LONDON: Scientists have created sperm cells from small pieces of ear tissue to help genetically infertile male mice produce healthy offspring, an advance that may pave the way for novel therapies to treat human infertility.
Our sex is determined by the X and Y chromosomes, researchers said. Usually, females have two X chromosomes (XX) and males have one X and one Y (XY), but about one in 500 men are born with an extra X or Y.
Having three rather than two sex chromosomes can disrupt formation of mature sperm and cause infertility.
In a study published in the journal Science, researchers at the Francis Crick Institute in the UK have found a way to remove the extra sex chromosome to produce fertile offspring.
If the findings can be safely transferred into humans, it might eventually be possible for men with Klinefelter syndrome (XXY) or Double Y syndrome (XYY) that are infertile to have children through assisted reproduction using this technique.
The team took small pieces of ear tissue from XXY and XYY mice, cultured them and collected connective tissue cells known as fibroblasts.
They turned the fibroblasts into stem cells and noticed that in the process, some of the cells lost the extra sex chromosome.
With an existing method, they used specific chemical signals to ‘guide’ the stem cells into becoming cells that have the potential to become sperm. These cells developed into mature sperm when injected into the testes of a host mouse.
The researchers then harvested these mature sperm and used them through assisted reproduction to create healthy, fertile offspring.
“Our approach allowed us to create offspring from sterile XXY and XYY mice,” said Takayuki Hirota from the Francis Crick Institute.
“It would be interesting to see whether the same approach could one day be used as a fertility treatment for men with three sex chromosomes,” said Hirota.
In a preliminary experiment, the team found that stem cells produced from fibroblasts of men with Klinefelter syndrome also lost the extra sex chromosome.
“There is currently no way to make mature sperm outside of the body. In our mouse experiments we have to inject cells that have the potential to become sperm back into the testes to help them finish developing,” said James Turner, Group Leader at the Francis Crick Institute.
“But we found that this caused tumours in some of the mouse recipients. So reducing the risk of tumour formation or discovering a way to produce mature sperm in a test tube will have to be developed before we can even consider this in humans,” said Turner. (AGENCIES)
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