TY - JOUR
T1 - Aberrant gonadotropin-releasing hormone receptor (GnRHR) expression and its regulation of CYP11B2 expression and aldosterone production in adrenal aldosterone-producing adenoma (APA)
AU - Nakamura, Yasuhiro
AU - Hattangady, Namita G.
AU - Ye, Ping
AU - Satoh, Fumitoshi
AU - Morimoto, Ryo
AU - Ito-Saito, Takako
AU - Sugawara, Akira
AU - Ohba, Koji
AU - Takahashi, Kazuhiro
AU - Rainey, William E.
AU - Sasano, Hironobu
PY - 2014/3/25
Y1 - 2014/3/25
N2 - Aberrant expression of gonadotropin-releasing hormone receptor (GnRHR) has been reported in human adrenal tissues including aldosterone-producing adenoma (APA). However, the details of its expression and functional role in adrenals are still not clear. In this study, quantitative RT-PCR analysis revealed the mean level of GnRHR mRNA was significantly higher in APAs than in human normal adrenal (NA) (P=0.004). GnRHR protein expression was detected in human NA and neoplastic adrenal tissues. In H295R cells transfected with GnRHR, treatment with GnRH resulted in a concentration-dependent increase in CYP11B2 reporter activity. Chronic activation of GnRHR with GnRH (100. nM), in a cell line with doxycycline-inducible GnRHR (H295R-TR/GnRHR), increased CYP11B2 expression and aldosterone production. These agonistic effects were inhibited by blockers for the calcium signaling pathway, KN93 and calmidazolium. These results suggest GnRH, through heterotopic expression of its receptor, may be a potential regulator of CYP11B2 expression levels in some cases of APA.
AB - Aberrant expression of gonadotropin-releasing hormone receptor (GnRHR) has been reported in human adrenal tissues including aldosterone-producing adenoma (APA). However, the details of its expression and functional role in adrenals are still not clear. In this study, quantitative RT-PCR analysis revealed the mean level of GnRHR mRNA was significantly higher in APAs than in human normal adrenal (NA) (P=0.004). GnRHR protein expression was detected in human NA and neoplastic adrenal tissues. In H295R cells transfected with GnRHR, treatment with GnRH resulted in a concentration-dependent increase in CYP11B2 reporter activity. Chronic activation of GnRHR with GnRH (100. nM), in a cell line with doxycycline-inducible GnRHR (H295R-TR/GnRHR), increased CYP11B2 expression and aldosterone production. These agonistic effects were inhibited by blockers for the calcium signaling pathway, KN93 and calmidazolium. These results suggest GnRH, through heterotopic expression of its receptor, may be a potential regulator of CYP11B2 expression levels in some cases of APA.
KW - Adrenal aldosterone-producing adenoma (APA)
KW - Aldosterone
KW - CYP11B2
KW - Gonadotropin-releasing hormone receptor (GnRHR)
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UR - http://www.scopus.com/inward/citedby.url?scp=84894082176&partnerID=8YFLogxK
U2 - 10.1016/j.mce.2014.01.016
DO - 10.1016/j.mce.2014.01.016
M3 - Article
C2 - 24472523
AN - SCOPUS:84894082176
SN - 0303-7207
VL - 384
SP - 102
EP - 108
JO - Molecular and Cellular Endocrinology
JF - Molecular and Cellular Endocrinology
IS - 1-2
ER -