Survival of human pre-antral follicles after cryopreservation of ovarian tissue, follicular isolation and in vitro culture in a calcium alginate matrix
Human Reproduction, 2009•academic.oup.com
BACKGROUND Ovarian tissue cryopreservation is a promising technique to safeguard
fertility in cancer patients. However, in some types of cancer, there is a risk of transmitting
malignant cells present in the cryopreserved tissue. To avoid such a risk, pre-antral follicles
could be isolated from ovarian tissue and grown in vitro. On the basis of this assumption, the
aim of our study was to investigate in vitro survival and growth of pre-antral follicles after
cryopreservation of ovarian tissue and follicular isolation, followed by encapsulation in …
fertility in cancer patients. However, in some types of cancer, there is a risk of transmitting
malignant cells present in the cryopreserved tissue. To avoid such a risk, pre-antral follicles
could be isolated from ovarian tissue and grown in vitro. On the basis of this assumption, the
aim of our study was to investigate in vitro survival and growth of pre-antral follicles after
cryopreservation of ovarian tissue and follicular isolation, followed by encapsulation in …
BACKGROUND
Ovarian tissue cryopreservation is a promising technique to safeguard fertility in cancer patients. However, in some types of cancer, there is a risk of transmitting malignant cells present in the cryopreserved tissue. To avoid such a risk, pre-antral follicles could be isolated from ovarian tissue and grown in vitro. On the basis of this assumption, the aim of our study was to investigate in vitro survival and growth of pre-antral follicles after cryopreservation of ovarian tissue and follicular isolation, followed by encapsulation in alginate beads.
METHODS
Ovarian biopsies from four patients were frozen and thawed. Pre-antral follicles were then isolated and embedded in an alginate matrix before in vitro culture for 7 days.
RESULTS
Small pre-antral follicles (42.98 ± 9.06 µm) from frozen–thawed tissue can survive and develop after enzymatic isolation and in vitro culture. A total of 159 follicles were incubated in a three-dimensional system (alginate hydrogel) and, after 7 days, all of them showed an increase in size (final size 56.73 ± 13.10 µm). The survival rate of the follicles was 90% (oocyte and all granulosa cells viable).
CONCLUSION
Our preliminary results indicate that alginate hydrogels may be a suitable system for in vitro culture of isolated human pre-antral follicles. However, more studies are required to establish whether follicular morphology and functionality can be maintained using this matrix.
Oxford University Press