to the accumulation of specific species, a condition termed gangliosidosis and usually marked by severe neurological impairment. Changes in ganglioside levels have also been described in several neurodegenerative diseases, such as Alzheimer’s and Parkinson’s. In this review, we summarized recent information about the roles of GD3, 9acGD3, GM1, GD1a, GD1b, GT1b, and other ganglioside species in nervous system development and regeneration, as well as clinical trials evaluating possible therapeutic applications of these molecules. |
format | Online Article Text |
id | pubmed-9241395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-92413952022-06-30 Gangliosides in nervous system development, regeneration, and pathologies Vasques, Juliana F. de Jesus Gonçalves, Renata Guedes da Silva-Junior, Almir Jordão Martins, Robertta Silva Gubert, Fernanda Mendez-Otero, Rosalia Neural Regen Res Review Gangliosides, sialic acid-containing sphingolipids, are major constituents of neuronal membranes. According to the number of sialic acids and the structure of the oligosaccharide chain, gangliosides can be classified as simple or complex and grouped in different ganglio-series. Hundreds of gangliosides have been identified in vertebrate cells, with different expression patterns during development and related to several physiological processes, especially in the nervous system. While GD3 and its O-acetylated form, 9acGD3, are highly expressed in early developmental stages, GM1, GD1a, GD1b, and GT1b are the most abundant ganglioside species in the mature nervous system. Mutations in enzymes involved in ganglioside metabolism can lead to the accumulation of specific species, a condition termed gangliosidosis and usually marked by severe neurological impairment. Changes in ganglioside levels have also been described in several neurodegenerative diseases, such as Alzheimer’s and Parkinson’s. In this review, we summarized recent information about the roles of GD3, 9acGD3, GM1, GD1a, GD1b, GT1b, and other ganglioside species in nervous system development and regeneration, as well as clinical trials evaluating possible therapeutic applications of these molecules. Wolters Kluwer - Medknow 2022-04-25 /pmc/articles/PMC9241395/ /pubmed/35799513 http://dx.doi.org/10.4103/1673-5374.343890 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Vasques, Juliana F. de Jesus Gonçalves, Renata Guedes da Silva-Junior, Almir Jordão Martins, Robertta Silva Gubert, Fernanda Mendez-Otero, Rosalia Gangliosides in nervous system development, regeneration, and pathologies |
title | Gangliosides in nervous system development, regeneration, and pathologies |
title_full | Gangliosides in nervous system development, regeneration, and pathologies |
title_fullStr | Gangliosides in nervous system development, regeneration, and pathologies |
title_full_unstemmed | Gangliosides in nervous system development, regeneration, and pathologies |
title_short | Gangliosides in nervous system development, regeneration, and pathologies |
title_sort | gangliosides in nervous system development, regeneration, and pathologies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241395/ https://www.ncbi.nlm.nih.gov/pubmed/35799513 http://dx.doi.org/10.4103/1673-5374.343890 |
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