Role and regulation of MKP-1 in airway inflammation

被引:45
作者
Moosavi, Seyed M. [1 ,2 ]
Prabhala, Pavan [3 ,4 ,5 ]
Ammit, Alaina J. [1 ,2 ]
机构
[1] Univ Technol Sydney, Sch Life Sci, Sydney, NSW, Australia
[2] Univ Sydney, Woolcock Inst Med Res, Woolcock Emphysema Ctr, Sydney, NSW, Australia
[3] Univ Groningen, Dept Mol Pharmacol, Groningen, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Groningen Res Inst Asthma & COPD, Groningen, Netherlands
[5] Univ Groningen, Groningen Res Inst Pharm, Groningen, Netherlands
来源
RESPIRATORY RESEARCH | 2017年 / 18卷
基金
英国医学研究理事会;
关键词
ACTIVATED PROTEIN-KINASE; DUAL-SPECIFICITY PHOSPHATASE; IMMEDIATE-EARLY GENE; BETA(2)-ADRENOCEPTOR AGONISTS ENHANCE; OBSTRUCTIVE PULMONARY-DISEASE; SMOOTH-MUSCLE; MAPK-PHOSPHATASE; P38; MAPK; CORTICOSTEROID INSENSITIVITY; OXIDATIVE STRESS;
D O I
10.1186/s12931-017-0637-3
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Mitogen-activated protein kinase (MAPK) phosphatase 1 (MKP-1) is a protein with anti-inflammatory properties and the archetypal member of the dual-specificity phosphatases (DUSPs) family that have emerged over the past decade as playing an instrumental role in the regulation of airway inflammation. Not only does MKP-1 serve a critical role as a negative feedback effector, controlling the extent and duration of pro-inflammatory MAPK signalling in airway cells, upregulation of this endogenous phosphatase has also emerged as being one of the key cellular mechanism responsible for the beneficial actions of clinically-used respiratory medicines, including beta(2)-agonists, phosphodiesterase inhibitors and corticosteroids. Herein, we review the role and regulation of MKP-1 in the context of airway inflammation. We initially outline the structure and biochemistry of MKP-1 and summarise the multi-layered molecular mechanisms responsible for MKP-1 production more generally. We then focus in on some of the key in vitro studies in cell types relevant to airway disease that explain how MKP-1 can be regulated in airway inflammation at the transcriptional, post-translation and post-translational level. And finally, we address some of the potential challenges with MKP-1 upregulation that need to be explored further to fully exploit the potential of MKP-1 to repress airway inflammation in chronic respiratory disease.
引用
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页数:12
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