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This is an accepted version of this page This is the latest accepted revision, reviewed on 26 January 2025. Cell division producing haploid gametes For the figure of speech, see Meiosis (figure of speech). For the process whereby cell nuclei divide to produce two copies of themselves, see Mitosis. For excessive constriction of the pupils, see Miosis. For the parasitic infestation, see Myiasis ...
Degenerated oocytes are classified as damaged oocytes or oocytes without a zona pellucida. [6] Dysmorphic oocytes are oocytes with abnormal physical characteristics, for example multiple nuclei. [7] EFS is a condition occurring when no oocytes are produced from the mature follicle after ovulation is induced in cycles of in vitro fertilisation ...
By definition it means, to recapitulate mammalian oogenesis and producing fertilizable oocytes in vitro.it is a complex process involving several different cell types, precise follicular cell-oocyte reciprocal interactions, a variety of nutrients and combinations of cytokines, and precise growth factors and hormones depending on the ...
Sperm entry causes calcium release into the oocyte. In mammals, this is caused by the introduction of phospholipase C isoform zeta (PLCζ) from the sperm cytoplasm. [1] Activation of the ovum includes the following events: Cortical reaction to block against other sperm cells; Activation of egg metabolism; Reactivation of meiosis; DNA synthesis
At birth, meiosis arrests at the diplotene phase of prophase I. [7] Oocytes will remain in this state until the time of puberty. At the time of ovulation a surge of LH initiates the resumption of meiosis and oocytes enter the second cycle, which is known as oocyte maturation. Meiosis is then arrested again during metaphase 2 until fertilisation ...
Oocytes are substantially larger than the average somatic cell, and thus considerable metabolic activity is necessary for their provisioning. If this metabolic activity were carried out by the oocyte's metabolic machinery, the oocyte genome would be exposed to the reactive oxidative by-products generated.
In the tertiary follicle, the basic structure of the mature follicle has formed and no novel cells are detectable. Granulosa and theca cells continue to undergo mitotis concomitant with an increase in antrum volume. Tertiary follicles can attain a tremendous size that is hampered only by the availability of FSH, which it is now dependent on.
Vitellogenesis is the process of yolk protein formation in the oocytes during sexual maturation. [2] The term vitellogenesis comes from the Latin vitellus ("egg yolk"). Yolk proteins, such as Lipovitellin and Phosvitin, provides maturing oocytes with the metabolic energy required for development.