Surrogate Mothers: IVF embryos transferred to another mother
Fertilization is a complex sequence of coordinated molecular events that starts with sperm-oocyte contact and ends with maternal and paternal chromosome mix at metaphase of 1st mitotic division of zygote, unicellular embryo, approximately 24hrs.
Capacitation involves the removal of a glycoprotein coat and seminal proteins from the sperm's acrosomal surface.
The cortical reaction prompts the release of cortical granules from the oocyte into the perivitelline space.
The contact between the sperm and the oocyte triggers the cortical reaction.
The acrosomal reaction involves the release of enzymes from the acrosome, aiding in the breakdown of the protective layers around the egg.
Sperm undergoing capacitation become more functionally active without significant morphological changes.
The acrosomal enzymes help in breaking down the proteins and glycoproteins within the zona pellucida.
Once a sperm penetrates through the zona pellucida, it enters the perivitelline space.
The change in resting membrane potential of the oocyte's plasma membrane prevents other sperm from binding and fusing with the oocyte.
The cortical reaction prevents polyspermy by modifying the zona pellucida and oocyte's membrane.
The binding of sperm to ZP-3 receptors triggers the acrosomal reaction.
The breakdown of the zona pellucida allows for the penetration of a single spermatozoon.
The site of fertilization is the ampulla of the uterine tube, a common site for fertilization due to its larger diameter and the presence of ciliated cells, aiding in the movement and guidance of the ovum.
After ovulation, the secondary oocyte is released from the ovary and swept into the infundibulum, which is the funnel-shaped part of the fallopian tube by the movement of fimbriae and fluid produced by ciliated cells.
The movement of the fimbriae, along with the ciliary action and the fluid secreted by the tubal epithelial cells, create a gentle current that assists in guiding the secondary oocyte into the infundibulum.
Spermatozoa are expelled from male genital duct through semen, introduced into the vagina through sexual intercourse, pass through the cervix uterine lumen, and reach the ampulla.
Spermatogenesis is the process by which male gametes (sperm) are produced from diploid stem cells called spermatogonia.
Spermatozoa are activated in the female reproductive tract, becoming more hyperactive and having a higher affinity to bind to zona pellucida receptors.
Capacitation is the alterations in the sperm's structure and functionality, leading to increased cAMP levels, enhanced tyrosine phosphorylation, and a rise in intracellular calcium levels within the sperm cells.
Approximately 30 hours post-fertilization, the zygote initiates its division into blastomeres.
The chromosomal sex of an embryo is determined by the kind of sperm that fertilizes it, with Sperm X leading to 46 XX and Sperm Y leading to 46 XY.
The series of mitotic divisions significantly increase the number of cells within the developing embryo.
While the number of cells increases, each individual cell, or blastomere, becomes progressively smaller with each division.
These divisions lead to the formation of cells called blastomeres.
Fluid begins to accumulate within the morula, creating a fluid-filled cavity called the blastocystic cavity.
As fluid continues to accumulate, it leads to the expansion of the blastocystic cavity, resulting in the separation and organization of blastomeres into two distinct parts.
Following the fusion of the male and female pronuclei, there is a breakdown of the membranes surrounding each pronucleus.
Following fertilization, the zygote begins a series of rapid cell divisions known as cleavage divisions.
These cells are pluripotent and give rise to the embryo itself, differentiating into the various cell types and tissues that form the organism.
Trophoblastic cells secrete early pregnancy factor, which appears in the maternal serum within 24 -48 h after fertilization and is the basis of pregnancy tests.
After a series of cell divisions, the blastomeres reach a stage where they align themselves tightly, a process known as compaction.
Variation in human species determines the chromosomal sex of the embryo and initiates cell division of the zygote.
The compacted ball of cells, following the process of compaction, progresses to form a structure known as the morula.
Compaction is a critical developmental event that transforms the aligned blastomeres into a tightly packed, compacted ball of cells.
The hatched blastocyst increases in size & nourished by uterine gland secretions.
Fertilization induces the oocyte to complete the second meiotic division and restores chromosome number (diploid, 2n, 46) in the zygote.
The trophoblast is essential for implantation and eventually gives rise to the embryonic part of the placenta and other extraembryonic structures necessary for supporting the developing embryo/fetus.
Compaction is essential for the segregation of cells within the morula that ultimately contribute to the formation of the inner cell mass (ICM) of the blastocyst.
Within the blastocyst, the inner cell mass (ICM) or embryoblast is a group of centrally located cells that remain clustered together.