Hunyady Laszlo, Baukal Albert J, Gaborik Zsuzsanna, Olivares-Reyes Jesus A, Bor Marta, Szaszak Marta, Lodge Robert, Catt Kevin J, Balla Tamas
Endocrinology and Reproduction Research Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
J Cell Biol. 2002 Jun 24;157(7):1211-22. doi: 10.1083/jcb.200111013. Epub 2002 Jun 17.
Agonist-induced endocytosis and processing of the G protein-coupled AT1 angiotensin II (Ang II) receptor (AT1R) was studied in HEK 293 cells expressing green fluorescent protein (GFP)- or hemagglutinin epitope-tagged forms of the receptor. After stimulation with Ang II, the receptor and its ligand colocalized with Rab5-GFP and Rab4-GFP in early endosomes, and subsequently with Rab11-GFP in pericentriolar recycling endosomes. Inhibition of phosphatidylinositol (PI) 3-kinase by wortmannin (WT) or LY294002 caused the formation of large endosomal vesicles of heterogeneous Rab composition, containing the ligand-receptor complex in their limiting membranes and in small associated vesicular structures. In contrast to Alexa(R)-transferrin, which was mainly found in small vesicles associated with the outside of large vesicles in WT-treated cells, rhodamine-Ang II was also segregated into small internal vesicles. In cells labeled with 125I-Ang II, WT treatment did not impair the rate of receptor endocytosis, but significantly reduced the initial phase of receptor recycling without affecting its slow component. Similarly, WT inhibited the early, but not the slow, component of the recovery of AT1R at the cell surface after termination of Ang II stimulation. These data indicate that internalized AT1 receptors are processed via vesicles that resemble multivesicular bodies, and recycle to the cell surface by a rapid PI 3-kinase-dependent recycling route, as well as by a slower pathway that is less sensitive to PI 3-kinase inhibitors.
在表达绿色荧光蛋白(GFP)或血凝素表位标记形式受体的人胚肾293(HEK 293)细胞中,研究了激动剂诱导的G蛋白偶联的1型血管紧张素II(Ang II)受体(AT1R)的内吞作用和加工过程。用Ang II刺激后,受体及其配体在早期内体中与Rab5-GFP和Rab4-GFP共定位,随后在中心粒周围回收内体中与Rab11-GFP共定位。渥曼青霉素(WT)或LY294002对磷脂酰肌醇(PI)3激酶的抑制导致形成具有异质Rab组成的大内体囊泡,其限制膜和小的相关囊泡结构中含有配体-受体复合物。与主要存在于WT处理细胞中大囊泡外部相关小囊泡中的Alexa(R)-转铁蛋白不同,罗丹明-Ang II也被分隔到小的内部囊泡中。在用125I-Ang II标记的细胞中,WT处理不损害受体内吞作用的速率,但显著降低受体回收的初始阶段,而不影响其缓慢成分。同样,WT抑制Ang II刺激终止后细胞表面AT1R恢复的早期成分,但不抑制缓慢成分。这些数据表明,内化的AT1受体通过类似于多囊泡体的囊泡进行加工,并通过快速的PI 3激酶依赖性回收途径以及对PI 3激酶抑制剂不太敏感的较慢途径再循环到细胞表面。