The expression and activity of cathepsins D, H and K in asthmatic airways.

Tumstatin is an anti-angiogenic collagen IV α3 fragment, levels of which are reduced in the airways of asthmatics. Its reduction may be due to the degradation by extracellular matrix (ECM) proteases. Cathepsins play a role in ECM remodelling, with cathepsin D, H and K (CTSD, CTSH and CTSK) being ass...

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Main Authors: Alen Faiz, Gavin Tjin, Louise Harkness, Markus Weckmann, Shisan Bao, Judith L Black, Brian G G Oliver, Janette K Burgess
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3590183?pdf=render
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spelling doaj-773520963db848a391ec73e7b1113f902020-11-24T21:12:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5724510.1371/journal.pone.0057245The expression and activity of cathepsins D, H and K in asthmatic airways.Alen FaizGavin TjinLouise HarknessMarkus WeckmannShisan BaoJudith L BlackBrian G G OliverJanette K BurgessTumstatin is an anti-angiogenic collagen IV α3 fragment, levels of which are reduced in the airways of asthmatics. Its reduction may be due to the degradation by extracellular matrix (ECM) proteases. Cathepsins play a role in ECM remodelling, with cathepsin D, H and K (CTSD, CTSH and CTSK) being associated with lung diseases. CTSD modulates the NC1 domains of collagen molecules including tumstatin, while CTSH and CTSK are involved in ECM degradation. The role of these cathepsins in the regulation of tumstatin in the lung has not previously been examined. We demonstrated that CTSB, D, F, H, K, L and S mRNA was expressed in the airways. Quantification of immunohistochemistry showed that there is no difference in the global expression of CTSD, CTSH and CTSK between asthmatics and non-asthmatics. CTSD and CTSK, but not CTSH had the capacity to degrade tumstatin. No difference was observed in the activity of CTSD and H in bronchoalveolar lavage fluid of asthmatic and non-asthmatics, while CTSK was undetectable. This indicates that while CTSD possesses the potential to directly regulate tumstatin, and thus angiogenesis through this mechanism however, it is not likely to be involved in the dysregulation of tumstatin found in asthmatic airways.http://europepmc.org/articles/PMC3590183?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Alen Faiz
Gavin Tjin
Louise Harkness
Markus Weckmann
Shisan Bao
Judith L Black
Brian G G Oliver
Janette K Burgess
spellingShingle Alen Faiz
Gavin Tjin
Louise Harkness
Markus Weckmann
Shisan Bao
Judith L Black
Brian G G Oliver
Janette K Burgess
The expression and activity of cathepsins D, H and K in asthmatic airways.
PLoS ONE
author_facet Alen Faiz
Gavin Tjin
Louise Harkness
Markus Weckmann
Shisan Bao
Judith L Black
Brian G G Oliver
Janette K Burgess
author_sort Alen Faiz
title The expression and activity of cathepsins D, H and K in asthmatic airways.
title_short The expression and activity of cathepsins D, H and K in asthmatic airways.
title_full The expression and activity of cathepsins D, H and K in asthmatic airways.
title_fullStr The expression and activity of cathepsins D, H and K in asthmatic airways.
title_full_unstemmed The expression and activity of cathepsins D, H and K in asthmatic airways.
title_sort expression and activity of cathepsins d, h and k in asthmatic airways.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Tumstatin is an anti-angiogenic collagen IV α3 fragment, levels of which are reduced in the airways of asthmatics. Its reduction may be due to the degradation by extracellular matrix (ECM) proteases. Cathepsins play a role in ECM remodelling, with cathepsin D, H and K (CTSD, CTSH and CTSK) being associated with lung diseases. CTSD modulates the NC1 domains of collagen molecules including tumstatin, while CTSH and CTSK are involved in ECM degradation. The role of these cathepsins in the regulation of tumstatin in the lung has not previously been examined. We demonstrated that CTSB, D, F, H, K, L and S mRNA was expressed in the airways. Quantification of immunohistochemistry showed that there is no difference in the global expression of CTSD, CTSH and CTSK between asthmatics and non-asthmatics. CTSD and CTSK, but not CTSH had the capacity to degrade tumstatin. No difference was observed in the activity of CTSD and H in bronchoalveolar lavage fluid of asthmatic and non-asthmatics, while CTSK was undetectable. This indicates that while CTSD possesses the potential to directly regulate tumstatin, and thus angiogenesis through this mechanism however, it is not likely to be involved in the dysregulation of tumstatin found in asthmatic airways.
url http://europepmc.org/articles/PMC3590183?pdf=render
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