Cathepsin S: investigating an old player in lung disease pathogenesis, comorbidities, and potential therapeutics.


Journal

Respiratory research
ISSN: 1465-993X
Titre abrégé: Respir Res
Pays: England
ID NLM: 101090633

Informations de publication

Date de publication:
12 May 2020
Historique:
received: 03 03 2020
accepted: 01 05 2020
entrez: 14 5 2020
pubmed: 14 5 2020
medline: 13 3 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 32398133
doi: 10.1186/s12931-020-01381-5
pii: 10.1186/s12931-020-01381-5
pmc: PMC7216426
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Inflammation Mediators 0
Cathepsins EC 3.4.-
cathepsin S EC 3.4.22.27

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

111

Subventions

Organisme : Alpha-1 Foundation
ID : 614218
Organisme : Medical Research Council
ID : MR/P022847/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_13075
Pays : United Kingdom
Organisme : Rosetrees Trust
ID : A2450
Organisme : Cystic Fibrosis Foundation
ID : WELDON18G0
Organisme : Flight Attendant Medical Research Institute
ID : CIA160005

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Auteurs

Ryan Brown (R)

Airway Innate Immunity Research (AiiR) Group, Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, Northern Ireland, UK.

Sridesh Nath (S)

Division of Pulmonary & Critical Care Medicine, Department of Medicine, State University of New York Downstate Medical Centre, Brooklyn, NY, USA.

Alnardo Lora (A)

Division of Pulmonary & Critical Care Medicine, Department of Medicine, State University of New York Downstate Medical Centre, Brooklyn, NY, USA.

Ghassan Samaha (G)

Division of Pulmonary & Critical Care Medicine, Department of Medicine, State University of New York Downstate Medical Centre, Brooklyn, NY, USA.

Ziyad Elgamal (Z)

Division of Pulmonary & Critical Care Medicine, Department of Medicine, State University of New York Downstate Medical Centre, Brooklyn, NY, USA.

Ryan Kaiser (R)

Division of Pulmonary & Critical Care Medicine, Department of Medicine, State University of New York Downstate Medical Centre, Brooklyn, NY, USA.

Clifford Taggart (C)

Airway Innate Immunity Research (AiiR) Group, Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, Northern Ireland, UK.

Sinéad Weldon (S)

Airway Innate Immunity Research (AiiR) Group, Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, Northern Ireland, UK.

Patrick Geraghty (P)

Division of Pulmonary & Critical Care Medicine, Department of Medicine, State University of New York Downstate Medical Centre, Brooklyn, NY, USA. Patrick.Geraghty@downstate.edu.
Department of Cell Biology, State University of New York Downstate Medical Centre, Brooklyn, NY, USA. Patrick.Geraghty@downstate.edu.

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