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反式高尔基体网络(TGN)作为β1-肾上腺素能受体(β1AR)下调和再循环的调节节点。

Trans-Golgi Network (TGN) as a regulatory node for β1-adrenergic receptor (β1AR) down-modulation and recycling.

机构信息

Division of Hematology and Oncology, Rhode Island Hospital and Brown University, Providence, Rhode Island 02903, USA.

出版信息

J Biol Chem. 2012 Apr 20;287(17):14178-91. doi: 10.1074/jbc.M111.323782. Epub 2012 Feb 29.

Abstract

Receptor down-modulation is the key mechanism by which G protein-coupled receptors (GPCRs) prevent excessive receptor signaling in response to agonist stimulation. Recently, the trans-Golgi network (TGN) has been implicated as a key checkpoint for receptor endocytosis and degradation. Here, we investigated the involvement of the TGN in down-modulation of β1-adrenergic receptor in response to persistent isoprotenerol stimulation. Immunofluorescent staining showed that ~50% of endocytosed β1AR colocalized with TGN-46 at 5 h. Disruption of the TGN by brefeldin A (BFA) led to the robust accumulation of endocytosed β1AR in Rab11(+) recycling endosomes, inhibited β1AR entry into LAMP1(+) lysosomes, and as a result enhanced β1AR recycling to the plasma membrane. The lysosomotropic agent, chloroquine, arrested the majority of endocytosed β1AR in the TGN by 4 h. Immunoblot analysis showed that either disruption of the TGN or blockage of the lysosome prevented β1AR degradation. Co-expression of GFP-arrestin-3 in β1AR cells increased the endocytosis of β1AR and facilitated its entry to the TGN but inhibited recycling to the plasma membrane. Arrestin-3-induced inhibition of β1AR recycling was reversed by BFA treatment, whereas chloroquine induced the accumulation of arrestin-3 with β1AR in the TGN. These results demonstrate for the first time that the TGN acts as a checkpoint for both the recycling and down-regulation of β1AR and that arrestin-3 not only mediates β1AR endocytosis but also its recycling through the TGN.

摘要

受体内化和降解的调控枢纽。在此,我们研究了 TGN 在异丙肾上腺素持续刺激β1 肾上腺素能受体(β1AR)内化和降解中的作用。免疫荧光染色显示,在 5 小时时,约 50%的内化β1AR 与 TGN-46 共定位。布雷菲德菌素 A(BFA)破坏 TGN 导致内化的β1AR 大量积累在 Rab11(+)再循环内体中,抑制β1AR 进入 LAMP1(+)溶酶体,从而增强β1AR 向质膜的再循环。溶酶体趋向性药物氯喹在 4 小时内将大部分内化的β1AR 滞留在 TGN 中。免疫印迹分析表明,破坏 TGN 或阻断溶酶体均可阻止β1AR 降解。GFP-arrestin-3 在β1AR 细胞中的共表达增加了β1AR 的内化,并促进其进入 TGN,但抑制了向质膜的再循环。BFA 处理逆转了 arrestin-3 诱导的β1AR 再循环抑制,而氯喹诱导 arrestin-3 与β1AR 在 TGN 中的积累。这些结果首次证明 TGN 是β1AR 再循环和下调的调控枢纽,并且 arrestin-3 不仅介导β1AR 内化,还通过 TGN 介导其再循环。

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