Shoukhrat Mitalipov,
OHSU: First successful birth of chimeric monkeys achieved
January 06, 2012
Newly
published research by scientists at Oregon Health & Science University
provides significant new information about how early embryonic stem
cells develop and take part in formation of the primate species. The
research, which took place at OHSU’s Oregon National Primate Research
Center, has also resulted in the first successful birth of chimeric
monkeys -- monkeys developed from stem cells taken from two separate
embryos. The research will be published this week in the online edition
of the journal Cell and will be published in a future printed copy of
the journal.
The research was conducted to gain a better understanding of the
differences between natural stem cells residing in early embryos and
their cultured counterparts called embryonic stem cells. This study also
determined that stem cell functions and abilities are different between
primates and rodents.
Here’s more information about the early primate stem cells that were
studied: The first cell type was totipotent cells – cells from the early
embryo that have the ability to divide and produce all of the
differentiated cells in the placenta and the body of organism. These
were compared with pluripotent cells – cells derived from the later
stage embryo that have only the ability to become the body but not
placenta.
In
mice, either totipotent or pluripotent cells from two different animals
can be combined to transform into an embryo that later becomes a
chimeric animal. However, the current research demonstrated that for
reasons yet unknown, chimeric animals can only develop from totipotent
cells in a higher animal model: the rhesus macaque. OHSU showed this to
be the case by successfully producing the world's first primate chimeric
offspring, three baby rhesus macaques named Roku, Hex and Chimero.
“This
is an important development - not because anyone would develop human
chimeras - but because it points out a key distinction between species
and between different kind of stem cells that will impact our
understanding of stem cells and their future potential in regenerative
medicine," explained Shoukhrat Mitalipov, Ph.D., an associate scientist
in the Division of Reproductive and Developmental Sciences at ONPRC.
“Stem cell therapies hold great promise for replacing damaged nerve
cells in those who have been paralyzed due to a spinal cord injury or
for example, in replacing dopamine-producing cells in Parkinson’s
patients who lose these brain cells resulting in disease. As we move
stem cell therapies from the lab to clinics and from the mouse to
humans, we need to understand what these cells do and what they can’t do
and also how cell function can differ in species.”
The OHSU Oregon National Primate Research Center and the National
Institutes of Health funded the research.