Publication: Oxidative stress increases angiotensin receptor type i responsiveness by increasing receptor degree of aggregation using image correlation spectroscopy
Issued Date
2011-10-01
Resource Type
ISSN
18792642
00052736
00052736
Other identifier(s)
2-s2.0-79961121915
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Biochimica et Biophysica Acta - Biomembranes. Vol.1808, No.10 (2011), 2496-2500
Suggested Citation
Titiwat Sungkaworn, Yongwimon Lenbury, Varanuj Chatsudthipong Oxidative stress increases angiotensin receptor type i responsiveness by increasing receptor degree of aggregation using image correlation spectroscopy. Biochimica et Biophysica Acta - Biomembranes. Vol.1808, No.10 (2011), 2496-2500. doi:10.1016/j.bbamem.2011.07.007 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/11455
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Oxidative stress increases angiotensin receptor type i responsiveness by increasing receptor degree of aggregation using image correlation spectroscopy
Other Contributor(s)
Abstract
Oxidative stress and hyper-functioning of angiotensin II receptor type I (AT 1 R) are commonly observed in hypertensive patients but the relationship between oxidative stress and AT 1 R function is still unclear. We investigated the effects of H 2 O 2 treatment on AT 1 R-mediated intracellular calcium [Ca 2+ ] i signaling and its cell surface distribution pattern in HEK cells stably expressing EGFP-tagged rat AT 1 R using image correlation spectroscopy (ICS). Following H 2 O 2 treatment (50-800 μM), [Ca 2+ ] i was significantly increased upon angiotensin II stimulation. Similarly ICS revealed a significant increase in degree of AT 1 R aggregation in H 2 O 2 treated group during Ang II activation but no difference in cluster density compared with untreated control cells or those with N-acetyl cysteine pretreatment. Thus, oxidative stress-induced AT 1 R hyper-responsiveness can be attributed by an increase in cell surface receptor aggregation state, possibly stemming in part from oxidant-related increase receptor-receptor interactions. © 2011 Elsevier B.V. All rights reserved.