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Biology of Reproduction, Vol 23, 545-552, Copyright © 1980 by Society for the Study of Reproduction
1 The Jackson Laboratory,
Bar Harbor, Maine 04609 In previous studies it was shown that highly purified follicle stimulating hormone (FSH), but
not highly purified luteinizing hormone (LH) or human chorionic gonadotropin (hCG), stimulated
hyaluronic acid synthesis and cumulus expansion in vitro by cumuli oophori isolated from mice
primed with pregnant mare serum gonadotropin (PMSG). In contrast, it is shown here that highly
purified hCG stimulated hyaluronic acid synthesis, cumulus expansion, and ovulation when injected into PMSG-primed mice. Cumulus expansion was also stimulated by hCG in ovarian organ
cultures. Therefore, the action of injected hCG was probably directly on ovarian constituents.
Culture of cumuli oophori in medium containing hCG was not effective in completing the cumulus
expansion-stimulating processes begun by hCG in vivo. Therefore, the cumuli do not acquire the
ability to respond directly to hCG in vitro as a result of the injection of hCG in vivo. This result
also suggests that cumuli oophori do not respond directly to hCG in vivo. Preparations of crude
follicular fluid (CFF) from PMSG-primed mice were very active in stimulating hyaluronic acid
synthesis and cumulus expansion by isolated cumuli oophori. This showed that CFF contained
both FSH-like activity that stimulated hyaluronic acid synthesis and the serum-like factor(s)
necessary for the retention of the hyaluronic acid within the oocyte-cumulus cell complexes.
PMSG stimulated the expansion of cultured cumuli oophori isolated from PMSG-primed mice and
from mice not primed with PMSG. However, the PMSG priming itself did not stimulate cumulus
expansion in vivo. Therefore, ample cumulus expansion-stimulating activity was potentially available to the oocyte-cumulus cell complexes in vivo as a result of PMSG-priming and in the follicular
fluid, but the cumulus cells did not respond to this activity until after the hCG injection. Taken
together, the results of these experiments suggest that hCG stimulates cumulus expansion in vivo
by an indirect mechanism. It is hypothesized that some component(s) of the intact Graafian
follicles prevents the response of the cumuli oophori to the FSH-like activity present in the follicle
until that inhibition is terminated as a result of hCG administration or the endogenous LH surge.
Note:
ACKNOWLEDGMENTS
This research was supported by a grant from NSF
(PCM79-10618). I thank Cindy Grindle and Avis
Silva for their excellent assistance in this research. I
am grateful to Dr. A. F. Parlow and the Rat Pituitary
Distribution Program of the NIAMDD and R. E.
Canfield and the Center for Population Research of
the NICHHD for generously providing the gonadotropins. The Jackson Laboratory is fully accredited by
the American Association for Accreditation of Laboratory Animal Care.
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