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Vasoactive intestinal peptide promotes differentiation and clock gene expression in granulosa cells from prehierarchal follicles
Author(s) -
Kim Dongwon,
Johnson Alan L.
Publication year - 2016
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/mrd.22641
Subject(s) - biology , vasoactive intestinal peptide , endocrinology , medicine , granulosa cell , ovarian follicle , follicle stimulating hormone receptor , follicle , cyclic adenosine monophosphate , microbiology and biotechnology , receptor , ovary , follicle stimulating hormone , hormone , neuropeptide , luteinizing hormone , genetics
SUMMARY Vasoactive intestinal peptide (VIP) signaling via cyclic adenosine monophosphate (cAMP) is reported to stimulate steroidogenesis in ovarian granulosa cells from a variety of vertebrate species, including the domestic hen. Prior to follicle selection in the hen ovary (i.e., cyclic recruitment) follicle‐stimulating‐hormone (FSH)‐induced cAMP signaling is absent within the granulosa layer until immediately following follicle selection. As a consequence, granulosa cells remain in an undifferentiated state and are unable to initiate FSH‐induced steroidogenesis. VIP receptors (VPAC1 and VPAC2), like the FSH receptor, are G protein‐coupled receptors, so we predicted that VIP signaling in granulosa cells is also absent in follicles that have not yet been selected into the preovulatory hierarchy. Initial studies established that mRNA encoding VPAC1 and VPAC2 are expressed within the granulosa cells throughout follicle development. Nevertheless, undifferentiated granulosa cells from prehierarchal (6–8 mm) follicles do not accumulate cAMP in response to a 4‐hr incubation with chicken VIP; the capacity for such receptor signaling is attained only following selection within actively differentiating granulosa cells. VIP treatment did, however, increase expression of mRNA encoding the Gallus circadian clock protein, BMAL1—but only in granulosa cells collected from selected follicles. These findings provide evidence that, at follicle selection, the acquisition of VIP‐induced cAMP cell signaling helps initiate and promote the differentiation of of granulosa cells. Furthermore, we propose that VIP signaling may regulate BMAL1 expression and, thus, a daily rhythmicity within granulosa cells of preovulatory follicles. Mol. Reprod. Dev. 83: 455–463, 2016. © 2016 Wiley Periodicals, Inc .