Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Reprod Biomed Online ; 16(5): 705-11, 2008 May.
Article in English | MEDLINE | ID: mdl-18492376

ABSTRACT

Small human pre-antral follicles can be enzymatically isolated from the surrounding stroma, and are able to survive after 7 days of xenografting. The aim of the present study was to assess the developmental capacity of enzymatically isolated human follicles after long-term xenografting to severe combined immunodeficient (SCID) mice. Ovarian biopsies were obtained from three women 26-29 years of age. Human ovarian tissue was enzymatically dissociated using collagenase or a purified collagenase blend to obtain isolated follicles that were xenografted to SCID mice for 5 months. Recombinant FSH was given to the mice for the last 2 weeks. Five months after xenografting, follicular morphology was assessed by histology, and follicular proliferation by Ki-67 immunohistochemistry. Four grafts containing a total of 84 follicles were recovered. This follicular population was composed of 11 primordial follicles, 38 primary follicles, 31 secondary follicles and four antral follicles. Ki-67 was found to stain granulosa cells in antral follicles intensively. The results demonstrate, for the first time, that isolated human follicles are able to survive after long-term xenografting, and can develop into antral follicles after FSH stimulation.


Subject(s)
Ovarian Follicle/transplantation , Transplantation, Heterologous , Adult , Animals , Female , Follicle Stimulating Hormone/administration & dosage , Humans , Immunohistochemistry , Ki-67 Antigen/metabolism , Mice , Mice, SCID , Ovarian Follicle/metabolism , Recombinant Proteins/administration & dosage
2.
Reproduction ; 134(2): 253-62, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17660235

ABSTRACT

This study was designed to evaluate follicular survival and growth after short-term transplantation of fresh isolated human follicles and ovarian cortical tissue to nude mice. Ovarian biopsies were obtained from nine women undergoing laparoscopy. Twelve nude mice were xenografted with an ovarian cortical fragment in the right ovarian bursa, and a clot containing isolated follicles in the left, for a period of 7 days. One ungrafted fragment was used as a control. Histological sections were analyzed to determine follicle number and stage. The proliferative status of follicular cells was assessed by Ki-67 immunostaining. A total of 659 follicles was analyzed by histology and 545 follicles by immunohistochemistry. The percentage of primordial follicles was found to be markedly reduced 1 week post-grafting when compared with ungrafted tissue, while the percentage of primary follicles had significantly increased. Only 8% of follicles showed Ki-67-positive granulosa cells before grafting, whereas 1 week after grafting, 71% of follicles in fragments and 67% of isolated follicles were Ki-67-positive (P<0.001). Moreover, the histological aspect of isolated follicle grafts was similar to that of grafted fragments: follicles were surrounded by vimentin-positive stroma-like tissue of human origin, as confirmed by fluorescent in situ hybridization with human-specific probes. Our results demonstrate, for the first time, that isolated human follicles are able to survive and grow after xenografting. This study also shows massive in vivo follicular activation after transplantation of grafted fragments and isolated follicles. One week after grafting, well-structured stroma-like tissue of human origin was observed around the isolated follicles. The potential origin of this stroma is discussed.


Subject(s)
Mice, Nude , Ovarian Follicle/transplantation , Ovary/transplantation , Transplantation, Heterologous , Animals , Antibodies, Monoclonal , Biomarkers/analysis , Cell Proliferation , Female , Humans , Immunohistochemistry , In Situ Hybridization, Fluorescence , Mice , Ovarian Follicle/cytology , Ovarian Follicle/physiology , Ovary/cytology , Staining and Labeling , Stromal Cells/cytology , Tissue Culture Techniques , Vimentin
SELECTION OF CITATIONS
SEARCH DETAIL
...