Messenger RNA expression and protein localization of growth hormone in bovine ovarian tissue and in cumulus oocyte complexes (COCs) during in vitro maturation
F. Izadyar et al., Messenger RNA expression and protein localization of growth hormone in bovine ovarian tissue and in cumulus oocyte complexes (COCs) during in vitro maturation, MOL REPROD, 53(4), 1999, pp. 398-406
The aim of this study was to investigate whether bovine cumulus oocyte comp
lexes (COCs) obtained from 2 to 8 mm follicles synthesize growth hormone (G
H) during in vitro maturation. In addition the expression of growth hormone
releasing hormone receptor (GHRH-r) in the COCs before and after in vitro
maturation was investigated. Therefore, COCs obtained from small and medium
sized follicles were cultured in M199 supplemented with 10% FCS and gonado
tropins for 24 hr. At 0, 6, 12, and 24 hr after the onset of culture, COCs
were removed and were prepared for immunohistochemical staining to detect t
he presence of GH. In addition, sections of ovary were stained to study the
differential localization of GH in the ovary. At 0 and 24 hr COCs were rem
oved and together with samples from granulosa cells and theca cells were pr
epared for reverse transcriptase polymerase chain reaction (RT-PCR) to asse
ss the expression of mRNA of GH and GHRH-r. Within COCs, cumulus cells and
oocytes showed GH immunoreactivity, while expression of GH mRNA was only fo
und in the oocyte. At the onset of culture, oocytes and cumulus cells in th
e majority of COCs generally showed moderate and strong staining intensity
for GH, respectively. While GH staining in the cumulus cells did hardly cha
nge during 24 hr of culture, GH staining in the oocyte was absent after 24
hr of culture in 70% of COCs. Within the ovary, GH was localized in antral
follicles larger than 2 mm and no staining was found in primordial, primary
and secondary follicles or in the stroma. The intensity of the staining in
creased with the size of the follicles. Within the follicular wall the GH w
as persistently observed in granulosa cells, while theca cells were occasio
nally negative. GH mRNA in follicular compartments was only found in the oo
cyte and mural granulosa cells. No GHRH-r mRNA was found in the COCs nor in
the granulosa or the stroma. In conclusion, the gradual increase of GH sta
ining during follicular development and the consistent synthesis of GH in o
ocytes and granulosa cells, suggest a paracrine and/or autocrine action for
GH in bovine follicular growth and oocyte maturation. The absence of mRNA
for GHRH receptor in the COCs indicates that ovarian production of GH is no
t regulated by GHRH. (C) 1999 Wiley-Liss, Inc.