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UCLA researchers reprogram normal tissue cells into embryonic stem cells
June 07, 2007New technique could allow for cell reprogramming without use of controversial cloning methods
Researchers at the Institute for Stem Cell Biology and Medicine at UCLA were able to take normal tissue cells and reprogram them into cells with the same unlimited properties as embryonic stem cells, the cells that are able to give rise to every cell type found in the body.
The work, done in mouse models, appears in the inaugural June 7, 2007 issue of Cell Stem Cell, published by Cell Press. UCLA researchers, working closely with stem cell scientists at Harvard, took mouse fibroblasts, cells that develop into connective tissue, and added four transcription factors that bind to special sites on the DNA. Using this process, they were able to turn the fibroblasts into pluripotent cells that, in every aspect tested, were identical to embryonic stem cells.
The implications for disease treatment could be staggering. Reprogramming adult stem cells into embryonic stem cells could generate a potentially limitless source of immune-compatible cells for tissue engineering and transplantation medicine. If the work can be replicated in human cells, it may mean that a patient's skin cells, for example, could be reprogrammed to become embryonic stem cells. Those embryonic stem cells could then be prodded into becoming various cells types - beta islet cells to treat diabetes, hematopoetic cells to create a new blood supply for a leukemia patient, motor neuron cells to treat Parkinson's disease.
"If we can recreate this in human cells, it has significant implications for regenerative therapies," said Kathrin Plath, an assistant professor of biological chemistry, a researcher with the Institute for Stem Cell Biology and Medicine at UCLA (ISCBM) and co-lead author of the study. "Our reprogrammed cells were virtually indistinguishable from embryonic stem cells. We could find no evidence that they were different in any way. We were rather surprised at how well this reprogramming worked."
The finding also is significant in that this new technique could potentially replace a controversial method used to reprogram cells, somatic cell nuclear transfer (SCNT), sometimes referred to "therapeutic cloning." To date, SCNT has not been done successfully in human cells.
"If we can successfully reprogram a normal human cell into a cell with almost identical properties to those in embryonic stem cells without SCNT, it may have important therapeutic ramifications and provide us with another method to develop human stem cell lines," said Dr. Owen Witte, ISCBM director and a Howard Hughes Medical Institute investigator. "Up until now, it's been unclear whether a cell could be reprogrammed back into an embryonic stem cell state without the use of SCNT, so that makes this a very important finding."
Studies published previously had shown that the four transcription factors, which regulate expression of downstream genes and either activate or silence their expression, could reprogram cells into cells with some pluripotent properties. But they differed from embryonic stem cells in that they could not differentiate into every cell type or support development of adult tissues.
"They had very limited developmental potential," Plath said. "We took a different approach, carefully selecting from our pool of cells the reprogrammed cells that highly expressed two genes we know are essential in embryonic stem cells."
Selecting cells that highly expressed the genes, Oct4 and Nanog, essential to giving embryonic stem cells their unique characteristics resulted in reprogrammed cells with much more powerful pluripotency, Plath said.
The reprogrammed cells were not just functionally identical to embryonic stem cells. They also had identical biological structure. In a cell nucleus, DNA - an organism's unique map or instructions - wraps around histones, which serve as a kind of scaffolding for compaction of the long DNA molecule. Histones don't merely package DNA. Chemical tags on histones determine which genes are expressed or shut off in the DNA. In the reprogrammed cells, the location of the chemical tags along the DNA chromosomes were identical to those found in embryonic stem cells and, just as importantly, dramatically different from those in the fibroblasts before reprogramming. The structure of the reprogrammed cells - down to the very small chemical tags that dictate gene expression - is highly similar to that of embryonic stem cells.
Plath and her colleagues are working now to recreate the cell reprogramming in human cells. It could take years to determine if the same results can be achieved.
University of California - Los Angeles
The implications for disease treatment could be staggering. Reprogramming adult stem cells into embryonic stem cells could generate a potentially limitless source of immune-compatible cells for tissue engineering and transplantation medicine. If the work can be replicated in human cells, it may mean that a patient's skin cells, for example, could be reprogrammed to become embryonic stem cells. Those embryonic stem cells could then be prodded into becoming various cells types - beta islet cells to treat diabetes, hematopoetic cells to create a new blood supply for a leukemia patient, motor neuron cells to treat Parkinson's disease.
"If we can recreate this in human cells, it has significant implications for regenerative therapies," said Kathrin Plath, an assistant professor of biological chemistry, a researcher with the Institute for Stem Cell Biology and Medicine at UCLA (ISCBM) and co-lead author of the study. "Our reprogrammed cells were virtually indistinguishable from embryonic stem cells. We could find no evidence that they were different in any way. We were rather surprised at how well this reprogramming worked."
