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Action of Protein Tyrosine Kinase Inhibitors on the Hypotonicity-Stimulated Trafficking Kinetics of Epithelial Na+ Channels (ENaC) in Renal Epithelial Cells: Analysis Using a Mathematical Model
Author(s) -
Rie Marunaka,
Akiyuki Taruno,
Toshiro Yamamoto,
Narisato Kanamura,
Yoshinori Marunaka
Publication year - 2018
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000494012
Subject(s) - epithelial sodium channel , tyrosine kinase , kinetics , chemistry , microbiology and biotechnology , tyrosine kinase inhibitor , protein kinase a , endocrinology , medicine , pharmacology , biophysics , phosphorylation , biology , signal transduction , biochemistry , sodium , physics , quantum mechanics , cancer , organic chemistry
Epithelial Na+ channels (ENaCs) play crucial roles in control of blood pressure by determining the total amount of renal Na+ reabsorption, which is regulated by various factors such as aldosterone, vasopressin, insulin and osmolality. The intracellular trafficking process of ENaCs regulates the amount of the ENaC-mediated Na+ reabsorption in the collecting duct of the kidney mainly by determining the number of ENaC expressed at the apical membrane of epithelial cells. Although we previously reported protein tyrosine kinases (PTKs) contributed to the ENaC-mediated epithelial Na+ reabsorption, we have no information on the role of PTKs in the intracellular ENaC trafficking.

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