β-arrestin2 stimulates interleukin-17 production and expression of cd4+ t lymphocytes in a murine asthma model

نویسندگان

yi liu department of respiratory medicine, the second xiangya hospital of central south university, changsha, hunan 410011, china

gu-yi wang department of respiratory medicine, the second xiangya hospital of central south university, changsha, hunan 410011, china

shao-kun liu department of respiratory medicine, the second xiangya hospital of central south university, changsha, hunan 410011, china

mu-yi yang department of respiratory medicine, the second xiangya hospital of central south university, changsha, hunan 410011, china

چکیده

allergic asthma is a complex and chronic inflammatory airway disease. interleukin-17 is a pro-inflammatory cytokine which plays critical role in the pathogenesis of allergic asthma. it has been reported that β-arrestin2 regulated the development of allergic asthma at a proximal step in the inflammatory cascade. in this study, the influence of β-arrestin2 on interleukin-17 production and expression of cd4+  t lymphocytes in a murine asthma model was investigated. splenic cd4+   t lymphocytes from  wild-type mice and those  from  a murine asthma model were purified. cd4+  t lymphocytes from a murine asthma model were transfected with  sirnas  targeting the  β-arrestin2  or  were pretreated  with  the  erk1/2  inhibitor,pd98059.  after  stimulation,  the   protein   expression  of   β-arrestin2、phosphorylated- erk1/2 and il-17 were detection by western blot; the mrna expression of il-17 were detected by real-time pcr; the accumulation of il-17 in supernatants  were detected by elisa. we found that β-arrestin2、phosphorylated-erk1/2 and il-17 expression in cd4+  t lymphocytes from a murine asthma model was increased compared with those from wild- type mice(p<0.01). treatment of cd4+  t lymphocytes with sirnas targeting the β-arrestin2 down-regulated phosphorylated-  erk  1/2  and  il-17 expression  (p <  0.01). pd98059 decreased il-17 production  and expression in cd4+   t lymphocytes in a murine asthma model (p < 0.05). we conclude that β-arrestin2 stimulated il-17 production  and expression of cd4+   t lymphocytes in a murine  asthma  model. the  effect  was partly mediated  by erk  1/2 activation. targeting β-arrestin2 biological activity could be a valid therapeutic approach for the treatment of allergic asthma.

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عنوان ژورنال:
iranian journal of allergy, asthma and immunology

جلد ۱۰، شماره ۳، صفحات ۱۷۱-۱۸۲

کلمات کلیدی
[ ' a s t h m a ' , ' β ' , ' a r r e s t i n 2 ' , ' c d 4 + t l y m p h o c y t e s ' , ' e x t r a c e l l u l a r s i g n a l ' , ' r e g u l a t e d k i n a s e 1 / 2 ' , ' i n t e r l e u k i n ' , 1 7 ]

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