Abstract During the last decade, new technologies in reproductive medicine have emerged to preserve the fertility of women whose gonadal function is threatened by premature menopause or gonadotoxic treatments. To offer an individualized approach to these patients, different experimental procedures are under investigation, including oocyte cryopreservation and cryopreservation and transplantation of ovarian tissue in the form of cortical fragments, whole ovary or isolated follicles. This review shows that transmission electron microscopy (TEM), combined with other in-vivo and in-vitro analysis techniques, is a valuable tool in the establishment of new experimental protocols to preserve female fertility. Ultrastructural studies allow in-depth evaluation of the oocyte's unique morpho-functional characteristics, which explain its low cryotolerance, and provide essential information on follicular, stromal and endothelial cell integrity, as well as cellular interactions crucial for normal folliculogenesis. In order to be able to offer appropriate and efficient options in every clinical situation, oocyte in-vitro maturation and ovarian tissue transplantation need to be optimized. Further development of new approaches, such as follicular isolation and whole ovary transplantation, should be encouraged. Fine ultrastructural details highlighted by TEM studies will be useful for the further optimization of these emerging technologies.

Preservation of fertility in young cancer patients: contribution of transmission electron microscopy / Alessandra, Camboni; Belen Martinez, Madrid; Marie Madeleine, Dolmans; Christiani Andrade, Amorim; Nottola, Stefania Annarita; Jacques, Donnez; Anne Van, Langendonckt. - In: REPRODUCTIVE BIOMEDICINE ONLINE. - ISSN 1472-6483. - STAMPA. - 17:1(2008), pp. 136-150. [10.1016/s1472-6483(10)60303-3]

Preservation of fertility in young cancer patients: contribution of transmission electron microscopy

NOTTOLA, Stefania Annarita;
2008

Abstract

Abstract During the last decade, new technologies in reproductive medicine have emerged to preserve the fertility of women whose gonadal function is threatened by premature menopause or gonadotoxic treatments. To offer an individualized approach to these patients, different experimental procedures are under investigation, including oocyte cryopreservation and cryopreservation and transplantation of ovarian tissue in the form of cortical fragments, whole ovary or isolated follicles. This review shows that transmission electron microscopy (TEM), combined with other in-vivo and in-vitro analysis techniques, is a valuable tool in the establishment of new experimental protocols to preserve female fertility. Ultrastructural studies allow in-depth evaluation of the oocyte's unique morpho-functional characteristics, which explain its low cryotolerance, and provide essential information on follicular, stromal and endothelial cell integrity, as well as cellular interactions crucial for normal folliculogenesis. In order to be able to offer appropriate and efficient options in every clinical situation, oocyte in-vitro maturation and ovarian tissue transplantation need to be optimized. Further development of new approaches, such as follicular isolation and whole ovary transplantation, should be encouraged. Fine ultrastructural details highlighted by TEM studies will be useful for the further optimization of these emerging technologies.
2008
fertility preservation; oocyte; ovarian tissue; transmission electron microscopy; transplantation
01 Pubblicazione su rivista::01a Articolo in rivista
Preservation of fertility in young cancer patients: contribution of transmission electron microscopy / Alessandra, Camboni; Belen Martinez, Madrid; Marie Madeleine, Dolmans; Christiani Andrade, Amorim; Nottola, Stefania Annarita; Jacques, Donnez; Anne Van, Langendonckt. - In: REPRODUCTIVE BIOMEDICINE ONLINE. - ISSN 1472-6483. - STAMPA. - 17:1(2008), pp. 136-150. [10.1016/s1472-6483(10)60303-3]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/40168
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