Washington: Researchers have found a way to turn skin cells into embryonic stem cells, which could lead to the creation of a complete embryo from skin cells.
The research conducted on mice has significant implications for modelling embryonic disease and placental dysfunctions. The study was published in Cell Stem Cell.
Dr Yossi Buganim and his team discovered a set of genes capable of transforming murine skin cells into all three cell types that comprise the early embryo: the embryo itself, the placenta and the extra-embryonic tissues, such as the umbilical cord.
In the future, it may be possible to create entire human embryos out of human skin cells, without the need for sperm or eggs. This discovery also has vast implications for modelling embryonic defects and shedding light on placental dysfunctions, as well as solving certain infertility problems by creating human embryos in a petri dish.
Back in 2006, Japanese researchers discovered the capacity of skin cells to be “reprogrammed” into early embryonic cells that can generate an entire foetus, by expressing four central embryonic genes.
These reprogrammed skin cells, termed “Induced Pluripotent Stem Cells” (iPSCs), are similar to cells that develop in the early days after fertilization and are essentially identical to their natural counterparts. These cells can develop into all foetal cell types, but not into extra-embryonic tissues, such as the placenta.
Now, the Hebrew University research team, headed by Dr Yossi Buganim, Dr Oren Ram from the HU’s Institute of Life Science and Professor Tommy Kaplan from HU’s School of Computer Science and Engineering, as well as doctoral students Hani Benchetrit and Mohammad Jaber, found a new combination of five genes that, when inserted into skin cells, reprogram the cells into each of the three early embryonic cell types — iPS cells which create foetuses, placental stem cells, and stem cells that develop into other extra-embryonic tissues, such as the umbilical cord. These transformations take about one month.
The HU team used new technology to scrutinise the molecular forces that govern cell fate decisions for skin cell reprogramming and the natural process of embryonic development.
For example, the researchers discovered that the gene “Eomes” pushes the cell towards placental stem cell identity and placental development, while the “Esrrb” gene orchestrates foetus stem cells development through the temporary acquisition of an extra-embryonic stem cell identity.
To uncover the molecular mechanisms that are activated during the formation of these various cell types, the researchers analysed changes to the genome structure and function inside the cells when the five genes are introduced into the cell.
They discovered that during the first stage, skin cells lose their cellular identity and then slowly acquire a new identity of one of the three early embryonic cell types and that this process is governed by the levels of two of the five genes.
Recently, attempts have been made to develop an entire mouse embryo without using sperm or egg cells. These attempts used the three early cell types isolated directly from a live, developing embryo.
However, HU’s study is the first attempt to create all three main cell lineages at once from skin cells. Further, these findings mean there may be no need to “sacrifice” a live embryo to create a test tube embryo.
[source_without_link]ANI[/source_without_link]