The finding also is significant in that this new technique could potentially replace a controversial method used to reprogram cells, somatic cell nuclear transfer (SCNT), sometimes referred to "therapeutic cloning." To date, SCNT has not been done successfully in human cells.
"If we can successfully reprogram a normal human cell into a cell with almost identical properties to those in embryonic stem cells without SCNT, it may have important therapeutic ramifications and provide us with another method to develop human stem cell lines," said Dr. Owen Witte, ISCBM director and a Howard Hughes Medical Institute investigator. "Up until now, it's been unclear whether a cell could be reprogrammed back into an embryonic stem cell state without the use of SCNT, so that makes this a very important finding."
Studies published previously had shown that the four transcription factors, which regulate expression of downstream genes and either activate or silence their expression, could reprogram cells into cells with some pluripotent properties. But they differed from embryonic stem cells in that they could not differentiate into every cell type or support development of adult tissues.
"They had very limited developmental potential," Plath said. "We took a different approach, carefully selecting from our pool of cells the reprogrammed cells that highly expressed two genes we know are essential in embryonic stem cells."
Selecting cells that highly expressed the genes, Oct4 and Nanog, essential to giving embryonic stem cells their unique characteristics resulted in reprogrammed cells with much more powerful pluripotency, Plath said.
The reprogrammed cells were not just functionally identical to embryonic stem cells. They also had identical biological structure. In a cell nucleus, DNA - an organism's unique map or instructions - wraps around histones, which serve as a kind of scaffolding for compaction of the long DNA molecule. Histones don't merely package DNA. Chemical tags on histones determine which genes are expressed or shut off in the DNA. In the reprogrammed cells, the location of the chemical tags along the DNA chromosomes were identical to those found in embryonic stem cells and, just as importantly, dramatically different from those in the fibroblasts before reprogramming. The structure of the reprogrammed cells - down to the very small chemical tags that dictate gene expression - is highly similar to that of embryonic stem cells.
Plath and her colleagues are working now to recreate the cell reprogramming in human cells. It could take years to determine if the same results can be achieved.
University of California - Los Angeles
Embryonic Stem Cells Current Events and Embryonic Stem Cells News RSSOf mice and men: Stem cells and ethical uncertainties
The recent creation of live mice from induced pluripotent stem cells (iPSCs) not only represents a remarkable scientific achievement, but also raises important issues, according to bioethicists at The Johns Hopkins University's Berman Institute of Bioethics.
NIH-funded researchers transform embryonic stem cells into human germ cells
Researchers funded in part by the National Institutes of Health have discovered how to transform human embryonic stem cells into germ cells, the embryonic cells that ultimately give rise to sperm and eggs.
Placental precursor stem cells require testosterone-free environment to survive
Trophoblast stem cells (TSCs), cells found in the layer of peripheral embryonic stem cells from which the placenta is formed, are thought to exhibit "immune privilege" that aids cell survivability and is potentially beneficial for cell and gene therapies.
Endocrine Society calls for expanded scope and funding for stem cell research
Stem cell research holds great promise for the treatment of millions of Americans with debilitating and possibly fatal diseases.
Small mechanical forces have big impact on embryonic stem cells
Applying a small mechanical force to embryonic stem cells could be a new way of coaxing them into a specific direction of differentiation, researchers at the University of Illinois report. Applications for force-directed cell differentiation include therapeutic cloning and regenerative medicine.
Fate Therapeutics announces creation of small molecule platform for commercial-scale reprogramming
Fate Therapeutics, Inc. announced today the generation of human induced-pluripotent stem cells (iPSCs) using a combination of small molecules that significantly improves the speed and efficiency of reprogramming.
A major step in making better stem cells from adult tissue
October 15, 2009 A team led by scientists from The Scripps Research Institute has developed a method that dramatically improves the efficiency of creating stem cells from human adult tissue, without the use of embryonic cells.
New strategy for mending broken hearts?
By mimicking the way embryonic stem cells develop into heart muscle in a lab, Duke University bioengineers believe they have taken an important first step toward growing a living "heart patch" to repair heart tissue damaged by disease.
Liver cells grown from patients' skin cells
Scientists at The Medical College of Wisconsin in Milwaukee have successfully produced liver cells from patients' skin cells opening the possibility of treating a wide range of diseases that affect liver function.
Major improvements made in engineering heart repair patches from stem cells
University of Washington (UW) researchers have succeeded in engineering human tissue patches free of some problems that have stymied stem-cell repair for damaged hearts.
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