Cargando…
Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases
In addition to their canonical roles in translation the aminoacyl-tRNA synthetases (ARSs) have developed secondary functions over the course of evolution. Many of these activities are associated with cellular survival and nutritional stress responses essential for homeostatic processes in higher euk...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284789/ https://www.ncbi.nlm.nih.gov/pubmed/25535072 http://dx.doi.org/10.3390/ijms151223725 |
_version_ | 1782351464986836992 |
---|---|
author | Mirando, Adam C. Francklyn, Christopher S. Lounsbury, Karen M. |
author_facet | Mirando, Adam C. Francklyn, Christopher S. Lounsbury, Karen M. |
author_sort | Mirando, Adam C. |
collection | PubMed |
description | In addition to their canonical roles in translation the aminoacyl-tRNA synthetases (ARSs) have developed secondary functions over the course of evolution. Many of these activities are associated with cellular survival and nutritional stress responses essential for homeostatic processes in higher eukaryotes. In particular, six ARSs and one associated factor have documented functions in angiogenesis. However, despite their connection to this process, the ARSs are mechanistically distinct and exhibit a range of positive or negative effects on aspects of endothelial cell migration, proliferation, and survival. This variability is achieved through the appearance of appended domains and interplay with inflammatory pathways not found in prokaryotic systems. Complete knowledge of the non-canonical functions of ARSs is necessary to understand the mechanisms underlying the physiological regulation of angiogenesis. |
format | Online Article Text |
id | pubmed-4284789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-42847892015-01-21 Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases Mirando, Adam C. Francklyn, Christopher S. Lounsbury, Karen M. Int J Mol Sci Review In addition to their canonical roles in translation the aminoacyl-tRNA synthetases (ARSs) have developed secondary functions over the course of evolution. Many of these activities are associated with cellular survival and nutritional stress responses essential for homeostatic processes in higher eukaryotes. In particular, six ARSs and one associated factor have documented functions in angiogenesis. However, despite their connection to this process, the ARSs are mechanistically distinct and exhibit a range of positive or negative effects on aspects of endothelial cell migration, proliferation, and survival. This variability is achieved through the appearance of appended domains and interplay with inflammatory pathways not found in prokaryotic systems. Complete knowledge of the non-canonical functions of ARSs is necessary to understand the mechanisms underlying the physiological regulation of angiogenesis. MDPI 2014-12-19 /pmc/articles/PMC4284789/ /pubmed/25535072 http://dx.doi.org/10.3390/ijms151223725 Text en © 2014 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Mirando, Adam C. Francklyn, Christopher S. Lounsbury, Karen M. Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases |
title | Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases |
title_full | Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases |
title_fullStr | Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases |
title_full_unstemmed | Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases |
title_short | Regulation of Angiogenesis by Aminoacyl-tRNA Synthetases |
title_sort | regulation of angiogenesis by aminoacyl-trna synthetases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4284789/ https://www.ncbi.nlm.nih.gov/pubmed/25535072 http://dx.doi.org/10.3390/ijms151223725 |
work_keys_str_mv | AT mirandoadamc regulationofangiogenesisbyaminoacyltrnasynthetases AT francklynchristophers regulationofangiogenesisbyaminoacyltrnasynthetases AT lounsburykarenm regulationofangiogenesisbyaminoacyltrnasynthetases |