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Integrin Activation States and Eosinophil Recruitment in Asthma

Eosinophil arrest and recruitment to the airway in asthma are mediated, at least in part, by integrins. Eosinophils express α(4)β(1), α(6)β(1), α(L)β(2), α(M)β(2), α(X)β(2), α(D)β(2), and α(4)β(7) integrins, which interact with counter-receptors on other cells or ligands in the extracellular matrix....

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Autores principales: Johansson, Mats W., Mosher, Deane F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3612688/
https://www.ncbi.nlm.nih.gov/pubmed/23554594
http://dx.doi.org/10.3389/fphar.2013.00033
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author Johansson, Mats W.
Mosher, Deane F.
author_facet Johansson, Mats W.
Mosher, Deane F.
author_sort Johansson, Mats W.
collection PubMed
description Eosinophil arrest and recruitment to the airway in asthma are mediated, at least in part, by integrins. Eosinophils express α(4)β(1), α(6)β(1), α(L)β(2), α(M)β(2), α(X)β(2), α(D)β(2), and α(4)β(7) integrins, which interact with counter-receptors on other cells or ligands in the extracellular matrix. Whether a given integrin-ligand pair mediates cell adhesion and migration depends on the activation state of the integrin. Integrins exist in an inactive bent, an intermediate-activity extended closed, and a high-activity extended open conformation. Integrin activation states can be monitored by conformation-specific monoclonal antibodies (mAbs). Studies in mice indicate that both β(1) and β(2) integrins mediate eosinophil recruitment to the lung. In vitro studies indicate that α(4)β(1) and α(M)β(2) are the principal integrins mediating eosinophil adhesion, including to vascular cell adhesion molecule-1 and the novel α(M)β(2) ligand periostin. In vivo, blood eosinophils have intermediate-activity β(1) integrins, as judged by mAb N29, apparently resulting from eosinophil binding of P-selectin on the surface of activated platelets, and have a proportion of their β(2) integrins in the intermediate conformation, as judged by mAb KIM-127, apparently due to exposure to low concentrations of interleukin-5 (IL-5). Airway eosinophils recovered by bronchoalveolar lavage (BAL) after segmental antigen challenge have high-activity β(1) integrins and high-activity α(M)β(2) that does not require IL-5. Here we review information on how the activation states of eosinophil β(1) and β(2) integrins correlate with measurements of eosinophil recruitment and pulmonary function in asthma. Blood eosinophil N29 reactivity is associated with decreased lung function under various circumstances in non-severe asthma and KIM-127 with BAL eosinophil numbers, indicating that intermediate-activity α(4)β(1) and α(M)β(2) of blood eosinophils are important for eosinophil arrest and consequently for recruitment and aspects of asthma.
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spelling pubmed-36126882013-04-01 Integrin Activation States and Eosinophil Recruitment in Asthma Johansson, Mats W. Mosher, Deane F. Front Pharmacol Pharmacology Eosinophil arrest and recruitment to the airway in asthma are mediated, at least in part, by integrins. Eosinophils express α(4)β(1), α(6)β(1), α(L)β(2), α(M)β(2), α(X)β(2), α(D)β(2), and α(4)β(7) integrins, which interact with counter-receptors on other cells or ligands in the extracellular matrix. Whether a given integrin-ligand pair mediates cell adhesion and migration depends on the activation state of the integrin. Integrins exist in an inactive bent, an intermediate-activity extended closed, and a high-activity extended open conformation. Integrin activation states can be monitored by conformation-specific monoclonal antibodies (mAbs). Studies in mice indicate that both β(1) and β(2) integrins mediate eosinophil recruitment to the lung. In vitro studies indicate that α(4)β(1) and α(M)β(2) are the principal integrins mediating eosinophil adhesion, including to vascular cell adhesion molecule-1 and the novel α(M)β(2) ligand periostin. In vivo, blood eosinophils have intermediate-activity β(1) integrins, as judged by mAb N29, apparently resulting from eosinophil binding of P-selectin on the surface of activated platelets, and have a proportion of their β(2) integrins in the intermediate conformation, as judged by mAb KIM-127, apparently due to exposure to low concentrations of interleukin-5 (IL-5). Airway eosinophils recovered by bronchoalveolar lavage (BAL) after segmental antigen challenge have high-activity β(1) integrins and high-activity α(M)β(2) that does not require IL-5. Here we review information on how the activation states of eosinophil β(1) and β(2) integrins correlate with measurements of eosinophil recruitment and pulmonary function in asthma. Blood eosinophil N29 reactivity is associated with decreased lung function under various circumstances in non-severe asthma and KIM-127 with BAL eosinophil numbers, indicating that intermediate-activity α(4)β(1) and α(M)β(2) of blood eosinophils are important for eosinophil arrest and consequently for recruitment and aspects of asthma. Frontiers Media S.A. 2013-04-01 /pmc/articles/PMC3612688/ /pubmed/23554594 http://dx.doi.org/10.3389/fphar.2013.00033 Text en Copyright © 2013 Johansson and Mosher. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Pharmacology
Johansson, Mats W.
Mosher, Deane F.
Integrin Activation States and Eosinophil Recruitment in Asthma
title Integrin Activation States and Eosinophil Recruitment in Asthma
title_full Integrin Activation States and Eosinophil Recruitment in Asthma
title_fullStr Integrin Activation States and Eosinophil Recruitment in Asthma
title_full_unstemmed Integrin Activation States and Eosinophil Recruitment in Asthma
title_short Integrin Activation States and Eosinophil Recruitment in Asthma
title_sort integrin activation states and eosinophil recruitment in asthma
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3612688/
https://www.ncbi.nlm.nih.gov/pubmed/23554594
http://dx.doi.org/10.3389/fphar.2013.00033
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