Abstract

BackgroundIn vitro maturation of ovarian follicles, in combination with cryopreservation, might be a valuable method for preserving and/or restoring fertility in mammals with impaired reproductive function. Several culture systems capable of sustaining mammalian follicle growth in vitro have been developed and many studies exist on factors influencing the development of in vitro grown oocytes. However, a very few reports concern the ultrastructural morphology of in vitro grown follicles.MethodsThe present study was designed to evaluate, by transmission and scanning electron microscopy, the ultrastructural features of isolated mouse preantral follicles cultured in vitro for 6 days in a standard medium containing fetal calf serum (FCS). The culture was supplemented or not with FSH.ResultsThe follicles cultured in FCS alone, without FSH supplementation (FCS follicles), did not form the antral cavity. They displayed low differentiation (juxta-nuclear aggregates of organelles in the ooplasm, a variable amount of microvilli on the oolemma, numerous granulosa cell-oolemma contacts, signs of degeneration in granulosa cell compartment). Eighty (80)% of FSH-treated follicles formed the antral cavity (FSH antral follicles). These follicles showed various ultrastructural markers of maturity (spreading of organelles in ooplasm, abundant microvilli on the oolemma, scarce granulosa cell-oolemma contacts, granulosa cell proliferation). Areas of detachment of the innermost granulosa cell layer from the oocyte were also found, along with a diffuse granulosa cell loosening compatible with the antral formation. Theca cells showed an immature morphology for the stage reached. Twenty (20)% of FSH-treated follicles did not develop the antral cavity (FSH non-antral follicles) and displayed morphological differentiation features intermediate between those shown by FCS and FSH antral follicles (spreading of organelles in the ooplasm, variable amount of microvilli, scattered granulosa cell-oolemma contacts, signs of degeneration in granulosa cell compartment).ConclusionsIt is concluded that FSH supports the in vitro growth of follicles, but the presence of a diffuse structural granulosa cell-oocyte uncoupling and the absence of theca development unveil the incomplete efficiency of the system. The present study contributes to explain, from a morphological point of view, the effects of culture conditions on the development of mouse in vitro grown follicles and to highlight the necessity of maintaining efficient intercellular communications to obtain large numbers of fully-grown mature germ cells.

Highlights

  • In vitro maturation of ovarian follicles, in combination with cryopreservation, might be a valuable method for preserving and/or restoring fertility in mammals with impaired reproductive function

  • By phase contrast microscopy (PCM) the antral cavity (AC) appeared as a translucent area in the GC mass that could comprise about half of the follicle

  • 10 follicles from each group were prepared for light microscopy (LM)-transmission electron microscopy (TEM) analysis whereas the remaining follicles were destined to scanning electron microscopy (SEM) examination

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Summary

Introduction

In vitro maturation of ovarian follicles, in combination with cryopreservation, might be a valuable method for preserving and/or restoring fertility in mammals with impaired reproductive function. In vitro culture and maturation of preantral ovarian follicles currently represents one of the most important tools of investigation in the field of assisted reproduction This technique, in combination with cryopreservation, might be a valuable method for preserving and/or tissue and to subject them to subsequent in vitro culture [2,8,9,10,11,12,13,14,15,16]. Numerous in vitro culture systems for ovarian mammalian follicles and immature oocytes have been designed to study regulative processes occurring during folliculogenesis and oogenesis These studies contributed to the development of new reproductive biotechnologies, including clinical application in the treatment of human infertility [1,15,17,18,19,20,21,22]. This is partially due to the heterogeneity of the follicle population present in the adult ovarian tissue and to the extreme variability of culture systems and media, including considerable variations in length of the culture period in relation to different animal species [1,18,23]

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