FIRST HUMAN-PIG EMBRYO GROWN IN LABORATORY.
For the first time, biologists have succeeded in growing human stem cells in pig embryos, shifting from science fiction to the realm of the possible the idea of developing human organs in animals for later transplant. The approach involves generating stem cells from a patient's skin, growing the desired new organ in a large animal like a pig, and then harvesting it for transplant into the patient's body. Since the organ would be made of a patient's own cells, there would be little risk of immune rejection. The human-organ growing pigs would be examples of chimeras, animals composed of two different genomes. They would be generated by implanting human stem cells into an early pig embryo, resulting in an animal composed of mixed pig and human cells. A team of biologists, led by Jun Wu and Juan Carlos Izpisua Belmonte at the Salk Institute, US, has shown that human stem cells can contribute to forming the tissues of a pig, despite the ninety million years of evolution between the two species. Another group, headed by Tomoyuki Yamaguchi and Hideyuki Sato of the University of Tokyo, and Hiromitsu Nakauchi of Stanford, has reversed diabetes in mice by inserting pancreas glands composed of mouse cells that were grown in a rat.
The Salk team's report was published in journal 'Cell', and the Stanford-Tokyo team's in journal 'Nature'. The two reports together establish the feasibility of trying to grow replacement human organs in animals, though such a goal is still far off. Many technical and ethical barriers have yet to be overcome, but the research is advancing alongside the acute need for organs. Creating chimeras, especially those with human cells, may prove controversial, given the possibility that test animals could be humanised in undesirable ways. Both Izpisua Belmonte and Nakauchi said there was a long way top go before human organs could successfully be grown in animals like pigs. Chimeras will be more immediately useful in studying human embryogenesis, testing drugs and following the progress of disease.
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