研究报告

钾离子通道蛋白Shaker对果蝇心脏衰老的保护作用

展开
  • 1. 南华大学衡阳医学院生物化学与分子生物学教研室,衡阳 421001
    2. 湖南师范大学心脏发育研究中心, 发育生物学与蛋白质组学教育部重点实验室,长沙 410081
刘学文,在读硕士研究生,专业方向:果蝇心衰的表观遗传调控。E-mail: 1547962520@qq.com

收稿日期: 2020-08-11

  修回日期: 2020-12-14

  网络出版日期: 2020-12-25

基金资助

国家自然科学基金项目编号(81500311,81711530050);湖南省科技厅课题资助编号(2015JC3080)

Potassium channel Shaker play a protective role against cardiac aging in Drosophila

Expand
  • 1. Department of Biochemistry and Molecular Biology, University of South China, Hengyang 421001, China
    2. Key Lab of MOE for Development Biology and Protein Chemistry, the Center for Heart Development, Hunan Normal University, Changsha 410081, China

Received date: 2020-08-11

  Revised date: 2020-12-14

  Online published: 2020-12-25

Supported by

Supported by the National Natural Science Foundation of China Nos(81500311,81711530050);Key Program of Hunan Provincial Department of Science and Technology No(2015JC3080)

摘要

钾离子通道在心肌细胞动作电位复极过程中起着重要作用。钾离子通道蛋白种类繁多,已知钾离子通道蛋白KCNQ和HERG/eag参与心脏动作电位的形成,调节心脏收缩节律。钾离子通道蛋白Shaker是果蝇(Drosophila)体内发现的第一个电压门控钾离子通道,维持神经元和肌肉细胞的电兴奋性,但是目前其在成人心脏功能中的作用仍不清楚。本研究以果蝇为模型,高频电刺激模拟心脏应激状态,观察钾离子通道蛋白shaker基因突变体的心衰发生率。同时,利用心脏特异性启动子hand4.2 Gal4特异性敲低钾离子通道蛋白Shaker的表达;果蝇成体心脏生理学功能分析系统分析了1、3、5周龄特异性敲低钾离子通道蛋白Shaker的心脏表型。结果表明,shaker基因突变将严重影响果蝇心脏抗应激能力,表现在高频电刺激后的心力衰竭发生率显著性升高;心脏特异性敲低shaker基因导致5周龄果蝇心律失常发生率显著性增加;心脏特异性敲低HDAC3将显著降低果蝇寿命。综上所述,本研究推测钾离子通道蛋白Shaker在衰老过程中维护果蝇正常的心脏功能。

本文引用格式

刘学文, 吴红梅, 白瑛, 曾群, 曹泽民, 吴秀山, 唐旻 . 钾离子通道蛋白Shaker对果蝇心脏衰老的保护作用[J]. 遗传, 2021 , 43(1) : 94 -99 . DOI: 10.16288/j.yczz.20-253

Abstract

Potassium channels, which are the most diverse group of the ion channel family, play an important role in the repolarization of cardiomyocytes. Recent studies showed that potassium channels, such as KCNQ and HERG/eag, play an important role in regulating adult heart function through shaping the action potential and maintaining the rhythm of cardiac contraction. The potassium channel protein Shaker is the first voltage-gated potassium channel found in Drosophila to maintain the electrical excitability of neurons and muscle cells, but its role in adult cardiac function is still unclear. In this study, Drosophila was used as a model to study the role of Shaker channel in the maintenance of cardiac function under stress and aging. The incidence of heart failure was observed in shaker mutant after external electrical pacing, which simulates cardiac stress. Additionally, The cardiac-specific driver hand4.2 Gal4 was used to specifically knock down the expression of the potassium channel shaker in Drosophila. The cardiac parameter was analyzed at 1, 3, 5 weeks of age on cardiac specific knockdown of shaker using Drosophila adult cardiac physiological assay. The results showed that the mutation of shaker gene seriously affect the cardiac function under stress, demonstrated by significant increase in heart failure rate under electrical stimulation. In addition, cardiac specific knockdown of shaker increased the incidence of arrhythmias in Drosophila at the age of 5 weeks. Cardiac-specific knockdown of shaker reduces life span. Therefore, the results of this study suggest a vital role of the potassium channel shaker in maintaining normal cardiac function during aging.

