Suppr超能文献

血管紧张素转换酶2胞质尾内钙调蛋白结合结构域的鉴定。

The identification of a calmodulin-binding domain within the cytoplasmic tail of angiotensin-converting enzyme-2.

作者信息

Lai Zon W, Lew Rebecca A, Yarski Michael A, Mu Fi-Tjen, Andrews Robert K, Smith A Ian

机构信息

Department of Biochemistry and Molecular Biology, Monash University, Wellington Road, Clayton, Victoria 3800, Australia.

出版信息

Endocrinology. 2009 May;150(5):2376-81. doi: 10.1210/en.2008-1274. Epub 2009 Jan 22.

Abstract

Angiotensin-converting enzyme (ACE)-2 is a homolog of the well-characterized plasma membrane-bound angiotensin-converting enzyme. ACE2 is thought to play a critical role in regulating heart function, and in 2003, ACE2 was identified as a functional receptor for severe acute respiratory syndrome coronavirus. We have recently shown that like ACE, ACE2 undergoes ectodomain shedding and that this shedding event is up-regulated by phorbol esters. In the present study, we used gel shift assays to demonstrate that calmodulin, an intracellular calcium-binding protein implicated in the regulation of other ectodomain shedding events, binds a 16-amino acid synthetic peptide corresponding to residues 762-777 within the cytoplasmic domain of human ACE2, forming a calcium-dependent calmodulin-peptide complex. Furthermore, we have demonstrated that ACE2 expressed in Chinese hamster ovary cells specifically binds to glutathione-S-transferase-calmodulin, but not glutathione-S-transferase alone, in pull-down assays using cell lysates. Finally, to investigate whether calmodulin has any effect on ACE2 ectodomain shedding in cells that endogenously express the enzyme, cells from a human liver cell line (Huh-7) expressing ACE2 were incubated with calmodulin-specific inhibitors, trifluoperazine and calmidazolium. Both trifluoperazine (25 micromol/liter) and calmidazolium, (25 micromol/liter) significantly increased the release of ACE2 into the medium (44.1 +/- 10.8%, P < 0.05, Student's t test; unpaired, two-tailed, and 51.1 +/- 7.4% P < 0.05, one-way ANOVA, respectively;), as analyzed by an ACE2-specific quenched fluorescence substrate assay. We also show that the calmodulin-specific inhibitor-stimulated shedding of ACE2 is independent from phorbol ester-induced shedding. In summary, we have demonstrated that calmodulin is able to bind ACE2 and suggest that the ACE2 ectodomain shedding and/or sheddase(s) activation regulated by calmodulin is independent from the phorbol ester-induced shedding.

摘要

血管紧张素转换酶2(ACE)-2是一种已被充分表征的质膜结合型血管紧张素转换酶的同源物。ACE2被认为在调节心脏功能中起关键作用,并且在2003年,ACE2被鉴定为严重急性呼吸综合征冠状病毒的功能性受体。我们最近发现,与ACE一样,ACE2也会发生胞外域脱落,并且这种脱落事件会被佛波酯上调。在本研究中,我们使用凝胶迁移试验证明钙调蛋白(一种参与调节其他胞外域脱落事件的细胞内钙结合蛋白)与人ACE2胞质域内762 - 777位残基对应的16个氨基酸合成肽结合,形成钙依赖性钙调蛋白 - 肽复合物。此外,在使用细胞裂解物的下拉试验中,我们证明了在中国仓鼠卵巢细胞中表达的ACE2特异性结合谷胱甘肽 - S - 转移酶 - 钙调蛋白,而不单独结合谷胱甘肽 - S - 转移酶。最后,为了研究钙调蛋白对内源表达该酶的细胞中ACE2胞外域脱落是否有任何影响,将来自表达ACE2的人肝癌细胞系(Huh - 7)的细胞与钙调蛋白特异性抑制剂三氟拉嗪和氯米帕明一起孵育。通过ACE2特异性淬灭荧光底物测定分析,三氟拉嗪(25微摩尔/升)和氯米帕明(25微摩尔/升)均显著增加了ACE2释放到培养基中的量(分别为44.1±10.8%,P < 0.05,Student t检验;不成对,双侧;以及51.1±7.4%,P < 0.05,单因素方差分析)。我们还表明,钙调蛋白特异性抑制剂刺激的ACE2脱落与佛波酯诱导的脱落无关。总之,我们证明了钙调蛋白能够结合ACE2,并表明由钙调蛋白调节的ACE2胞外域脱落和/或裂解酶激活与佛波酯诱导的脱落无关。

相似文献

8
Ectodomain shedding of angiotensin converting enzyme 2 in human airway epithelia.人呼吸道上皮细胞中血管紧张素转换酶2的胞外域脱落
Am J Physiol Lung Cell Mol Physiol. 2009 Jul;297(1):L84-96. doi: 10.1152/ajplung.00071.2009. Epub 2009 May 1.

引用本文的文献

3
Circulating angiotensin converting enzyme 2 and COVID-19.循环血管紧张素转换酶2与新型冠状病毒肺炎
World J Clin Cases. 2022 Dec 6;10(34):12470-12483. doi: 10.12998/wjcc.v10.i34.12470.
6
ACE2 Shedding and the Role in COVID-19.ACE2 脱落及其在 COVID-19 中的作用。
Front Cell Infect Microbiol. 2022 Jan 14;11:789180. doi: 10.3389/fcimb.2021.789180. eCollection 2021.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验