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In biology, a blastomere is a type of cell produced by cell division (cleavage) of the zygote after fertilization; blastomeres are an essential part of blastula formation, and blastocyst formation in .
The blastomere is considered totipotent; that is, blastomeres are capable of developing from a single cell into a fully fertile adult organism. This has been demonstrated through studies and conjectures made with mouse blastomeres, which have been accepted as true for most mammalian blastomeres as well. Studies have analyzed monozygotic twin mouse blastomeres in their two-cell state, and have found that when one of the twin blastomeres is destroyed, a fully fertile adult mouse can still develop. Thus, it can be assumed that since one of the twin cells was totipotent, the destroyed one originally was as well.
Relative blastomere size within the embryo is dependent not only on the stage of the cleavage, but also on the regularity of the cleavage amongst the cells. If the number of blastomeres in the cellular mass is even, then the sizes of the cells should be congruent. However, if the number of blastomeres in the cellular mass is not even, then the division should be asynchronous such that the sizes of the cells best support the mass's specific stage of differentiation. Blastomere size is typically considered uneven when one blastomere has a diameter over 25% larger than that of the other being compared.
During the 8-cell differentiation period, the blastomeres form adheren junctions, and subsequently polarize along the apical-basal axis. This polarization permanently changes the morphology of these cells, and starts the differentiation process. After this, the 8-cell blastomere mass begins to compact by forming tight junctions between themselves, and cytosolic components of the cell accumulate in the apical region while the nucleus of each cell moves to the basal region. The adhesive lateral junction is then formed, and the blastomere is flattened to establish the apical cortical domain. Once the transition begins to a 16-cell mass, the apical cortical domain disappears, but elements of polarity are preserved. This allows for approximately half of the blastomeres to inherit polar regions that can rebuild the apical cortical domain. The other blastomeres that differentiate, then, will become apolar. Polar blastomere cells that differentiate will move to an outer position in the developing blastocyst and show precursors for the Trophoblast, while the apolar cells will move to an inner position and begin developing into the embryo. The cells will then fully commit to their individual states in one of these two domains at the 32-cell stage.
The other, more widely accepted model is known as the "cell-polarity model". This model states that the orientation of the cleavage plane at the 8-cell and 16-cell stages determines their later differentiation. There are two main ways in which blastomeres typically divide: symmetrically, meaning perpendicular to the apical-basal axis, or asymmetrically, meaning horizontal to the apical-basal axis. Many potential hypotheses and conjectures that attempt to explain why these cells orient themselves the way that they do. Some researchers have stated that early-dividing blastomeres tend to divide asymmetrically, while others have proposed that the orientation of 8-cell stage blastomeres is random and cannot be predicted on a larger scale. One study in particular states that the position of the nucleus in each blastomere can be used to indicate how the cell will divide: if the nucleus is in the apical region then the cell will likely divide symmetrically, while if the nucleus is located in the basal region then the cell will likely divide asymmetrically.
This mosaicism, especially of diploidy and polyploidy, can lead to the failure of cell cleavage and mitosis. When these necessary early cell divisions do not occur, the embryo can begin to form polyploid giant cancer cells that function very similarly to blastomere cells in order to grow and evolve in response to mechanical and chemical signals just like blastocyst precursors do. Studies have shown that these giant cancer cells are often also the genetic equivalent to somatic blastomeres.
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