Steady-state level of insulin-like growth factor-I (IGF-I) receptor mRNA and the effect of IGF-I on the in vitro culture of caprine preantral follicles

被引:34
作者
Magalhaes-Padilha, D. M. [1 ]
Duarte, A. B. G. [1 ]
Araujo, V. R. [1 ]
Saraiva, M. V. A. [1 ]
Almeida, A. P. [1 ]
Rodrigues, G. Q. [1 ]
Matos, M. H. T. [2 ]
Campello, C. C. [1 ]
Silva, J. R. [3 ]
Gastal, M. O. [4 ]
Gastal, E. L. [4 ]
Figueiredo, J. R. [1 ]
机构
[1] Univ Estadual Ceara, Fac Vet, Lab Manipulat Oocytes Enclosed Preantral Follicle, BR-60740000 Fortaleza, Ceara, Brazil
[2] Fed Univ Sao Francisco Valley, Nucleus Biotechnol Appl Ovarian Follicle Dev, BR-56300900 Petrolina, PE, Brazil
[3] Univ Fed Ceara, Biotecnol Nucleus Sobral NUBIS, BR-62042280 Sobral, CE, Brazil
[4] So Illinois Univ, Dept Anim Sci Food & Nutr, Carbondale, IL 62901 USA
关键词
Preantral follicle; In vitro development; IGF-I; IGFR; Ovary; Goat; LONG-TERM CULTURE; FOLLICULAR DEVELOPMENT; PRIMORDIAL FOLLICLES; STIMULATING-HORMONE; OOCYTES; LOCALIZATION; COMPETENCE; EXPRESSION; MATURATION; IMPROVES;
D O I
10.1016/j.theriogenology.2011.07.036
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The objectives were to quantify insulin-like growth factor receptor-1 (IGFR-1) mRNA in preantral follicles on Days 0 and 18 of in vitro culture in the presence or absence of FSH, and to evaluate the effects of IGF-I on the rate of normal follicles, antral cavity formation, and in vitro growth and maturation of caprine oocytes on Days 0, 6, 12, and 18 of culture. The expression of IGFR-1 was analyzed using real-time RT-PCR before and after follicle culture. Preantral follicles were isolated from the cortex of caprine ovaries and individually cultured for 18 d in the presence or absence of bovine IGF-I (50 or 100 ng/mL). At the end of the culture period, the oocytes were submitted to IVM. The expression of IGFR-1 mRNA in preantral follicles cultured in vitro only approached being significantly higher in follicles supplemented with FSH when compared to follicles immediately after recovery (P < 0.06) and cultured without FSH (P < 0.1). There was a higher (P < 0.05) percentage of normal follicles on Days 6, 12, and 18 of culture in IGF-I 50 (97, 92, 67%, respectively) and IGF-I 100 (100, 90, 80%) groups versus the control (90, 64, 36%). In addition, the rate of antrum formation at 6 and 12 d of culture was higher (P < 0.05) in IGF-I groups (IGF-I 50: 72 and 90% and IGF-I 100: 69 and 85%) than the control group (41 and 59%). After 18 d of culture, the percentages of grown oocytes acceptable for IVM were higher (P < 0.05) in follicles cultured in the presence of IGF-I (82 vs 49%). Furthermore, follicles cultured in the presence of IGF-I 50 and IGF-I 100 had higher (P < 0.05) meiotic resumption rates (63 and 66%, respectively) than the control group (11%). In conclusion, treatment with FSH tended to increase IGFR-1 mRNA expression during the in vitro culture of preantral follicles and the addition of IGF-I to the culture medium clearly improved the in vitro development of caprine preantral follicles. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:206 / 213
页数:8
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