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Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics
Dysregulated expression and activity of cathepsin S (CTSS), a lysosomal protease and a member of the cysteine cathepsin protease family, is linked to the pathogenesis of multiple diseases, including a number of conditions affecting the lungs. Extracellular CTSS has potent elastase activity and by pr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216426/ https://www.ncbi.nlm.nih.gov/pubmed/32398133 http://dx.doi.org/10.1186/s12931-020-01381-5 |
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author | Brown, Ryan Nath, Sridesh Lora, Alnardo Samaha, Ghassan Elgamal, Ziyad Kaiser, Ryan Taggart, Clifford Weldon, Sinéad Geraghty, Patrick |
author_facet | Brown, Ryan Nath, Sridesh Lora, Alnardo Samaha, Ghassan Elgamal, Ziyad Kaiser, Ryan Taggart, Clifford Weldon, Sinéad Geraghty, Patrick |
author_sort | Brown, Ryan |
collection | PubMed |
description | Dysregulated expression and activity of cathepsin S (CTSS), a lysosomal protease and a member of the cysteine cathepsin protease family, is linked to the pathogenesis of multiple diseases, including a number of conditions affecting the lungs. Extracellular CTSS has potent elastase activity and by processing cytokines and host defense proteins, it also plays a role in the regulation of inflammation. CTSS has also been linked to G-coupled protein receptor activation and possesses an important intracellular role in major histocompatibility complex class II antigen presentation. Modulated CTSS activity is also associated with pulmonary disease comorbidities, such as cancer, cardiovascular disease, and diabetes. CTSS is expressed in a wide variety of immune cells and is biologically active at neutral pH. Herein, we review the significance of CTSS signaling in pulmonary diseases and associated comorbidities. We also discuss CTSS as a plausible therapeutic target and describe recent and current clinical trials examining CTSS inhibition as a means for treatment. |
format | Online Article Text |
id | pubmed-7216426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72164262020-05-18 Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics Brown, Ryan Nath, Sridesh Lora, Alnardo Samaha, Ghassan Elgamal, Ziyad Kaiser, Ryan Taggart, Clifford Weldon, Sinéad Geraghty, Patrick Respir Res Review Dysregulated expression and activity of cathepsin S (CTSS), a lysosomal protease and a member of the cysteine cathepsin protease family, is linked to the pathogenesis of multiple diseases, including a number of conditions affecting the lungs. Extracellular CTSS has potent elastase activity and by processing cytokines and host defense proteins, it also plays a role in the regulation of inflammation. CTSS has also been linked to G-coupled protein receptor activation and possesses an important intracellular role in major histocompatibility complex class II antigen presentation. Modulated CTSS activity is also associated with pulmonary disease comorbidities, such as cancer, cardiovascular disease, and diabetes. CTSS is expressed in a wide variety of immune cells and is biologically active at neutral pH. Herein, we review the significance of CTSS signaling in pulmonary diseases and associated comorbidities. We also discuss CTSS as a plausible therapeutic target and describe recent and current clinical trials examining CTSS inhibition as a means for treatment. BioMed Central 2020-05-12 2020 /pmc/articles/PMC7216426/ /pubmed/32398133 http://dx.doi.org/10.1186/s12931-020-01381-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Brown, Ryan Nath, Sridesh Lora, Alnardo Samaha, Ghassan Elgamal, Ziyad Kaiser, Ryan Taggart, Clifford Weldon, Sinéad Geraghty, Patrick Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics |
title | Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics |
title_full | Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics |
title_fullStr | Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics |
title_full_unstemmed | Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics |
title_short | Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics |
title_sort | cathepsin s: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216426/ https://www.ncbi.nlm.nih.gov/pubmed/32398133 http://dx.doi.org/10.1186/s12931-020-01381-5 |
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