PMID- 15353131 OWN - NLM STAT- MEDLINE DCOM- 20050329 LR - 20141120 IS - 1001-0602 (Print) IS - 1001-0602 (Linking) VI - 14 IP - 4 DP - 2004 Aug TI - Apoptosis in granulosa cells during follicular atresia: relationship with steroids and insulin-like growth factors. PG - 341-6 AB - It is well known that during mammalian ovarian follicular development, the majority of follicles undergo atresia at various stages of their development. However, the mechanisms controlling this selection process remain unknown. In this study, we investigated apoptosis in granulosa cells during goat follicular atresia by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL). The changes in the levels of steroids, insulin-like growth factors (IGFs) and IGF receptors were studied by radioimmunoassay (RIA) and semi-quantitative reverse transcription-PCR. We found that the percentage of apoptotic granulosa cells in the atretic (A) follicles was significantly higher than that in the slightly atretic (SA) and healthy (H) follicles. The level of estradiol and the ratio of estradiol to progesterone in H follicles were significantly higher than those in A follicles. On the other hand, the level of progesterone was not significantly different among these follicle types. We also found that the level of IGF-I in H follicles was higher than in SA and A follicles, whereas the amount of IGF-II did not vary significantly. The expression of IGF receptor also decreased in A follicles as compared to that in H and SA follicles. These results suggested that estradiol and IGF-I might be involved in controlling apoptosis in granulosa cells during follicular atresia. FAU - Yu, Yuan Song AU - Yu YS AD - Laboratory of Animal Reproduction and Embryology College of Animal Sciences and Veterinary Medicine, Shandong Agricultural University, Taian, Shandong 271018, China. FAU - Sui, Hong Shu AU - Sui HS FAU - Han, Zheng Bin AU - Han ZB FAU - Li, Wei AU - Li W FAU - Luo, Ming Jiu AU - Luo MJ FAU - Tan, Jing He AU - Tan JH LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Cell Res JT - Cell research JID - 9425763 RN - 0 (Estrogens) RN - 0 (Somatomedins) RN - 0 (Steroids) RN - 3XMK78S47O (Testosterone) RN - 4G7DS2Q64Y (Progesterone) RN - 67763-96-6 (Insulin-Like Growth Factor I) RN - 67763-97-7 (Insulin-Like Growth Factor II) RN - EC 2.7.10.1 (Receptor, IGF Type 1) SB - IM MH - Animals MH - Apoptosis/*physiology MH - Estrogens/metabolism MH - Female MH - Follicular Atresia/*physiology MH - Follicular Fluid/metabolism MH - Goats MH - Granulosa Cells/cytology/*metabolism MH - In Situ Nick-End Labeling MH - In Vitro Techniques MH - Insulin-Like Growth Factor I/metabolism MH - Insulin-Like Growth Factor II/metabolism MH - Ovarian Follicle/cytology/*metabolism MH - Progesterone/metabolism MH - Radioimmunoassay MH - Receptor, IGF Type 1/metabolism MH - Somatomedins/*metabolism MH - Steroids/*metabolism MH - Testosterone/metabolism EDAT- 2004/09/09 05:00 MHDA- 2005/03/30 09:00 CRDT- 2004/09/09 05:00 PHST- 2004/09/09 05:00 [pubmed] PHST- 2005/03/30 09:00 [medline] PHST- 2004/09/09 05:00 [entrez] AID - 10.1038/sj.cr.7290234 [doi] PST - ppublish SO - Cell Res. 2004 Aug;14(4):341-6. doi: 10.1038/sj.cr.7290234.