Researchers at the Hebrew University of
Jerusalem (HU) have found a way to transform skin cells into the three
major stem cell types that comprise early-stage embryos. The work (in
mouse cells) has significant implications for modelling embryonic
disease and placental dysfunctions, as well as paving the way to create
whole embryos from skin cells.
As published in Cell Stem Cell, Dr. Yossi Buganim of HU's
Department of Developmental Biology and Cancer Research and his team
discovered a set of genes capable of transforming murine skin cells into
all three of the 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 fetus, by expressing four central embryonic genes. These
reprogrammed skin cells, termed "Induced Plutipotent 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 fetal 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 three early embryonic cell
types -- iPS cells which create fetuses, 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 scrutinize 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 fetus stem cells development through the temporary
acquisition of an extrae-mbryonic stem cell identity.
To uncover the molecular mechanisms that are activated during the
formation of these various cell types, the researchers analyzed 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.
Journal Reference:
- Hana Benchetrit, Mohammad Jaber, Valery Zayat, Shulamit Sebban, Avital Pushett, Kirill Makedonski, Zvi Zakheim, Ahmed Radwan, Noam Maoz, Rachel Lasry, Noa Renous, Michal Inbar, Oren Ram, Tommy Kaplan, Yosef Buganim. Direct Induction of the Three Pre-implantation Blastocyst Cell Types from Fibroblasts. Cell Stem Cell, 2019; DOI: 10.1016/j.stem.2019.03.018
Courtesy: ScienceDaily
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