Che Pulin, Chen Yunjia, Lu Roujian, Peng Ning, Gannon Mary, Wyss J Michael, Jiao Kai, Wang Qin
Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, 1918 University Boulevard, Birmingham, AL 35294, United States of America.
the National Institute for Viral Disease Control and Prevention, China CDC, Beijing, China.
PLoS One. 2015 Aug 5;10(8):e0135030. doi: 10.1371/journal.pone.0135030. eCollection 2015.
The α2 adrenergic receptor (AR) subtypes are important for blood pressure control. When activated, the α2A subtype elicits a hypotensive response whereas the α2B subtype mediates a hypertensive effect that counteracts the hypotensive response by the α2A subtype. We have previously shown that spinophilin attenuates the α2AAR-dependent hypotensive response; in spinophilin null mice, this response is highly potentiated. In this study, we demonstrate that spinophilin impedes arrestin-dependent phosphorylation and desensitization of the α2BAR subtype by competing against arrestin binding to this receptor subtype. The Del301-303 α2BAR, a human variation that shows impaired phosphorylation and desensitization and is linked to hypertension in certain populations, exhibits preferential interaction with spinophilin over arrestin. Furthermore, Del301-303 α2BAR-induced ERK signaling is quickly desensitized in cells without spinophilin expression, showing a profile similar to that induced by the wild type receptor in these cells. Together, these data suggest a critical role of spinophilin in sustaining α2BAR signaling. Consistent with this notion, our in vivo study reveals that the α2BAR-elicited hypertensive response is diminished in spinophilin deficient mice. In arrestin 3 deficient mice, where the receptor has a stronger binding to spinophilin, the same hypertensive response is enhanced. These data suggest that interaction with spinophilin is indispensable for the α2BAR to elicit the hypertensive response. This is opposite of the negative role of spinophilin in regulating α2AAR-mediated hypotensive response, suggesting that spinophilin regulation of these closely related receptor subtypes can result in distinct functional outcomes in vivo. Thus, spinophilin may represent a useful therapeutic target for treatment of hypertension.
α2肾上腺素能受体(AR)亚型对血压控制至关重要。激活后,α2A亚型会引发降压反应,而α2B亚型介导升压作用,抵消α2A亚型的降压反应。我们之前已经表明,亲嗜素会减弱α2AAR依赖性降压反应;在亲嗜素基因敲除小鼠中,这种反应会被高度增强。在本研究中,我们证明亲嗜素通过与抑制蛋白竞争结合该受体亚型,阻碍了α2BAR亚型的抑制蛋白依赖性磷酸化和脱敏。Del301 - 303 α2BAR是一种人类变体,表现出磷酸化和脱敏受损,在某些人群中与高血压有关,它与亲嗜素的相互作用比与抑制蛋白的相互作用更优先。此外,在没有亲嗜素表达的细胞中,Del301 - 303 α2BAR诱导的ERK信号传导会迅速脱敏,显示出与野生型受体在这些细胞中诱导的情况相似的特征。总之,这些数据表明亲嗜素在维持α2BAR信号传导中起关键作用。与此观点一致,我们的体内研究表明,在亲嗜素缺陷小鼠中,α2BAR引发的升压反应减弱。在抑制蛋白3缺陷小鼠中,受体与亲嗜素的结合更强,相同的升压反应增强。这些数据表明,与亲嗜素的相互作用对于α2BAR引发升压反应是必不可少的。这与亲嗜素在调节α2AAR介导的降压反应中的负作用相反,表明亲嗜素对这些密切相关的受体亚型的调节在体内可导致不同的功能结果。因此,亲嗜素可能是治疗高血压的一个有用的治疗靶点。