OBJECTIVE: A number of hormones and growth factors have been reported to affect the in vitro maturation of oocytes. Their exact effects on follicular growth and oocyte maturation and the mechanisms involved are still unclear. In the present study, we have investigated the effects of Growth Hormone (GH) and Insulin-like Growth Factor 1 (IGF-1) on the in vitro maturation of mouse oocytes. DESIGN: Immature preovulatory oocytes without cumulus cells (denuded), were obtained from 4- to 8-week old female mice and were cultured in Ham's F-10 medium. GH and IGF-1 were added separately or in combination in gradually increasing concentrations in the culture media, while medium-only containing samples were employed as controls. Oocyte development was assessed daily for three days and maturation was considered to be completed when the first polar body appeared. RESULTS: In control samples, 44+/-3% (mean+/-SE) of denuded oocytes formed a polar body. The achieved maturation rate after the addition of either GH or IGF-1 or GH plus IGF-1 was significantly higher than in controls. The highest maturation rates were achieved after the addition of 0.2 microg/ml GH (76%+/-5%), 50 ng/ml IGF-1 (69%+/-5%) and a combination of 0.2 microg/ml GH plus 10 ng/ml IGF-1 (75%+/-5%). CONCLUSIONS: The data suggest that GH and IGF-1, alone or in combination, affect mouse oocyte maturation significantly. The lack of a synergistic effect on oocyte cultures when both hormones were added indicates that both hormones act through the same signaling pathway.
OBJECTIVE: A number of hormones and growth factors have been reported to affect the in vitro maturation of oocytes. Their exact effects on follicular growth and oocyte maturation and the mechanisms involved are still unclear. In the present study, we have investigated the effects of Growth Hormone (GH) and Insulin-like Growth Factor 1 (IGF-1) on the in vitro maturation of mouse oocytes. DESIGN: Immature preovulatory oocytes without cumulus cells (denuded), were obtained from 4- to 8-week old female mice and were cultured in Ham's F-10 medium. GH and IGF-1 were added separately or in combination in gradually increasing concentrations in the culture media, while medium-only containing samples were employed as controls. Oocyte development was assessed daily for three days and maturation was considered to be completed when the first polar body appeared. RESULTS: In control samples, 44+/-3% (mean+/-SE) of denuded oocytes formed a polar body. The achieved maturation rate after the addition of either GH or IGF-1 or GH plus IGF-1 was significantly higher than in controls. The highest maturation rates were achieved after the addition of 0.2 microg/ml GH (76%+/-5%), 50 ng/ml IGF-1 (69%+/-5%) and a combination of 0.2 microg/ml GH plus 10 ng/ml IGF-1 (75%+/-5%). CONCLUSIONS: The data suggest that GH and IGF-1, alone or in combination, affect mouse oocyte maturation significantly. The lack of a synergistic effect on oocyte cultures when both hormones were added indicates that both hormones act through the same signaling pathway.
Authors: Ye Yuan; Lee D Spate; Bethany K Redel; Yuchen Tian; Jie Zhou; Randall S Prather; R Michael Roberts Journal: Proc Natl Acad Sci U S A Date: 2017-07-03 Impact factor: 11.205