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Progress and challenge of microRNA research in immunity
MicroRNAs (miRNAs) are 19–24 nucleotide long non-coding RNA species that regulate the expression of multiple target genes at the post-transcriptional level. They are required for normal immune system development and function, and their expression is dynamically regulated in different immune cell sub...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053854/ https://www.ncbi.nlm.nih.gov/pubmed/24971086 http://dx.doi.org/10.3389/fgene.2014.00178 |
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author | Lee, Hyang-Mi Nguyen, Duc T. Lu, Li-Fan |
author_facet | Lee, Hyang-Mi Nguyen, Duc T. Lu, Li-Fan |
author_sort | Lee, Hyang-Mi |
collection | PubMed |
description | MicroRNAs (miRNAs) are 19–24 nucleotide long non-coding RNA species that regulate the expression of multiple target genes at the post-transcriptional level. They are required for normal immune system development and function, and their expression is dynamically regulated in different immune cell subsets during lineage differentiation and immune response. Aberrant expression of miRNAs results in dysregulated innate and adaptive immunity. This in turn can lead to failure to fight against invading pathogens and the development of autoimmune diseases and hematopoietic malignancies. In this article, we review current progress in miRNA research in immunity in both physiological and pathological settings. We also discuss research limitations and challenges that researchers are just beginning to solve. |
format | Online Article Text |
id | pubmed-4053854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40538542014-06-26 Progress and challenge of microRNA research in immunity Lee, Hyang-Mi Nguyen, Duc T. Lu, Li-Fan Front Genet Genetics MicroRNAs (miRNAs) are 19–24 nucleotide long non-coding RNA species that regulate the expression of multiple target genes at the post-transcriptional level. They are required for normal immune system development and function, and their expression is dynamically regulated in different immune cell subsets during lineage differentiation and immune response. Aberrant expression of miRNAs results in dysregulated innate and adaptive immunity. This in turn can lead to failure to fight against invading pathogens and the development of autoimmune diseases and hematopoietic malignancies. In this article, we review current progress in miRNA research in immunity in both physiological and pathological settings. We also discuss research limitations and challenges that researchers are just beginning to solve. Frontiers Media S.A. 2014-06-12 /pmc/articles/PMC4053854/ /pubmed/24971086 http://dx.doi.org/10.3389/fgene.2014.00178 Text en Copyright © 2014 Lee, Nguyen and Lu. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Lee, Hyang-Mi Nguyen, Duc T. Lu, Li-Fan Progress and challenge of microRNA research in immunity |
title | Progress and challenge of microRNA research in immunity |
title_full | Progress and challenge of microRNA research in immunity |
title_fullStr | Progress and challenge of microRNA research in immunity |
title_full_unstemmed | Progress and challenge of microRNA research in immunity |
title_short | Progress and challenge of microRNA research in immunity |
title_sort | progress and challenge of microrna research in immunity |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053854/ https://www.ncbi.nlm.nih.gov/pubmed/24971086 http://dx.doi.org/10.3389/fgene.2014.00178 |
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