In vivo imaging of physiological angiogenesis from immature to preovulatory ovarian follicles

To develop a model for the study of physiological angiogenesis, we transpla nted ovarian follicles onto striated muscle tissue and analyzed the process of microvascularization in vivo using repeated fluorescence microscopy. Fo llicles were mechanically isolated from unstimulated as well as pregnant ma re's serum gonadotropin (PMSG)- or PMSG/luteinizing hormone (LH)-stimulated Syrian golden hamster ovaries and were transplanted as free grafts into do rsal skinfold chambers of untreated or synchronized hamsters. Follicles lac king thecal cell layers did not vascularize regardless whether harvested fr om unstimulated or PMSG-stimulated animals, but underwent granulosa cell ap optosis, as indicated in vivo by nuclear condensation and fragmentation of bisbenzimide-stained follicular tissue. In contrast, all follicles at 48 ho urs after PMSG treatment with a multilayered thecal shell exhibited initial signs of angiogenesis within 3 days. Vascularization was completed within 7 to 10 days, comprising a dense glomerulum-like microvascular network. Nat ure and extent of vascularization of follicles harvested at 72 hours after either PMSG or PMSG/LH treatment did not notably differ from each other whe n transplanted into the respective synchronized animals. However, follicles with PMSG/LH treatment revealed significantly larger microvessel diameters and higher capillary blood perfusion compared to follicles with sole PMSG treatment, probably reflecting the adaptation to the increased functional d emand upon the LH surge. Using the unique experimental approach of ovarian follicle transplantation in the dorsal skinfold chamber of Syrian golden ha msters, we could show in vivo the developmental stage-dependent vasculariza tion of follicular grafts with sustained potential to meet their metabolic demand by increased blood perfusion.