One out of every six Canadian couples experiences infertility. Some resort to in vitro fertilization. But the embryos obtained through this technique often have defects. In a study published in the journal Current Biology, researchers succeeded in reducing the number of defects in mouse embryos in the laboratory. In the medium term, this unprecedented discovery could improve infertile couples' chances of giving birth.
About half of the embryos generated during in vitro fertilization fertility treatments contain cells with an abnormal number of chromosomes. This abnormality, called aneuploidy, is well known in reproductive biology and is considered a major cause of infertility.
In most cells, chromosome segregation error is averted by the spindle assembly checkpoint (SAC), which prevents anaphase-promoting complex (APC/C) activation and anaphase onset until chromosomes are aligned with kinetochores attached to spindle microtubules, but little is known about the SAC’s role in the early mammalian embryo.
"In our study, we explain at least one of the reasons why this occurs. We found that it's due to a defect in a mechanism called the "spindle checkpoint." We also show that if we manipulate this checkpoint in mouse embryos by using a simple drug, we can reduce the chances of error by about half," explained the senior author.
Authors show that misaligned chromosomes in the early mouse embryo can recruit SAC components to mount a checkpoint signal, but this signal fails to prevent anaphase onset, leading to high levels of chromosome segregation error. They find that failure of the SAC to prolong mitosis is not attributable to cell size.
By administering the right dose of this synthetic substance called proTAME, researchers observed that a larger percentage of cells of each of the mouse embryos had a normal number of chromosomes. In mice, a normal oocyte (ovum) contains 20 chromosomes, whereas in humans it contains 23. proTAME inhibition of APC/C can extend mitosis, thereby allowing more time for correct chromosome alignment and reducing segregation errors. SACAPC/C disconnect thus presents a mechanistic explanation for frequent chromosome segregation errors in early mammalian embryos.
Making the best possible embryo is one of the keys to success when it comes to in vitro fertilization. This discovery is still at the basic research stage, being conducted in the laboratory on mice. It's very important to be cautious about its application to humans.
"The potential for transferring the technique to humans is clear. And I'm sure that fertility clinics would really like to try it in the hope of creating 'better embryos.' However, it would be very irresponsible to implement this concept clinically at this point, before safety tests have been successfully carried out," emphasized the researcher.
https://www.cell.com/current-biology/fulltext/S0960-9822(18)31676-2
Preventing chromosome segregation errors in embryo
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