Molecular mechanisms of the antagonistic action between AT(1) and AT(2) receptors

作者：Miura Shin ichiro^*; Matsuo Yoshino; Kiya Yoshihiro; Karnik Sadashiva S; Saku Keijiro

来源：Biochemical and Biophysical Research Communications, 2010, 391(1): 85-90.

DOI：10.1016/j.bbrc.2009.11.008

• Angiotensin II receptors
• Signal cross-talk
• Dimerization
• Inositol phosphate production
• Phospholipase C

Although angiotensin II (Ang II) binds to Ang II type I (AT(1)) and type 2 (AT(2)) receptors. AT(1) and AT(2) receptors have antagonistic actions with regard to cell signaling. The molecular mechanisms that underlie this antagonism are not well understood. We examined AT(1) and AT(2) receptor-induced signal cross-talk in the cytoplasm and the importance of the hetero-dimerization of AT(1) receptor with AT(2) receptor on the cell surface. AT(1) and AT(2) receptors showed antagonistic effects toward inositol phosphate production AT(1) receptors mainly formed homo-dimers, rather than hetero-dimers with AT(2) receptor, on the cell surface as determined by immunoprecipitation, and subsequently induced cell signals AT(2) receptor mainly formed homo-dimers. rather than hetero-dimers with AT(1) receptor, on the cell surface. The expression levels of homo-dimerized AT(1) receptor or AT(2) receptor on the cell surface did not change after treatment with Ang II, the AT(1) receptor antagonist telmisartan or the AT(2) receptor antagonist PD123319 Finally, AT(1) and AT(2) receptor-induced signals antagonized phospholipase C-beta(3) phosphorylation in conclusion, Ang II-induced AT(1) receptor signals may be mainly blocked by AT(2) receptor signals through their negative cross-talk in the cytoplasm rather than by the hetero-dimerization of both receptors on the cell surface. The proper balance of the expression levels of AT(1) and AT(2) receptors might be critical for the antagonistic action between these receptors.

• 出版日期2010-1-1