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胰高血糖素样肽-1受体的同源脱敏和内化速率。

Rate of Homologous Desensitization and Internalization of the GLP-1 Receptor.

作者信息

Shaaban Ghina, Oriowo Mabayoje, Al-Sabah Suleiman

机构信息

Department of Pharmacology & Toxicology, Faculty of Medicine, Kuwait University, PO Box 24923, 13110 Safat, Kuwait.

出版信息

Molecules. 2016 Dec 26;22(1):22. doi: 10.3390/molecules22010022.

Abstract

The glucagon-like peptide-1 receptor (GLP-1R) is an important target in the treatment of type 2 diabetes mellitus. The aim of this study was to compare the rate of agonist stimulated desensitization and internalization of GLP-1R. To this end, an N-terminally myc-tagged GLP-1R was stably expressed in HEK-293 cells. Homologous desensitization was assessed by measuring the cAMP response to agonist stimulation following pre-incubation with agonist for up to 120 min. Receptor internalization was monitored using an indirect ELISA-based method and confocal microscopy. Pre-incubation with GLP-1 resulted in a time-dependent loss of response to a second stimulation. Washing cells following pre-incubation failed to bring cAMP levels back to basal. Taking this into account, two desensitization rates were calculated: "apparent" (t = 19.27 min) and "net" (t = 2.99 min). Incubation of cells with GLP-1 also resulted in a time-dependent loss of receptor cell surface expression (t = 2.05 min). Rapid agonist-stimulated internalization of GLP-1R was confirmed using confocal microscopy. Stimulation of GLP-1R with GLP-1 results in rapid desensitization and internalization of the receptor. Interestingly, the rate of "net" desensitization closely matches the rate of internalization. Our results suggest that agonist-bound GLP-1R continues to generate cAMP after it has been internalized.

摘要

胰高血糖素样肽-1受体(GLP-1R)是2型糖尿病治疗中的一个重要靶点。本研究的目的是比较激动剂刺激下GLP-1R脱敏和内化的速率。为此,在HEK-293细胞中稳定表达了N端带有myc标签的GLP-1R。通过在长达120分钟的时间内用激动剂预孵育后测量对激动剂刺激的cAMP反应来评估同源脱敏。使用基于间接ELISA的方法和共聚焦显微镜监测受体内化。用GLP-1预孵育导致对第二次刺激的反应随时间丧失。预孵育后洗涤细胞未能使cAMP水平恢复到基础水平。考虑到这一点,计算了两种脱敏速率:“表观”(t = 19.27分钟)和“净”(t = 2.99分钟)。用GLP-1孵育细胞也导致受体细胞表面表达随时间丧失(t = 2.05分钟)。使用共聚焦显微镜证实了GLP-1R激动剂刺激后的快速内化。用GLP-1刺激GLP-1R会导致受体快速脱敏和内化。有趣的是,“净”脱敏速率与内化速率密切匹配。我们的结果表明,与激动剂结合的GLP-1R内化后仍继续产生cAMP。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa98/6155907/c0c09a8725a0/molecules-22-00022-g001.jpg

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