Department of Pharmacology, Faculty of Medicine, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan.
J Membr Biol. 2013 Jul;246(7):571-9. doi: 10.1007/s00232-013-9571-6. Epub 2013 Jun 19.
In cardiomyocytes, β1-adrenergic receptor (β1-AR) plays an important role in regulating cardiac functions. Upon continuous ligand stimulation, β1-AR is internalized and mostly recycled back to the plasma membrane (PM). The recycling endosome (RE) is one of the membranous organelles involved in the protein recycling pathway. To determine whether RE is involved in the internalization of β1-AR upon ligand stimulation, we evaluated the localization of β1-AR after stimulation with a β-agonist, isoproterenol (Iso), in β1-AR-transfected COS-1 cells. After 30 min of Iso treatment and cell surface labeling with the appropriate antibodies, β1-AR was internalized from PM and translocated into the perinuclear region, the same location as the transferrin receptor, an RE marker. We then evaluated whether sorting nexin 27 (SNX27) participated in the β1-AR recycling pathway. When β1-AR and SNX27 were coexpressed, β1-AR coimmunoprecipitated with SNX27. In addition, shRNA-mediated silencing of SNX27 compromised β1-AR recycling and enhanced its delivery into lysosome. Overall, β1-AR on PM was internalized into RE upon Iso stimulation and recycled by RE through binding with SNX27 in COS-1 cells.
在心肌细胞中,β1-肾上腺素能受体(β1-AR)在调节心脏功能方面起着重要作用。在持续的配体刺激下,β1-AR 被内化并大部分回收回到质膜(PM)。再循环内体(RE)是参与蛋白质再循环途径的膜细胞器之一。为了确定 RE 是否参与配体刺激下的β1-AR 内化,我们在转染了β1-AR 的 COS-1 细胞中评估了β-激动剂异丙肾上腺素(Iso)刺激后β1-AR 的定位。用适当的抗体进行细胞表面标记后,经过 30 分钟的 Iso 处理,β1-AR 从 PM 内化并转移到核周区域,与转铁蛋白受体(RE 标志物)的位置相同。然后,我们评估了分选连接蛋白 27(SNX27)是否参与了β1-AR 再循环途径。当β1-AR 和 SNX27 共表达时,β1-AR 与 SNX27 共免疫沉淀。此外,shRNA 介导的 SNX27 沉默削弱了β1-AR 的再循环,并增强了其向溶酶体的输送。总之,在 COS-1 细胞中,PM 上的β1-AR 在 Iso 刺激下被内化到 RE 中,并通过与 SNX27 结合由 RE 回收。