Scientists have discovered a process that could transform human organ transplants
Hundreds of people die every day while waiting for an organ
transplant. A solution to this horrible reality is to make human organs
readily available—by growing them on-demand in labs or even other
animals.
Scientists in Japan and the US have taken a huge step in that direction. In a study published in Nature, they report to have cured mice of diabetes by transplanting mouse cells grown in rats.
To achieve this feat, researchers injected mouse pluripotent stem
cells into a rat embryo. As the name suggests, these pluripotent stem
cells are able to transform themselves into all types of cells. The
mouse cells intermingled with rat cells, and created a chimera whose
organs and tissues were almost all created from a mix of mouse and rat
cells.
Crucially, however, they had modified the rat to not produce pancreatic cells. They achieved this by knocking out a gene called Pdx1. The upshot was that the pancreas in the chimera was almost completely made of mouse cells.
When
the rat-mouse chimeras became adults, the researchers removed the
animals’ pancreases and from them, isolated endocrine islets, which
contain β-cells that produce insulin. The β-cells were then transplanted
to diabetic mice that had lost all their native β-cells.
Every human-to-human organ transplant requires the use of drugs that
suppress the immune system. Though these drugs have severe side effects,
without them, the body would consider the transplanted object foreign
and unleash the immune system on it. Often a transplant patient has to
take these drugs for life.
Anticipating a similar reaction, the mice that received the
transplant were put on mild immunosuppressant drugs. However, the
scientists found they only needed to administer the drugs for five days
after transplantation. Surprisingly, the few rat cells that came along
during the transplant (mostly in the blood vessels in the islets) had
been destroyed and replaced by the mouse’s own cells.
Scientists don’t know yet how this happened. Qiao Zhou of Harvard University, who was not involved in the research, thinks that one way
this could have occurred is that, despite the mild immunosuppressant
drugs, the mouse’s immune system recognized the few rat cells present in
the transplantation, and destroyed them. At the same time, native mouse
cells started building blood vessels to replace them.
The β-cells in mice that got the transplants functioned just as they
would in a healthy mouse for more than a year, which was the complete
observation period. These lab mice only live for two to three years,
which makes a one-year observation fairly long. The research opens up
the door for growing human organs inside, say, a pig, using the
patient’s own stem cells and then transplanting the organ when it’s
mature and ready.
There are, of course, many obstacles before we achieve that feat. For
instance, the pancreas is a relatively uncomplicated organ, genetically
speaking. Scientists only had to knock out one gene to ensure that rat
cells didn’t participate in creating the organ and mouse cells could
monopolize the construction. Creation of more complex organs like the
heart or kidney are controlled by many more genes, which often have
multiple purposes in the body, and thus will require a more complicated
genetic modification technique—or some other workaround to ensure that
the changes made won’t destroy some other part of the body.
In addition, mice and rats, though separate species, are close
cousins. Transplanting from a pig to a human would be a bigger leap, and
it will come with its own challenges. (Pigs have some organs that are
roughly the same size as humans, which is why they are good candidates
for future organ transplant techniques).
And maybe we won’t even have to do all that. Researchers are also
trying a different tack: xenotransplantations, where organs from a
different species are used without the need to create a chimera. In
2013, researchers at Northwestern University showed that endocrine
islets from rats could survive and thrive in mice without the use of immunosuppressant drugs.
ANAΔΗΜΟΣΙΕΥΣΗ ΑΠΟ ΤΟ FUTURESCOPE.COM 26/1/2017
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