Constitutive activity of NADPH oxidase 1 (Nox1) that promotes its own activity suppresses the colon epithelial cell migration

被引:8
作者
Miyano, Kei [1 ]
Okamoto, Shuichiro [1 ]
Yamauchi, Akira [1 ]
Kajikawa, Mizuho [2 ]
Kiyohara, Takuya [3 ]
Taura, Masahiko [4 ]
Kawai, Chikage [1 ]
Kuribayashi, Futoshi [1 ]
机构
[1] Kawasaki Med Sch, Dept Biochem, 577 Matsushima, Kurashiki, Okayama 7010192, Japan
[2] Showa Pharmaceut Univ, Lab Microbiol, Machida, Tokyo, Japan
[3] Hakujyuji Hosp, Dept Cerebrovasc Dis & Neurol, Fukuoka, Japan
[4] Fukuoka Univ, Fac Med, Dept Otorhinolaryngol, Fukuoka, Japan
关键词
NOX1; NADPH oxidase; ROS; epithelial cells; cell migration; edaravone; FORMYL PEPTIDE RECEPTOR; SUPEROXIDE-PRODUCTION; ACTIVATION; GLYCOSYLATION; INVOLVEMENT; GENERATION; PROTEINS; SRC;
D O I
10.1080/10715762.2020.1823383
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
Superoxide producing NADPH oxidase 1 (Nox1), abundantly expressed in the colon epithelium, plays a crucial role in mucosal host defenses. In this study, we found that pre-treatment of cells with edaravone, a free radical scavenger, inhibited Nox1 constitutive activity even after washout without affecting Nox1 trafficking to the plasma membrane and membrane recruitment of the cytosolic regulators Noxo1 and Noxa1. These results suggest that a Nox1-derived product is involved in the step that initiates the electron transfer reaction after the formation of the Nox1-Noxo1-Noxa1 complex. Furthermore, we show that the mean migration directionality and velocity of epithelial cells were significantly enhanced by the inhibition of constitutive Nox1 activity. Thus, the constitutive Nox1 activity limits undesired cell migration in resting cells while participating in a positive feedback loop toward its own oxidase activity.
引用
收藏
页码:640 / 648
页数:9
相关论文
共 37 条
[1]   The reaction rate of edaravone (3-methyl-1-phenyl-2-pyrazolin-5-one (MCI-186)) with hydroxyl radical [J].
Abe, S ;
Kirima, K ;
Tsuchiya, K ;
Okamoto, M ;
Hasegawa, T ;
Houchi, H ;
Yoshizumi, M ;
Tamaki, T .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2004, 52 (02) :186-191
[2]   Redox signaling regulates commensal-mediated mucosal homeostasis and restitution and requires formyl peptide receptor 1 [J].
Alam, A. ;
Leoni, G. ;
Wentworth, C. C. ;
Kwal, J. M. ;
Wu, H. ;
Ardita, C. S. ;
Swanson, P. A. ;
Lambeth, J. D. ;
Jones, R. M. ;
Nusrat, A. ;
Neish, A. S. .
MUCOSAL IMMUNOLOGY, 2014, 7 (03) :645-655
[3]   Two novel proteins activate superoxide generation by the NADPH oxidase NOX1 [J].
Bánfi, B ;
Clark, RA ;
Steger, K ;
Krause, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :3510-3513
[4]   Nox family NADPH oxidases: Molecular mechanisms of activation [J].
Brandes, Ralf P. ;
Weissmann, Norbert ;
Schroeder, Katrin .
FREE RADICAL BIOLOGY AND MEDICINE, 2014, 76 :208-226
[5]   NOXO1, regulation of lipid binding, localization, and activation of Nox1 by the phox homology (PX) domain [J].
Cheng, GJ ;
Lambeth, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (06) :4737-4742
[6]   Nox1-dependent reactive oxygen generation is regulated by Rac1 [J].
Cheng, Guangjie ;
Diebold, Becky A. ;
Hughes, Yasmin ;
Lambeth, J. David .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (26) :17718-17726
[7]   Modulation of epithelial cell adhesion in gastrointestinal homeostasis [J].
Efstathiou, JA ;
Pignatelli, M .
AMERICAN JOURNAL OF PATHOLOGY, 1998, 153 (02) :341-347
[8]  
Fisher AB, 2009, ANTIOXID REDOX SIGN, V11, P1349, DOI [10.1089/ars.2008.2378, 10.1089/ARS.2008.2378]
[9]   Proteins homologous to p47phox and p67phox support superoxide production by NAD(P)H oxidase 1 in colon epithelial cells [J].
Geiszt, M ;
Lekstrom, K ;
Witta, J ;
Leto, TL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (22) :20006-20012
[10]   The involvement of the tyrosine kinase c-Src in the regulation of reactive oxygen species generation mediated by NADPH oxidase-1 [J].
Gianni, Davide ;
Bohl, Ben ;
Courtneidge, Sara A. ;
Bokoch, Gary M. .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (07) :2984-2994