Cargando…
Secreted Threonyl-tRNA synthetase stimulates endothelial cell migration and angiogenesis
Aminoacyl-tRNA synthetases classically regulate protein synthesis but some also engage in alternative signaling functions related to immune responses and angiogenesis. Threonyl-tRNA synthetase (TARS) is an autoantigen in the autoimmune disorder myositis, and borrelidin, a potent inhibitor of TARS, i...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578223/ https://www.ncbi.nlm.nih.gov/pubmed/23425968 http://dx.doi.org/10.1038/srep01317 |
_version_ | 1782260011784732672 |
---|---|
author | Williams, Tamara F. Mirando, Adam C. Wilkinson, Barrie Francklyn, Christopher S. Lounsbury, Karen M. |
author_facet | Williams, Tamara F. Mirando, Adam C. Wilkinson, Barrie Francklyn, Christopher S. Lounsbury, Karen M. |
author_sort | Williams, Tamara F. |
collection | PubMed |
description | Aminoacyl-tRNA synthetases classically regulate protein synthesis but some also engage in alternative signaling functions related to immune responses and angiogenesis. Threonyl-tRNA synthetase (TARS) is an autoantigen in the autoimmune disorder myositis, and borrelidin, a potent inhibitor of TARS, inhibits angiogenesis. We explored a mechanistic link between these findings by testing whether TARS directly affects angiogenesis through inflammatory mediators. When human vascular endothelial cells were exposed to tumor necrosis factor-α (TNF-α) or vascular endothelial growth factor (VEGF), TARS was secreted into the cell media. Furthermore, exogenous TARS stimulated endothelial cell migration and angiogenesis in both in vitro and in vivo assays. The borrelidin derivative BC194 reduced the angiogenic effect of both VEGF and TARS, but not a borrelidin-resistant TARS mutant. Our findings reveal a previously undiscovered function for TARS as an angiogenic, pro-migratory extracellular signaling molecule. TARS thus provides a potential target for detecting or interdicting disease-related inflammatory or angiogenic responses. |
format | Online Article Text |
id | pubmed-3578223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-35782232013-02-21 Secreted Threonyl-tRNA synthetase stimulates endothelial cell migration and angiogenesis Williams, Tamara F. Mirando, Adam C. Wilkinson, Barrie Francklyn, Christopher S. Lounsbury, Karen M. Sci Rep Article Aminoacyl-tRNA synthetases classically regulate protein synthesis but some also engage in alternative signaling functions related to immune responses and angiogenesis. Threonyl-tRNA synthetase (TARS) is an autoantigen in the autoimmune disorder myositis, and borrelidin, a potent inhibitor of TARS, inhibits angiogenesis. We explored a mechanistic link between these findings by testing whether TARS directly affects angiogenesis through inflammatory mediators. When human vascular endothelial cells were exposed to tumor necrosis factor-α (TNF-α) or vascular endothelial growth factor (VEGF), TARS was secreted into the cell media. Furthermore, exogenous TARS stimulated endothelial cell migration and angiogenesis in both in vitro and in vivo assays. The borrelidin derivative BC194 reduced the angiogenic effect of both VEGF and TARS, but not a borrelidin-resistant TARS mutant. Our findings reveal a previously undiscovered function for TARS as an angiogenic, pro-migratory extracellular signaling molecule. TARS thus provides a potential target for detecting or interdicting disease-related inflammatory or angiogenic responses. Nature Publishing Group 2013-02-21 /pmc/articles/PMC3578223/ /pubmed/23425968 http://dx.doi.org/10.1038/srep01317 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Williams, Tamara F. Mirando, Adam C. Wilkinson, Barrie Francklyn, Christopher S. Lounsbury, Karen M. Secreted Threonyl-tRNA synthetase stimulates endothelial cell migration and angiogenesis |
title | Secreted Threonyl-tRNA synthetase stimulates endothelial cell migration and angiogenesis |
title_full | Secreted Threonyl-tRNA synthetase stimulates endothelial cell migration and angiogenesis |
title_fullStr | Secreted Threonyl-tRNA synthetase stimulates endothelial cell migration and angiogenesis |
title_full_unstemmed | Secreted Threonyl-tRNA synthetase stimulates endothelial cell migration and angiogenesis |
title_short | Secreted Threonyl-tRNA synthetase stimulates endothelial cell migration and angiogenesis |
title_sort | secreted threonyl-trna synthetase stimulates endothelial cell migration and angiogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578223/ https://www.ncbi.nlm.nih.gov/pubmed/23425968 http://dx.doi.org/10.1038/srep01317 |
work_keys_str_mv | AT williamstamaraf secretedthreonyltrnasynthetasestimulatesendothelialcellmigrationandangiogenesis AT mirandoadamc secretedthreonyltrnasynthetasestimulatesendothelialcellmigrationandangiogenesis AT wilkinsonbarrie secretedthreonyltrnasynthetasestimulatesendothelialcellmigrationandangiogenesis AT francklynchristophers secretedthreonyltrnasynthetasestimulatesendothelialcellmigrationandangiogenesis AT lounsburykarenm secretedthreonyltrnasynthetasestimulatesendothelialcellmigrationandangiogenesis |