Scientists have made ordinary human skin cells take on the
chameleon-like powers of embryonic stem cells, a startling
breakthrough that might someday deliver the medical payoffs of
embryo cloning without the controversy.
Laboratory teams on two continents report success in a pair of
landmark papers released Tuesday. It's a neck-and-neck finish to a
race that made headlines five months ago, when scientists announced
that the feat had been accomplished in mice.
The "direct reprogramming" technique avoids the swarm of
ethical, political and practical obstacles that have stymied
attempts to produce human stem cells by cloning embryos.
Researchers James Thomson
(L) and Junying Yu with the University of Wisconsin-Madison are
shown here in University of Wisconsin-Madison photographs. Yu is
lead author of a paper describing a novel method of reprogramming
adult stem cells to create cells that are indistinguishable from
embryonic stem cells. Researchers reported on November 20, 2007.
(agencies via China Daily)
Scientists familiar with the work said scientific questions
remain and that it's still important to pursue the cloning
strategy, but that the new work is a major coup.
"This work represents a tremendous scientific milestone -- the
biological equivalent of the Wright Brothers' first airplane," said
Dr. Robert Lanza, chief science officer of Advanced Cell
Technology, which has been trying to extract stem cells from cloned
human embryos.
"It's a bit like learning how to turn lead into gold," said
Lanza, while cautioning that the work is far from providing medical
payoffs.
"It's a huge deal," agreed Rudolf Jaenisch, a prominent stem
cell scientist at the Whitehead Institute in Cambridge, Mass. "You
have the proof of principle that you can do it."
There is a catch. At this point, the technique requires
disrupting the DNA of the skin cells, which creates the potential
for developing cancer. So it would be unacceptable for the most
touted use of embryonic cells: creating transplant tissue that in
theory could be used to treat diseases like diabetes, Parkinson's,
and spinal cord injury.
But the DNA disruption is just a byproduct of the technique, and
experts said they believe it can be avoided.
A scientific team from the University of
Wisconsin-Madison created genetic modifications in skin cells,
pictured here, to induce the cells into what scientists call a
pluripotent state - a condition that is essentially the same as
that of embryonic stem cells. Researchers reported on November 20,
2007, that they have transformed ordinary human skin cells into
batches of cells that look and act like embryonic stem cells -- but
without using cloning technology and without making embryos.
(photo: agencies via China Daily)
The new work is being published online by two
journals, Cell and Science. The Cell paper is from a team led by
Dr. Shinya Yamanaka of Kyoto University; the Science paper is from
a team led by Junying Yu, working in the lab of in stem-cell
pioneer James Thomson of the University of Wisconsin-Madison.
Both reported creating cells that behaved like stem cells in a
series of lab tests.
Thomson, 48, made headlines in 1998 when he announced that his
team had isolated human embryonic stem cells.
Yamanaka gained scientific notice in 2006 by reporting that
direct reprogramming in mice had produced cells resembling
embryonic stem cells, although with significant differences. In
June, his group and two others announced they'd created mouse cells
that were virtually indistinguishable from stem cells.
For the new work, the two men chose different cell types from a
tissue supplier. Yamanaka reprogrammed skin cells from the face of
an unidentified 36-year-old woman, and Thomson's team worked with
foreskin cells from a newborn. Thomson, who was working his way
from embryonic to fetal to adult cells, said he's still analyzing
his results with adult cells.
Both labs did basically the same thing. Each used viruses to
ferry four genes into the skin cells. These particular genes were
known to turn other genes on and off, but just how they produced
cells that mimic embryonic stem cells is a mystery.
"People didn't know it would be this easy," Thomson said.
"Thousands of labs in the United States can do this, basically
tomorrow."
The Wisconsin Alumni Research Foundation, which holds three
patents for Thomson's work, is applying for patents involving his
new research, a spokeswoman said. Two of the four genes he used
were different from Yamanaka's recipe.
Scientists prize embryonic stem cells because they can turn into
virtually any kind of cell in the body. The cloning approach --
which has worked so far only in mice and monkeys -- should be able
to produce stem cells that genetically match the person who donates
body cells for cloning.
That means tissue made from the cells should be transplantable
into that person without fear of rejection. Scientists emphasize
that any such payoff would be well in the future, and that the more
immediate medical benefits would come from basic research in the
lab.
In fact, many scientists say the cloning technique has proven
too expensive and cumbersome in its current form to produce stem
cells routinely for transplants.
The new work shows that the direct reprogramming technique can
also produce versatile cells that are genetically matched to a
person. But it avoids several problems that have bedeviled the
cloning approach.
For one thing, it doesn't require a supply of unfertilized human
eggs, which are hard to obtain for research and subjects the women
donating them to a surgical procedure. Using eggs also raises the
ethical questions of whether women should be paid for them.
In cloning, those eggs are used to make embryos from which stem
cells are harvested. But that destroys the embryos, which has led
to political opposition from President Bush, the Roman Catholic
church and others.
Those were "show-stopping ethical problems," said Laurie Zoloth,
director of Northwestern University's Center for Bioethics, Science
and Society.
The new work, she said, "redefines the ethical terrain."
Richard Doerflinger, deputy director of pro-life activities for
the US Conference of Catholic Bishops, called the new work "a very
significant breakthrough in finding morally unproblematic
alternatives to cloning. ... I think this is something that would
be readily acceptable to Catholics."
Another advantage of direct reprogramming is that it would
qualify for federal research funding, unlike projects that seek to
extract stem cells from human embryos, noted Doug Melton,
co-director of the Harvard Stem Cell Institute.
Still, scientific questions remain about the cells produced by
direct reprogramming, called "iPS" cells. One is how the cells
compare to embryonic stem cells in their behavior and potential.
Yamanaka said his work detected differences in gene activity.
If they're different, iPS cells might prove better for some
scientific uses and cloned stem cells preferable for other uses.
Scientists want to study the roots of genetic disease and screen
potential drug treatments in their laboratories, for example.
Scottish researcher Ian Wilmut, famous for his role in cloning
Dolly the sheep a decade ago, told London's Daily
Telegraph that he is giving up the cloning approach to produce
stem cells and plans to pursue direct reprogramming instead.
Other scientists said it's too early for the field to follow
Wilmut's lead. Cloning embryos to produce stem cells remains too
valuable as a research tool, Jaenisch said.
Dr. George Daley of the Harvard institute, who said his own lab
has also achieved direct reprogramming of human cells, said it's
not clear how long it will take to get around the cancer risk
problem. Nor is it clear just how direct reprogramming works, or
whether that approach mimics what happens in cloning, he noted.
So the cloning approach still has much to offer, he said.
Daley, who's president of the International Society for Stem
Cell Research, said his lab is pursuing both strategies.
"We'll see, ultimately, which one works and which one is more
practical."
(Agencies via China Daily November 21, 2007)