"Reprogramming somatic cells into pluripotent embryonic stem cells (ESCs) by somatic cell nuclear transfer (SCNT) has been envisioned as an approach for generating patient-matched nuclear transfer (NT)-ESCs for studies of disease mechanisms and for developing specific therapies. Past attempts to produce human NT-ESCs have failed secondary to early embryonic arrest of SCNT embryos. Here, we identified premature exit from meiosis in human oocytes and suboptimal activation as key factors that are responsible for these outcomes. Optimized SCNT approaches designed to circumvent these limitations allowed derivation of human NT-ESCs. When applied to premium quality human oocytes, NT-ESC lines were derived from as few as two oocytes. NT-ESCs displayed normal diploid karyotypes and inherited their nuclear genome exclusively from parental somatic cells. Gene expression and differentiation profiles in human NT-ESCs were similar to embryo-derived ESCs, suggesting efficient reprogramming of somatic cells to a pluripotent state."The Verge:
An international team of scientists announced today that for the first time ever, they were able to create new human stem cells by cloning older, fully mature human cells.
The process cannot be used to create full human clones, as the scientists involved were quick to point out, but it does allow for cells to be grown to fit specific functions within an individual's body — resulting in new, patient-specific liver cells or heart cells that actually pulse on their own, for example.
Eventually, scientists hope to refine the process to the point it could be used to help treat disease and even create whole custom organs, but that is likely to be several years away at the earliest. "While there is much work to be done in developing safe and effective stem cell treatments, we believe this is a significant step forward in developing the cells that could be used in regenerative medicine," said Shoukhrat Mitalipov, the leader of the research team and a senior scientist at the Oregon National Primate Research Center (ONPRC), in a news release.
The research team was led by scientists at the Oregon Health & Science University, who used a technique similar to the one that created Dolly the sheep, the first mammal cloned from adult cells, back in 1996. In a basic sense, this method involves taking an adult cell from a patient's body, sucking out the central portion containing DNA (the nucleus), then injecting this material into an empty egg cell donated by another human volunteer. The genetic material from the adult cell tells the empty egg cell what type it should mature into.
Many other scientific teams tried and failed to use this process to clone human cells over the years, and although other groups did manage to get it working in monkeys, the new research results are the first successful time the process has been successful for human cells. The team was able to overcome previous failures by using a chemical reaction to slow down one phase of a human cell's natural process of dividing into more copies of itself. They reported their work in a paper published online today in the journal Cell.
Importantly, the process uses relies on human reproductive eggs donated by female volunteers, but which have not been fertilized, meaning they are not able to mature into full human babies if left on their own. The unfertilized eggs used in this study were donated by several young women recruited through a university program and paid between $3,000 and $7,000 in compensation. The researchers behind the new work say the fact the donor cells were unfertilized should help avoid the ongoing controversy over other previous research involving the destruction of fertilized embryos, which are able grow into full human beings if left up to nature. But other scientists aren't so sure, telling NPR the advance is likely to reignite the debate.