参考文献

[1] Curtis AB, Karki R, Hattoum A, Sharma UC . Arrhythmias in patients ≥80 years of age: pathophysiology, management, and outcomes. J Am Coll Cardiol, 2018,71(18):2041-2057.
[2] Jeevaratnam K, Chadda KR, Huang CLH, Camm AJ . Cardiac potassium channels: physiological insights for targeted therapy. J Cardiovasc Pharmacol Ther, 2018,23(2):119-129.
[3] Schmitt N, Grunnet M, Olesen SP . Cardiac potassium channel subtypes: new roles in repolarization and arrhythmia. Physiol Rev, 2014,94(2):609-653.
[4] Giudicessi JR, Ackerman MJ . Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy. Nat Rev Cardiol, 2012,9(6):319-332.
[5] Tomson TT, Arora R . Modulation of cardiac potassium current by neural tone and ischemia. Card Electrophysiol Clin, 2016,8(2):349-360.
[6] Grunnet M, Behr ER, Calloe K, Hofman-Bang J, Till J, Christiansen M, McKenna WJ, Olesen SP, Schmitt N. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome. Heart Rhythm, 2005,2(11):1238-1249.
[7] Ocorr K, Reeves NL, Wessells RJ, Fink M, Chen HSV, Akasaka T, Yasuda S, Metzger JM, Giles W, Posakony JW, Bodmer R . KCNQ potassium channel mutations cause cardiac arrhythmias in Drosophila that mimic the effects of aging. Proc Natl Acad Sci USA, 2007,104(10):3943-3948.
[8] Sanguinetti MC , Tristani-Firouzi M. hERG potassium channels and cardiac arrhythmia. Nature, 2006,440(7083):463-469.
[9] Ocorr K, Zambon A, Nudell Y, Pineda S, Diop S, Tang M, Akasaka T, Taylor E . Age-dependent electrical and morphological remodeling of the Drosophila heart caused by hERG/seizure mutations. PLoS Genet, 2017,13(5):e1006786.
[10] Rivlin PK, St Clair RM, Vilinsky I, Deitcher DL . Morphology and molecular organization of the adult neuromuscular junction of Drosophila. J Comp Neurol, 2004,468(4):596-613.
[11] Ruiz-Ca?ada C, Koh YH, Budnik V, Tejedor FJ . DLG differentially localizes Shaker K+-channels in the central nervous system and retina of Drosophila. J Neurochem, 2002,82(6):1490-1501.
[12] Wessells RJ, Bodmer R . Screening assays for heart function mutants in Drosophila. Biotechniques, 2004,37(1):58-60.
[13] Zhang YY, Tang M, Xia Q, Li RL, Deng ZW, Peng XW, Yuan WZ, Wu XS . The Drosophila pacing model for screening the 2nd chromsome deficiency lines related to heart failure. Life Science Research, 2010,14(3):4.
[13] 张艳阳, 唐旻, 夏琼, 李冉林, 邓志伟, 彭向文, 袁婺洲, 吴秀山 . 利用果蝇心力衰竭模型筛选果蝇第2号染色体缺失系. 生命科学研究, 2010,14(3):4.
[14] Fink M, Callol-Massot C, Chu A, Ruiz-Lozano P, Izpisua Belmonte JC, Giles W, Bodmer R, Ocorr K . A new method for detection and quantification of heartbeat parameters in Drosophila, zebrafish, and embryonic mouse hearts. Biotechniques, 2009,46(2):101-113.
[15] Wessells RJ, Fitzgerald E, Cypser JR, Tatar M, Bodmer R . Insulin regulation of heart function in aging fruit flies. Nat Genet, 2004,36(12):1275-1281.
[16] Ocorr K, Fink M, Cammarato A, Bernstein S, Bodmer R . Semi-automated optical heartbeat analysis of small hearts. J Vis Exp, 2009,31(31):e1435.
[17] Lichtinghagen R, Stocker M, Wittka R, Boheim G, Stühmer W, Ferrus A, Pongs O . Molecular basis of altered excitability in Shaker mutants of Drosophila melanogaster. EMBO J, 1990,9(13):4399-4407.
[18] Nishimura M, Ocorr K, Bodmer R, Cartry J . Drosophila as a model to study cardiac aging. Exp Gerontol, 2011,46(5):326-330.
[19] Horn MA . Cardiac physiology of aging: extracellular considerations. Compr Physiol, 2015,5(3):1069-1121.
[20] Hughes CJR, Jacobs JR . Dissecting the role of the extracellular matrix in heart disease: lessons from the Drosophila genetic model. Vet Sci, 2017,4(2):24.
文章导航

/