| Home  | About ScienceAsia  | Publication charge  | Advertise with us  | Subscription for printed version  | Contact us  
Editorial Board
Journal Policy
Instructions for Authors
Online submission
Author Login
Reviewer Login
Volume 50 Number 2
Volume 50 Number 1
Volume 49 Number 6
Volume 49 Number 5
Volume 49S Number 1
Volume 49 Number 4
Earlier issues Botak Empire
Maxwin Botak Empire
Botak Empire Scatter
Daftar Botak Empire
Botak Empire Rekomendasi
Botak Empire Menang
Botak Empire Akun Pro
Scatter Botak Empire
Botak Empire Deposit Receh
Empire88 Slot 4D
Botak Empire Alternatif
Volume  Number 

previous article next article

Research articles

ScienceAsia (): 332-339 |doi: 10.2306/scienceasia1513-1874...332

Nongenomic effect of aldosterone on angiotensin II type 1 receptor dimerization in human renal proximal tubular cells: Implications for endoplasmic reticulum stress

Kittisak Sinphitukkula,g, Krissanapong Manothamb, Somchai Eiam-Ongc, Masaomi Nangakud, Reiko Inagie, Somchit Eiam-Ongf,*

ABSTRACT:     In vitro studies have showed that aldosterone increases oxidative stress molecules through a nongenomic effect. Oxidative stress induces angiotensin II type 1 receptor (AT1R) dimerization and endoplasmic reticulum (ER) stress, leading to renal tubular damage. However, the nongenomic effect of aldosterone on AT1R dimerization and ER stress in renal cells has not been determined. Here, we examined the nongenomic action of aldosterone in renal proximal tubular epithelial cells (PTECs) to better understand the underlying mechanisms. HK-2 cells, human renal PTECs, were exposed to vehicle or aldosterone for 30 min. In two additional groups, the cells were pretreated with eplerenone, a mineralocorticoid receptor (MR) blocker or apocynin, an NADPH oxidase inhibitor, for 30 min before aldosterone incubation. Protein abundances of dimeric/monomeric forms of AT1R, p47phox (a cytosolic part of NADPH oxidase), and activating transcription factor 4 (ATF4), a transcription factor responsive to ER stress, were determined by Western blotting. Aldosterone nongenomically increased plasma membrane protein expression of AT1R dimeric forms in a time- and dose-dependent manners. The levels of the cytosolic p47phox protein declined while the membranous protein level was enhanced following aldosterone treatment. The aldosterone induced alteration in these two proteins was abolished by pretreatment with eplerenone or apocynin. In addition, aldosterone (100 nM) induced nuclear ATF4 protein accumulation in a time-dependent fashion, which was blocked by apocynin and partially attenuated by eplerenone. Aldosterone nongenomically increased AT1R dimerization and nuclear ATF4 protein accumulation dependent on MR and NADPH oxidase activation. Hence aldosterone could induce AT1R dimerization and activate the endoplasmic reticulum stress response.

Download PDF

60 Downloads 2007 Views

a Graduate Division, Faculty of Medicine, Chulalongkorn University, Bangkok 10330 Thailand
b Renal Unit, Department of Medicine, Lerdsin General Hospital, Bangkok 10330 Thailand
c Department of Medicine (Division of Nephrology), Faculty of Medicine, Chulalongkorn University, Bangkok 10330 Thailand
d Division of Nephrology and Endocrinology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655 Japan
e Division of Chronic Kidney Disease Pathophysiology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655 Japan
f Department of Physiology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330 Thailand
g Faculty of Medicine, Siam University, Bangkok 10160 Thailand

* Corresponding author, E-mail:

Received 6 Jan 2018, Accepted 17 Sep 2018