2001
DOI: 10.1093/humrep/16.4.737
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Effects of low O2 and ageing on spindles and chromosomes in mouse oocytes from pre-antral follicle culture

Abstract: To assess their quality, spindles were analysed in mouse oocytes from pre-antral follicle culture. High or low oxygen tension was present during the last 16 or 20 h post human chorionic gonadotrophin (HCG)/epidermal growth factor (EGF) addition. Most oocytes from pre-antral follicle culture possessed typical anastral spindles with flat poles resembling those of ovulated, in-vivo-matured oocytes of sexually mature mice, while denuded oocytes in-vitro matured to metaphase II (MII) formed significantly longer, sl… Show more

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Cited by 100 publications
(63 citation statements)
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“…Both increased FSH dose and higher serum peak estradiol levels were associated with the lack of spindle detection with the PolScope. Although, increased FSH stimulation Several investigators have reported that the meiotic spindle is a dynamic structure and that various environm e n t a l c o n d i t i o n s c a n p r o d u c e t e m p o r a r y depolymerisation without the occurrence of a real impairment of oocyte quality [16][17][18]. This depolymerisation may be caused by changes in culture conditions such as temperature and pH.…”
Section: Discussionmentioning
confidence: 99%
“…Both increased FSH dose and higher serum peak estradiol levels were associated with the lack of spindle detection with the PolScope. Although, increased FSH stimulation Several investigators have reported that the meiotic spindle is a dynamic structure and that various environm e n t a l c o n d i t i o n s c a n p r o d u c e t e m p o r a r y depolymerisation without the occurrence of a real impairment of oocyte quality [16][17][18]. This depolymerisation may be caused by changes in culture conditions such as temperature and pH.…”
Section: Discussionmentioning
confidence: 99%
“…Since the 1970s, the study of oxygen concentration during mouse oocyte maturation has almost exclusively involved the use of 5 or 20% oxygen mixtures (Eppig and Wigglesworth, 1995;Hu et al, 2001;Adam, 2004). This is largely due to previous studies showing that a 5% oxygen concentration is optimal for oocyte nuclear maturation (as measured by extrusion of a polar body) in both mouse and hamster (Haidri et al, 1971;Gwatkin and Haidri, 1974) and that mouse embryo culture is widely performed under 5% O 2 (Harlow and Quinn, 1979).…”
Section: Discussionmentioning
confidence: 99%
“…For example, although murine ovarian tissue is exposed to plasma oxygen levels of about 5% in vivo, mouse follicles grown in vitro in 5% oxygen had a higher frequency of mature oocytes with incorrectly aligned chromosomes and many died prematurely when compared with follicles cultured in 20% oxygen (Hu et al 2001). Similarly, sheep follicles grown in 5% oxygen had reduced antral cavity formation and increased lactate and glucose consumption when grown under hypoxic conditions of 5% oxygen relative to sized matched counterparts that were grown in 20% oxygen .…”
Section: The Follicle Culture Environment In Vitromentioning
confidence: 99%