Please use this identifier to cite or link to this item: https://doi.org/10.3390/ijms20030678
Title: Emerging regulatory roles of dual-specificity phosphatases in inflammatory airway disease
Authors: Manley, G.C.A. 
Parker, L.C.
Zhang, Y. 
Keywords: Asthma
COPD
Inflammation
Influenza
MAPK
Respiratory viruses
Rhinovirus
RSV
Issue Date: 2019
Publisher: MDPI AG
Citation: Manley, G.C.A., Parker, L.C., Zhang, Y. (2019). Emerging regulatory roles of dual-specificity phosphatases in inflammatory airway disease. International Journal of Molecular Sciences 20 (3) : 678. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms20030678
Rights: Attribution 4.0 International
Abstract: Inflammatory airway disease, such as asthma and chronic obstructive pulmonary disease (COPD), is a major health burden worldwide. These diseases cause large numbers of deaths each year due to airway obstruction, which is exacerbated by respiratory viral infection. The inflammatory response in the airway is mediated in part through the MAPK pathways: p38, JNK and ERK. These pathways also have roles in interferon production, viral replication, mucus production, and T cell responses, all of which are important processes in inflammatory airway disease. Dual-specificity phosphatases (DUSPs) are known to regulate the MAPKs, and roles for this family of proteins in the pathogenesis of airway disease are emerging. This review summarizes the function of DUSPs in regulation of cytokine expression, mucin production, and viral replication in the airway. The central role of DUSPs in T cell responses, including T cell activation, differentiation, and proliferation, will also be highlighted. In addition, the importance of this protein family in the lung, and the necessity of further investigation into their roles in airway disease, will be discussed. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.
Source Title: International Journal of Molecular Sciences
URI: https://scholarbank.nus.edu.sg/handle/10635/213728
ISSN: 16616596
DOI: 10.3390/ijms20030678
Rights: Attribution 4.0 International
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