C. Graveleau et al., Presence of a 5-HT7 receptor positively coupled to adenylate cyclase activation in human granulosa-lutein cells, J CLIN END, 85(3), 2000, pp. 1277-1286
Although serotonin (5-HT) has been shown to stimulate progesterone producti
on by human granulosa-lutein cells (hGLC), the receptor type and associated
signaling pathway remain uncharacterized. We report here that 5-HT recepto
rs in these cells are positively coupled to adenylate cyclase activity. For
mation of cAMP was stimulated by 5-HT and its agonists in a dose- and time-
dependent manner. Mianserin, amoxapine, and loxapine were equipotent in ant
agonizing 5-HT-induced cAMP formation. For both cAMP formation in cells and
adenylate cyclase assay using membrane fractions, the rank order of potenc
y for agonists of 5-HT were: 5-carboxy-aminotryptamine >5-HT> or =5-methoxy
tryptamine, consistent with a typical kpharmacological profile of human 5-h
t(7) (h5-ht(7)) receptor. Sequence data of amplified complementary DNA frag
ments reverse transcribed from hGLC RNA revealed complete identity with pub
lished sequence of h5-ht(7) receptor complementary DNA. Northern analysis s
howed the presence of 2.8-kb h5-ht(7) transcripts in hGLC. The three varian
ts h5-ht(7A) h5-ht(7B), and h5-ht(7D) were also detected in hGLC. Preincuba
tion of hGLC with 5-HT (10(-8)-10(-6) M) resulted in a marked reduction in
the cAMP response when the cells were subsequently stimulated with gonadotr
opin, and this heterologous desensitization could be reversed by 5-ht(7) re
ceptor antagonist clozapine. These data demonstrate that h5-ht(7) receptor
is present and stimulate cAMP formation in hGLC. In addition, the h5-ht(7)
receptor seems to be implicated in the heterologous down-regulation hCG-sti
mulated cAMP response in hGLC, with a possible ramification for luteal insu
fficiency.