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The Modulatory Roles of N-glycans in T-Cell-Mediated Autoimmune Diseases
Glycosylation is a ubiquitous posttranslational modification of proteins that occurs in the endoplasmic reticulum/Golgi. N-glycans and mucin-type O-glycans are achieved via a series of glycohydrolase- and glycosyltransferase-mediated reactions. Glycosylation modulates immune responses by regulating...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877641/ https://www.ncbi.nlm.nih.gov/pubmed/29518037 http://dx.doi.org/10.3390/ijms19030780 |
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author | Chien, Ming-Wei Fu, Shin-Huei Hsu, Chao-Yuan Liu, Yu-Wen Sytwu, Huey-Kang |
author_facet | Chien, Ming-Wei Fu, Shin-Huei Hsu, Chao-Yuan Liu, Yu-Wen Sytwu, Huey-Kang |
author_sort | Chien, Ming-Wei |
collection | PubMed |
description | Glycosylation is a ubiquitous posttranslational modification of proteins that occurs in the endoplasmic reticulum/Golgi. N-glycans and mucin-type O-glycans are achieved via a series of glycohydrolase- and glycosyltransferase-mediated reactions. Glycosylation modulates immune responses by regulating thymocyte development and T helper cell differentiation. Autoimmune diseases result from an abnormal immune response by self-antigens and subsequently lead to the destruction of the target tissues. The modification of N-glycans has been studied in several animal models of T-cell-mediated autoimmune diseases. This review summarizes and highlights the modulatory effects of N-glycosylation in several autoimmune diseases, including multiple sclerosis, systemic lupus erythematosus, inflammatory bowel disease, and type 1 diabetes mellitus. |
format | Online Article Text |
id | pubmed-5877641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58776412018-04-09 The Modulatory Roles of N-glycans in T-Cell-Mediated Autoimmune Diseases Chien, Ming-Wei Fu, Shin-Huei Hsu, Chao-Yuan Liu, Yu-Wen Sytwu, Huey-Kang Int J Mol Sci Review Glycosylation is a ubiquitous posttranslational modification of proteins that occurs in the endoplasmic reticulum/Golgi. N-glycans and mucin-type O-glycans are achieved via a series of glycohydrolase- and glycosyltransferase-mediated reactions. Glycosylation modulates immune responses by regulating thymocyte development and T helper cell differentiation. Autoimmune diseases result from an abnormal immune response by self-antigens and subsequently lead to the destruction of the target tissues. The modification of N-glycans has been studied in several animal models of T-cell-mediated autoimmune diseases. This review summarizes and highlights the modulatory effects of N-glycosylation in several autoimmune diseases, including multiple sclerosis, systemic lupus erythematosus, inflammatory bowel disease, and type 1 diabetes mellitus. MDPI 2018-03-08 /pmc/articles/PMC5877641/ /pubmed/29518037 http://dx.doi.org/10.3390/ijms19030780 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Chien, Ming-Wei Fu, Shin-Huei Hsu, Chao-Yuan Liu, Yu-Wen Sytwu, Huey-Kang The Modulatory Roles of N-glycans in T-Cell-Mediated Autoimmune Diseases |
title | The Modulatory Roles of N-glycans in T-Cell-Mediated Autoimmune Diseases |
title_full | The Modulatory Roles of N-glycans in T-Cell-Mediated Autoimmune Diseases |
title_fullStr | The Modulatory Roles of N-glycans in T-Cell-Mediated Autoimmune Diseases |
title_full_unstemmed | The Modulatory Roles of N-glycans in T-Cell-Mediated Autoimmune Diseases |
title_short | The Modulatory Roles of N-glycans in T-Cell-Mediated Autoimmune Diseases |
title_sort | modulatory roles of n-glycans in t-cell-mediated autoimmune diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877641/ https://www.ncbi.nlm.nih.gov/pubmed/29518037 http://dx.doi.org/10.3390/ijms19030780 |
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