We are slowly getting better at
all this. A chimera is a creature formed
from the cells of two separate individuals, in this case of the same
species. In folklore, it is extended to
include two separate species which we can not yet rule out.
I do not think that chimeras have
any real place in our future except in the odd sophisticated experiment.
Yet I have made the conjecture
that the cheetah was plausibly a created life form made by combining the
chromosomes of a cat and a dog into one creature. I do not expect this to actually stand up but
it remains untested. Two things suggest
the possibility. The chromosome count is
a simple addition of the cat and dog chromosome count itself. The second thing is that genetic work on the
cheetah shows us that the line went through a genetic crisis 40,000 years ago
in which only a few members existed.
That just happens to coincide
with the first rise of modernism among humanity on Earth and the first
establishment of the necessary ability.
It is reasonable that we could pull something like this of in the next
twenty years ourselves.
Those following my blog will know
that our present human world was kicked off with an agricultural base, around
ten thousand years ago after the Pleistocene Nonconformity of 12,900 years ago ended
the Ice Age and flooded out the continental shelf. The earlier rise of humanity established modernism
around 40,000BP and was responsible for the Pleistocene Nonconformity itself.
World’s First Primate Chimeric Offspring Produced: Research
Demonstrates Not All Embryonic Stem Cells Are Equal
ScienceDaily (Jan. 5, 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 is being 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.
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