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Gradient-dependent inhibition of stimulatory signaling from platelet G protein-coupled receptors
As platelet activation is an irreversible and potentially harmful event, platelet stimulatory signaling must be tightly regulated to ensure the filtering-out of inconsequential fluctuations of agonist concentrations in the vascular milieu. Herein, we show that platelet activation via G protein-coupl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ferrata Storti Foundation
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601095/ https://www.ncbi.nlm.nih.gov/pubmed/30630981 http://dx.doi.org/10.3324/haematol.2018.205815 |
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author | Macwan, Ankit S. Boknäs, Niklas Ntzouni, Maria P. Ramström, Sofia Gibbins, Jonathan M. Faxälv, Lars Lindahl, Tomas L. |
author_facet | Macwan, Ankit S. Boknäs, Niklas Ntzouni, Maria P. Ramström, Sofia Gibbins, Jonathan M. Faxälv, Lars Lindahl, Tomas L. |
author_sort | Macwan, Ankit S. |
collection | PubMed |
description | As platelet activation is an irreversible and potentially harmful event, platelet stimulatory signaling must be tightly regulated to ensure the filtering-out of inconsequential fluctuations of agonist concentrations in the vascular milieu. Herein, we show that platelet activation via G protein-coupled receptors is gradient-dependent, i.e., determined not only by agonist concentrations per se but also by how rapidly concentrations change over time. We demonstrate that gradient-dependent inhibition is a common feature of all major platelet stimulatory G protein-coupled receptors, while platelet activation via the non-G protein-coupled receptor glycoprotein VI is strictly concentration-dependent. By systematically characterizing the effects of variations in temporal agonist concentration gradients on different aspects of platelet activation, we demonstrate that gradient-dependent inhibition of protease-activated receptors exhibits different kinetics, with platelet activation occurring at lower agonist gradients for protease-activated receptor 4 than for protease-activated receptor 1, but shares a characteristic bimodal effect distribution, as gradient-dependent inhibition increases over a narrow range of gradients, below which aggregation and granule secretion is effectively shut off. In contrast, the effects of gradient-dependent inhibition on platelet activation via adenosine diphosphate and thromboxane receptors increase incrementally over a large range of gradients. Furthermore, depending on the affected activation pathway, gradient-dependent inhibition results in different degrees of refractoriness to subsequent autologous agonist stimulation. Mechanistically, our study identifies an important role for the cyclic adenosine monophosphate-dependent pathway in gradient-dependent inhibition. Together, our findings suggest that gradient-dependent inhibition may represent a new general mechanism for hemostatic regulation in platelets. |
format | Online Article Text |
id | pubmed-6601095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Ferrata Storti Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-66010952019-07-08 Gradient-dependent inhibition of stimulatory signaling from platelet G protein-coupled receptors Macwan, Ankit S. Boknäs, Niklas Ntzouni, Maria P. Ramström, Sofia Gibbins, Jonathan M. Faxälv, Lars Lindahl, Tomas L. Haematologica Article As platelet activation is an irreversible and potentially harmful event, platelet stimulatory signaling must be tightly regulated to ensure the filtering-out of inconsequential fluctuations of agonist concentrations in the vascular milieu. Herein, we show that platelet activation via G protein-coupled receptors is gradient-dependent, i.e., determined not only by agonist concentrations per se but also by how rapidly concentrations change over time. We demonstrate that gradient-dependent inhibition is a common feature of all major platelet stimulatory G protein-coupled receptors, while platelet activation via the non-G protein-coupled receptor glycoprotein VI is strictly concentration-dependent. By systematically characterizing the effects of variations in temporal agonist concentration gradients on different aspects of platelet activation, we demonstrate that gradient-dependent inhibition of protease-activated receptors exhibits different kinetics, with platelet activation occurring at lower agonist gradients for protease-activated receptor 4 than for protease-activated receptor 1, but shares a characteristic bimodal effect distribution, as gradient-dependent inhibition increases over a narrow range of gradients, below which aggregation and granule secretion is effectively shut off. In contrast, the effects of gradient-dependent inhibition on platelet activation via adenosine diphosphate and thromboxane receptors increase incrementally over a large range of gradients. Furthermore, depending on the affected activation pathway, gradient-dependent inhibition results in different degrees of refractoriness to subsequent autologous agonist stimulation. Mechanistically, our study identifies an important role for the cyclic adenosine monophosphate-dependent pathway in gradient-dependent inhibition. Together, our findings suggest that gradient-dependent inhibition may represent a new general mechanism for hemostatic regulation in platelets. Ferrata Storti Foundation 2019-07 /pmc/articles/PMC6601095/ /pubmed/30630981 http://dx.doi.org/10.3324/haematol.2018.205815 Text en Copyright© 2019 Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher. |
spellingShingle | Article Macwan, Ankit S. Boknäs, Niklas Ntzouni, Maria P. Ramström, Sofia Gibbins, Jonathan M. Faxälv, Lars Lindahl, Tomas L. Gradient-dependent inhibition of stimulatory signaling from platelet G protein-coupled receptors |
title | Gradient-dependent inhibition of stimulatory signaling from platelet G protein-coupled receptors |
title_full | Gradient-dependent inhibition of stimulatory signaling from platelet G protein-coupled receptors |
title_fullStr | Gradient-dependent inhibition of stimulatory signaling from platelet G protein-coupled receptors |
title_full_unstemmed | Gradient-dependent inhibition of stimulatory signaling from platelet G protein-coupled receptors |
title_short | Gradient-dependent inhibition of stimulatory signaling from platelet G protein-coupled receptors |
title_sort | gradient-dependent inhibition of stimulatory signaling from platelet g protein-coupled receptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601095/ https://www.ncbi.nlm.nih.gov/pubmed/30630981 http://dx.doi.org/10.3324/haematol.2018.205815 |
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