4.3 Article

Dynamic medium containing growth differentiation factor-9 and FSH maintains survival and promotes in vitro growth of caprine preantral follicles after long-term in vitro culture

Journal

REPRODUCTION FERTILITY AND DEVELOPMENT
Volume 25, Issue 6, Pages 955-965

Publisher

CSIRO PUBLISHING
DOI: 10.1071/RD12180

Keywords

folliculogenesis; goat; hormone; ovary

Funding

  1. National Council for Scientific and Technological Development (CNPq)
  2. Coordination for Improvement of Graduate Personnel (CAPES)
  3. Brazilian Innovation Agency (FINEP)
  4. Ceara State Foundation for the Support of Scientific and Technological Development (FUNCAP)

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The aim of the present study was to evaluate the effects of growth differentiation factor 9 (GDF-9) and FSH on the in vitro development of caprine preantral follicles cultured for 16 days. Ovarian fragments were cultured in alpha MEM+ (alpha-minimum essential medium, pH 7.2-7.4, 10 mu g mL(-1) insulin, 5.5 mu g mL(-1) transferrin, 5.0 ng mL(-1) selenium, 2 mM glutamine, 2 mM hypoxanthine and 1.25 mg mL(-1) bovine serum albumin) in the absence or presence of 200 ng mL(-1) GDF-9 and/or 50 ng mL(-1) FSH added during the first (Days 0-8) and/or second (Days 8-16) half of the culture period. Non-cultured and cultured fragments were processed for histological and ultrastructural analyses. After 16 days, all treatments using GDF-9 or FSH showed higher rates of follicular survival compared with alpha MEM+ alone. Compared with non-cultured control, sequential culture media containing GDF-9 and/or FSH significantly increased the percentage of developing follicles and follicle diameter. Moreover, a progressive increase in oocyte diameter was observed only with sequential culture medium containing GDF-9 until Day 8 followed by FSH (GDF-9/FSH) in the second half of the culture period. After 16 days of culture, ultrastructural analysis confirmed the integrity of follicles cultured in the presence of GDF-9/FSH. In conclusion, a dynamic medium containing GDF-9 and FSH (GDF-9/FSH) maintained follicular integrity and promoted activation of primordial follicles and growth during long-term in vitro culture of goat preantral follicles.

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