Activation of TMEM16A by natural product canthaxanthin promotes gastrointestinal contraction

被引:12
|
作者
Ji, Qiushuang [1 ,2 ]
Shi, Sai [1 ,3 ]
Guo, Shuai [1 ,3 ]
Zhan, Yong [1 ,3 ]
Zhang, Hailin [4 ]
Chen, Yafei [1 ]
An, Hailong [1 ,3 ]
机构
[1] Hebei Univ Technol, Sch Sci, Inst Biophys, Key Lab Mol Biophys, Tianjin, Hebei, Peoples R China
[2] Tianjin Univ, Sch Pharmaceut Sci & Technol, Tianjin, Peoples R China
[3] Hebei Univ Technol, Sch Elect Engn, Tianjin, Peoples R China
[4] Hebei Med Univ, Dept Pharmacol, Key Lab Neural & Vasc Biol, Key Lab Pharmacol & Toxicol New Drug,Minist Educ, Shijiazhuang, Hebei, Peoples R China
来源
FASEB JOURNAL | 2020年 / 34卷 / 10期
基金
中国国家自然科学基金;
关键词
activator; binding site; canthaxanthin; ileal contraction; TMEM16A; CHLORIDE CHANNEL; INTERSTITIAL-CELLS; TRANSMEMBRANE PROTEIN; SWISS-MODEL; CL-CHANNEL; CAJAL; CONTRIBUTES; INHIBITION; EXPRESSION; CFTR;
D O I
10.1096/fj.202000443RR
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transmembrane 16A (TMEM16A), also known as anoctamin 1, is the molecular basis of the calcium-activated chloride channels. TMEM16A is present in interstitial cells of Cajal, which are the pacemaker cells that control smooth muscle contraction. TMEM16A is implicated in gastrointestinal disorders. Activation of TMEM16A is believed to promote the gastrointestinal muscle contraction. Here, we report a highly efficient, nontoxic, and selective activator of TMEM16A, canthaxanthin (CX). The study using molecular docking and site-directed mutation revealed that CX-specific binging site in TMEM16A is K769. CX was also found to promote the contraction of smooth muscle cells in gastrointestinal tract through activation of TMEM16A channels, which provides an excellent basis for development of CX as a chemical tool and potential therapeutic for gastrointestinal dysfunction.
引用
收藏
页码:13430 / 13444
页数:15
相关论文
共 50 条
  • [31] Ginsenoside Rb1, a novel activator of the TMEM16A chloride channel, augments the contraction of guinea pig ileum
    Guo, Shuai
    Chen, Yafei
    Pang, Chunli
    Wang, Xuzhao
    Qi, Jinlong
    Mo, Li
    Zhang, Hailin
    An, Hailong
    Zhan, Yong
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2017, 469 (5-6): : 681 - 692
  • [32] Expression of anoctamin 1/TMEM16A by interstitial cells of Cajal is fundamental for slow wave activity in gastrointestinal muscles
    Hwang, Sung Jin
    Blair, Peter J. A.
    Britton, Fiona C.
    O'Driscoll, Kate E.
    Hennig, Grant
    Bayguinov, Yulia R.
    Rock, Jason R.
    Harfe, Brian D.
    Sanders, Kenton M.
    Ward, Sean M.
    JOURNAL OF PHYSIOLOGY-LONDON, 2009, 587 (20): : 4887 - 4904
  • [33] Activation mechanism of the calcium-activated chloride channel TMEM16A revealed by cryo-EM
    Paulino, Cristina
    Kalienkova, Valeria
    Lam, Andy K. M.
    Neldner, Yvonne
    Dutzler, Raimund
    NATURE, 2017, 552 (7685) : 421 - +
  • [34] Activation mechanism of the calcium-activated chloride channel TMEM16A revealed by cryo-EM
    Cristina Paulino
    Valeria Kalienkova
    Andy K. M. Lam
    Yvonne Neldner
    Raimund Dutzler
    Nature, 2017, 552 : 421 - 425
  • [35] Mechanism of allosteric activation of TMEM16A/ANO1 channels by a commonly used chloride channel blocker
    Ta, Chau M.
    Adomaviciene, Aiste
    Rorsman, Nils J. G.
    Garnett, Hannah
    Tammaro, Paolo
    BRITISH JOURNAL OF PHARMACOLOGY, 2016, 173 (03) : 511 - 528
  • [36] Rotavirus toxin NSP4 induces diarrhea by activation of TMEM16A and inhibition of Na+ absorption
    Jiraporn Ousingsawat
    Myriam Mirza
    Yuemin Tian
    Eleni Roussa
    Rainer Schreiber
    David I. Cook
    Karl Kunzelmann
    Pflügers Archiv - European Journal of Physiology, 2011, 461 : 579 - 589
  • [37] Ca2+-activated Cl- channel TMEM16A inhibition by cholesterol promotes angiogenesis in endothelial cells
    Ma, Ke
    Liu, Sitong
    Liang, Hongyue
    Wang, Guan
    Wang, Tianyu
    Luo, Shuya
    Gao, Kuan
    Wang, Hui
    Liu, Mei
    Bai, Lichuan
    Xiao, Qinghuan
    JOURNAL OF ADVANCED RESEARCH, 2021, 29 : 23 - 32
  • [38] Rotavirus toxin NSP4 induces diarrhea by activation of TMEM16A and inhibition of Na+ absorption
    Ousingsawat, Jiraporn
    Mirza, Myriam
    Tian, Yuemin
    Roussa, Eleni
    Schreiber, Rainer
    Cook, David I.
    Kunzelmann, Karl
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2011, 461 (05): : 579 - 589
  • [39] A mutual activation loop between the Ca2+-activated chloride channel TMEM16A and EGFR/STAT3 signaling promotes breast cancer tumorigenesis
    Wang, Hui
    Yao, Fan
    Luo, Shuya
    Ma, Ke
    Liu, Mei
    Bai, Lichuan
    Chen, Si
    Song, Chang
    Wang, Tianyu
    Du, Qiang
    Wu, Huizhe
    Wei, Minjie
    Fang, Yue
    Xiao, Qinghuan
    CANCER LETTERS, 2019, 455 : 48 - 59
  • [40] Biochemical Inhibition of DOG1/TMEM16A Achieves Antitumoral Effects in Human Gastrointestinal Stromal Tumor Cells In Vitro
    Frobom, Robin
    Sellberg, Felix
    Xu, Cheng
    Zhao, Allan
    Larsson, Catharina
    Lui, Wenn-Onn
    Nilsson, Inga-Lena
    Berglund, Erik
    Branstrom, Robert
    ANTICANCER RESEARCH, 2019, 39 (07) : 3433 - 3442