Cloned stem cells offer high fidelity

OHSU, Center for Embryonic Cell and Gene Therapy

Human embryonic stem cells made via nuclear transfer, also known as cloning.

Scientists have established two ways to take differentiated cells from one person and generate stem cells capable of forming all cell types in the body most recently by cloning. Research published today in Nature1 compares genetically identical human stem cells made by different techniques and reveals differences in gene expression that might be important for medical research and for cell therapies.

Pluripotent stem cells can produce large supplies of, say, neurons or heart muscle, so are valuable for studying diseases and, potentially, for treating them. Human pluripotent stem cells were first made2 in 1998 from embryos left over from fertility treatments, and pluripotent stem cells produced by this method are still considered the gold standard because there is no question that embryos can produce all types of tissue in the body.

The newer techniques, called nuclear transfer and genetic reprogramming, can use cells from living people to make pluripotent stem cells that are genetically matched to a patient. For research purposes, matching provides cells from people whose disease history is known. For therapies, matching means that cells are more likely to be suitable for therapies.

Last year, Shoukhrat Mitalipov, a cell biologist at the Oregon Health and Science University in Portland, and his colleagues became the first to produce human pluripotent stem cells using nuclear transfer3, a technique also known as cloning. They took the nucleus from a cultured skin cell, placed it in an unfertilized egg that had had its nucleus removed, then made embryonic stem (ES) cells from the resultant embryo.

In the paper published today, Mitalipov and his collaborators compared cloned ES cells to 'induced pluripotent' stem (iPS) cells made by inserting reprogramming genes into cells from the same batch of cultured skin cells used to make the cloned ES cells.

In neither case did the genetic material return fully to an embryonic-like state, says Mitalipov, but one technique was the clear winner. Nuclear transfer doesn't do a perfect job of resetting, but in general it does a very, very good job in relation to iPS reprogramming.

To measure the relative quality of the two types directly, they saw how they measured next to the 'golden standard' of cells from discarded embryos by looking at their patterns of methylation, a type of 'epigenetic' modification of DNA, meaning that it affects gene expression without changing the underlying gene sequences.

Methylation patterns of nuclear-transfer ES cells were closer to those from fertilized eggs than were methylation patterns in iPS cells. More than 1,200 genes were expressed differently in the three cell types; most of these differences, about 65%, were between iPS cells and the two types of ES cells. These differences, says Mitalipov, could mean that ES cells from nuclear transfer are better able than iPS cells to mature into other cell types.

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Cloned stem cells offer high fidelity