AT1 AND GPER-1 HETERODIMERIZATION POTENTIATES CYP11B2 GENE EXPRESSION IN ALDOSTERONE PRODUCING ADENOMA. (June 2018)
- Record Type:
- Journal Article
- Title:
- AT1 AND GPER-1 HETERODIMERIZATION POTENTIATES CYP11B2 GENE EXPRESSION IN ALDOSTERONE PRODUCING ADENOMA. (June 2018)
- Main Title:
- AT1 AND GPER-1 HETERODIMERIZATION POTENTIATES CYP11B2 GENE EXPRESSION IN ALDOSTERONE PRODUCING ADENOMA
- Authors:
- Piazza, M.
Caroccia, B.
Seccia, T.M.
Pivato, L.
Rossi, G.P. - Abstract:
- Abstract : Objective: Aldosterone producing adenomas (APAs) exhibit increased expression levels of G protein-coupled receptors (GPCRs), including the GPCRs Angiotensin (Ang) II type 1 receptor (AT1R) and G protein-coupled estrogen receptor-1 (GPER-1), which trigger aldosterone production by binding Ang II and 17B-estradiol or aldosterone. Since a functional crosstalk between GPCRs has been reported, we investigated if AT1R and GPER-1 crosstalk to activate CYP11B2 gene expression in APA Design and method: APA strips and adrenocortical carcinoma cell line HAC15 were exposed to [100 nM] aldosterone alone or in presence of [100 nM] Ang II for 12 hours, and/or after pre-treatment with the selective AT1R antagonist irbesartan and/or the selective GPER-1 antagonist G36. The experimental end-point was CYP11B2 gene expression change. HAC15 proteins were immunoprecipitated with an antibody for AT1R, and GPER-1 expression was revealed by immunoblot in immunoprecipitated proteins. Results: In APA strips both aldosterone and Ang II increased CYP11B2 gene expression (+220% and + 190%, respectively, p < 0.01 vs untreated); aldosterone on top of Ang II potentiated the secretagogue effect of Ang II (+400%, p < 0.001 vs untreated). The synergistic effect of aldosterone and Ang II was inhibited by either irbesartan or G36. Similarly, in HAC15 cells aldosterone potentiated the effect of Ang II (+800% vs Ang II alone; + 1300% vs aldosterone alone), and pre-treatment with irbesartan and/or G36Abstract : Objective: Aldosterone producing adenomas (APAs) exhibit increased expression levels of G protein-coupled receptors (GPCRs), including the GPCRs Angiotensin (Ang) II type 1 receptor (AT1R) and G protein-coupled estrogen receptor-1 (GPER-1), which trigger aldosterone production by binding Ang II and 17B-estradiol or aldosterone. Since a functional crosstalk between GPCRs has been reported, we investigated if AT1R and GPER-1 crosstalk to activate CYP11B2 gene expression in APA Design and method: APA strips and adrenocortical carcinoma cell line HAC15 were exposed to [100 nM] aldosterone alone or in presence of [100 nM] Ang II for 12 hours, and/or after pre-treatment with the selective AT1R antagonist irbesartan and/or the selective GPER-1 antagonist G36. The experimental end-point was CYP11B2 gene expression change. HAC15 proteins were immunoprecipitated with an antibody for AT1R, and GPER-1 expression was revealed by immunoblot in immunoprecipitated proteins. Results: In APA strips both aldosterone and Ang II increased CYP11B2 gene expression (+220% and + 190%, respectively, p < 0.01 vs untreated); aldosterone on top of Ang II potentiated the secretagogue effect of Ang II (+400%, p < 0.001 vs untreated). The synergistic effect of aldosterone and Ang II was inhibited by either irbesartan or G36. Similarly, in HAC15 cells aldosterone potentiated the effect of Ang II (+800% vs Ang II alone; + 1300% vs aldosterone alone), and pre-treatment with irbesartan and/or G36 blunted the synergistic effect of aldosterone plus Ang II. After immunoprecipitation for AT1R, GPER-1 protein expression was detected by immunoblot Conclusions: Aldosterone and Ang II can increase the expression of CYP11B2 through a crosstalk between GPER-1 and AT1R receptors. In HAC15 cells AT1R and GPER-1 form heterodimers which interact to induce an autonomous aldosterone production in APAs. … (more)
- Is Part Of:
- Journal of hypertension. Volume 36(2018)Supplement 1
- Journal:
- Journal of hypertension
- Issue:
- Volume 36(2018)Supplement 1
- Issue Display:
- Volume 36, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 36
- Issue:
- 1
- Issue Sort Value:
- 2018-0036-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2018-06
- Subjects:
- Hypertension -- Periodicals
Hypertension -- Periodicals
616.132005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://journals.lww.com/jhypertension/pages/default.aspx ↗
http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00004872-000000000-00000 ↗
http://www.jhypertension.com/ ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/01.hjh.0000539187.92708.24 ↗
- Languages:
- English
- ISSNs:
- 1473-5598
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5004.510000
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