Kobayashi Yoshiki, Ito Kazuhiro, Kanda Akira, Tomoda Koich, Miller-Larsson Anna, Barnes Peter J, Mercado Nicolas
Airway Disease Section, National Heart and Lung Institute, Imperial College London, Guy Scadding Building, Royal Brompton Campus, Dovehouse Street, London, SW3 6LY, UK.
Airway Medicine, Department of Otolaryngology, Kansai Medical University, Osaka, Japan.
Respir Res. 2016 Mar 24;17:30. doi: 10.1186/s12931-016-0349-0.
We have recently reported that protein phosphate 2A (PP2A) inactivation resulted in increased phosphorylation of the mitogen-activated protein kinase (MAPK) c-Jun N-terminal kinase 1 (JNK1) and glucocorticoid receptors (GR) at Ser(226), thereby reducing GR nuclear translocation and causing corticosteroid insensitivity in severe asthmatics. Protein tyrosine phosphatases (PTPs) are also known to be critically involved in the regulation of MAPKs, such as JNK and therefore potentially associated with GR function. The aim of study was to elucidate the involvement of MAPK-PTPs (PTP-RR, PTP-N5 and PTP-N7), which can dephosphorylate MAPKs, in the regulation of corticosteroid sensitivity.
Corticosteroid sensitivity, GR nuclear translocation, phosphorylation levels of GR-Ser(226), JNK1 and PP2A catalytic subunit (PP2AC)-Tyr(307) and protein expression levels and activities of PTP-RR and PP2AC were evaluated in U937 cells and/or peripheral blood mononuclear cells (PBMCs). Knock-down effects of MAPK-PTPs using siRNA were also evaluated.
Knock-down of PTP-RR, but not of PTP-N5 or PTP-N7 impaired corticosteroid sensitivity, induced GR-Ser(226) phosphorylation and reduced GR nuclear translocation. Under IL-2/IL-4-induced corticosteroid insensitivity, PTP-RR expression, activity and associations with JNK1 and GR were reduced but PTP-RR activity was restored by formoterol. Also in PBMCs from severe asthmatic patients, PTP-RR and JNK1 expression were reduced and GR-Ser(226) phosphorylation increased. Furthermore, PTP-RR was associated with PP2A. PTP-RR reduction enhanced PP2AC-Tyr(307) phosphorylation leading to impairment of PP2A expression and activity.
We demonstrated that with corticosteroid insensitivity PTP-RR fails to reduce phosphorylation of JNK1 and GR-Ser(226), resulting in down-regulation of GR nuclear translocation. Reduced PTP-RR may represent a novel cause of corticosteroid insensitivity in severe asthmatics.
我们最近报道,蛋白磷酸酶2A(PP2A)失活导致丝裂原活化蛋白激酶(MAPK)c-Jun氨基末端激酶1(JNK1)和糖皮质激素受体(GR)在Ser(226)位点的磷酸化增加,从而减少GR的核转位,并导致重度哮喘患者出现糖皮质激素不敏感。蛋白酪氨酸磷酸酶(PTP)也被认为在JNK等MAPK的调节中起关键作用,因此可能与GR功能相关。本研究的目的是阐明可使MAPK去磷酸化的MAPK-PTP(PTP-RR、PTP-N5和PTP-N7)在糖皮质激素敏感性调节中的作用。
在U937细胞和/或外周血单核细胞(PBMC)中评估糖皮质激素敏感性、GR核转位、GR-Ser(226)、JNK1和PP2A催化亚基(PP2AC)-Tyr(307)的磷酸化水平以及PTP-RR和PP2AC的蛋白表达水平和活性。还评估了使用小干扰RNA(siRNA)对MAPK-PTP的敲低作用。
敲低PTP-RR而非PTP-N5或PTP-N7会损害糖皮质激素敏感性,诱导GR-Ser(226)磷酸化并减少GR核转位。在白细胞介素-2/白细胞介素-4诱导的糖皮质激素不敏感状态下,PTP-RR的表达、活性以及与JNK1和GR的结合减少,但福莫特罗可恢复PTP-RR的活性。同样,在重度哮喘患者的PBMC中,PTP-RR和JNK1的表达减少,GR-Ser(226)磷酸化增加。此外,PTP-RR与PP2A相关。PTP-RR减少会增强PP2AC-Tyr(307)磷酸化,导致PP2A的表达和活性受损。
我们证明,在糖皮质激素不敏感的情况下,PTP-RR无法降低JNK1和GR-Ser(226)的磷酸化,导致GR核转位下调。PTP-RR减少可能是重度哮喘患者糖皮质激素不敏感的一个新原因。