Literature DB >> 22332421

[Mechanism of epithelial sodium channel (ENaC) regulation by cortactin: involvement of dynamin].

D V Ilatovskaia, T S Pavlov, Iu A Neguliaev, A V Starushchenko.   

Abstract

We have recently shown that epithelial sodium channels (ENaC) are regulated by the actin-binding protein cortactin via the Arp2/3 protein complex. However, it has been also demonstrated that GTPase, dynamin, which is known to regulate clathrin-mediated endocytosis, can as well initiate signaling cascades regulated by cortactin. This study was designed to investigate the involvement of dynamin into cortactin-mediated regulation of ENaC. Initially, a recently described inhibitor of dynamin, dynasore, was used. However, use of this inhibitor seemed to be inappropriate due to discovered side effects. F. i., treatment of mpkCCD(c14) cells monolayers with dynasore (in concentrations of 10 and 100 microM) resulted in a decrease in ENaC-mediated transepithelial currents. Besides, the same concentrations of dynasore caused reduced currents in CHO cells transfected with ENaC subunits. Therefore, the data demonstrated that dynasore down regulates both native and overexpressed channel's activity and is not suitable for studies of a role of dynamin in the clathrin-mediated endocytosis of ENaC. This effect is most likely caused either by dynasore's toxic effect upon the cells or by enhanced endocytosis of ENaC-activating proteins. In the following experiments designed to study the role of dynamin different plasmids encoding mutant forms of dynamin and cortactin were used. Dominant negative dynamin K44A transfected into CHO cells together with ENaC subunits significantly increased amiloride-sensitive current density compared to cells transfected with ENaC subunits only (control); additional transfection of cortactin in this system resulted in current density restitution back to the control level. Moreover, ENaC overexpression with the SH3 domain of cortactin, which is responsible for dynamin binding, caused a decrease if ENaC current. Thus, we have shown in this study that cortactin can mediate ENaC activity not only via the Arp2/3 complex, but apart from that dynamin and related processes also might be involved into ENaC regulation by cortactin.

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Year:  2011        PMID: 22332421

Source DB:  PubMed          Journal:  Tsitologiia        ISSN: 0041-3771


  4 in total

1.  Lipidomic and proteomic analysis of exosomes from mouse cortical collecting duct cells.

Authors:  Viet D Dang; Kishore Kumar Jella; Ragy R T Ragheb; Nancy D Denslow; Abdel A Alli
Journal:  FASEB J       Date:  2017-08-16       Impact factor: 5.191

Review 2.  Epithelial sodium channel (ENaC) family: Phylogeny, structure-function, tissue distribution, and associated inherited diseases.

Authors:  Israel Hanukoglu; Aaron Hanukoglu
Journal:  Gene       Date:  2016-01-07       Impact factor: 3.688

3.  Hepatitis B virus induces IL-23 production in antigen presenting cells and causes liver damage via the IL-23/IL-17 axis.

Authors:  Qinghong Wang; Jijun Zhou; Bei Zhang; Zhiqiang Tian; Jun Tang; Yanhua Zheng; Zemin Huang; Yi Tian; Zhengcai Jia; Yan Tang; Jennifer C van Velkinburgh; Qing Mao; Xiuwu Bian; Yifang Ping; Bing Ni; Yuzhang Wu
Journal:  PLoS Pathog       Date:  2013-06-27       Impact factor: 6.823

Review 4.  The Epithelial Sodium Channel and the Processes of Wound Healing.

Authors:  Silvia Chifflet; Julio A Hernandez
Journal:  Biomed Res Int       Date:  2016-07-14       Impact factor: 3.411

  4 in total

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