Just a few years ago, we thought that brains were all about
neurons. Sure, we also have glial cells,
but the job of the lowly glia is to take care of the neurons, which do all the
serious cognitive work.
But why are the glia of humans and other primates
so large and varied in their shape and structure? Why are they so different from the simpler,
smaller glia found in mice and other rodents?
Could the difference play a role in the evolution of human intelligence?
One way to compare a mouse and a human is to create
a mouse that is part human. That’s
exactly what researchers at the University of Rochester did. They implanted human cells into mouse
brains. More precisely, they implanted
human glial progenitor cells into newborn mouse pups.
What they got were chimeras, mice with human cells integrated into their brains. When the researchers examined the brains of these chimeric mice, they found that the human cells proliferated and were widely present throughout the brain. Although interacting with mouse brain cells, the human cells remained distinctly human in their unusually large size and varied structures.
Photo credit: A 23 week human culture astrocyte stained for GFAP. From Wikimedia Commons. Date: 24 February 2012. Author: Bruno Pascal.
Most surprising is that
the chimeric mice were smarter than unaltered mice born in the same
litters. Human glia in a mouse brain
seems to make a smarter mouse.
Why? The answer probably involves one type of glial cell called astrocytes. Compared to other species, human brains have
many more astrocytes. Ours are larger and
more varied in their structure, capable of connecting many neurons and
coordinating the activity that occurs at many synapses.
Based on this study, published in the March 7, 2013 issue
of Cell Stem Cell, we now know that human astrocytes boost intelligence in
chimeric mice as measured by standard testing procedures.
This is pretty good evidence to suggest that the
evolution of the larger, more complex glial cells was a critical aspect of the
evolution of higher intelligence. At
least that is the conclusion drawn by one of the senior authors of the paper, Steven
Goldman. “In a fundamental sense are we different from lower species,” he said,
according to a press release from the University of Rochester. “Our advanced
cognitive processing capabilities exist not only because of the size and
complexity of our neural networks, but also because of the increase in
functional capabilities and coordination afforded by human glia.”
What makes this study intriguing is that it uses
stem cell technology to study brain function and to learn something important
about evolution. By implanting stem
cells in create chimeric mice, researchers learn that glia play a critically
important role in intelligence and that evolved changes in glial cells are a
key part of the story of the rise of intelligence.
Concerning the role of glial cells in the complex
brain, Maiken Nedergaard, another senior author, had this to say:
“I have always found the concept that the human brain is more capable
because we have more complex neural networks to be a little too simple, because
if you put the entire neural network and all of its activity together all you
just end up with a super computer.”
“But human cognition is far more than just
processing data, it is also comprised of the coordination of emotion with
memory that informs our higher abilities to abstract and learn,” Nedergaard
added.
And concerning what chimeric mice have to teach us
about evolution, Steven Goldman made this comment: “This study indicates that
glia are not only essential to neural transmission, but also suggest that the
development of human cognition may reflect the evolution of human-specific
glial form and function.”
Or to quote the original paper: “These observations
strongly support the notion that the evolution of human neural processing, and
hence the species-specific aspects of human cognition, in part may reflect the
course of astrocytic evolution.”
The paper does not address the interesting ethical
questions raised by making smarter mice.
Over the past decade, ethicists have debated the moral legitimacy of
chimeric animals. One point of concern
has been the creation of nonhuman animals with human brain cells. To defend this practice, it is often said
that a mouse brain with human cells is still a mouse brain. It still has the structure or architecture of
a mouse brain. It may have human cells,
but in no way is it a human brain or even a half mouse/half human brain.
This study suggests we should take a closer look at
that line of thinking. Maybe it is true
that adding human neurons to a mouse brain does not change the mouse brain
structure. But this study implies that
adding human astrocytes to a mouse brain may begin some small but significant
change in structure and function.
The study is clear about the fact these chimeric
mice are more intelligent than the unmodified mice. Their brains are quite literally
faster.
Once again, Goldman: “The bottom line is that these
mice demonstrated an increase in plasticity and learning within their existing
neural networks, essentially changing their functional capabilities.”
These animals have been cognitively “elevated,” to
use a word sometimes found in the debate.
Probably no one will object to the idea of a slightly smarter
mouse. Researchers take special care to
make sure these mice do not breed and produce pups of their own. But even if they did, the added intelligence
would not pass to future generations.
They would produce normal lab mice.
Even so, this study—combining stem cells
technology, neuroscience, and evolution in one elegant package—raises intriguing
moral questions. Are we smart enough to
know how far we should go in creating smarter mice?
The study, entitled “Forebrain engraftment by human glialprogenitor cells enhances synaptic plasticity and learning in adult mice,”
appears in the March 7, 2013 issue of Cell Stem Cell.
1 comment:
Especially the biology revolution, it is defined as any genetic change in a population that is inherited over several generations. Some changes during the process can occur through a mutation. Can the mouse indicate some functions of BKV (capsid protein VP2)?
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