Scientists create “interspecies” animal using embryonic stem cells

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Liverpool, UK - Embrionic stem (ES) cells from a wood mouse into the early embryo of a house mouse, an international team of scientists has produced normal healthy animals made up a mixture of cells from each the two distantly related species. This is the first time that stem cells from one mammalian species have been shown to contribute extensively to development when introduced into the embryo of another, very different species.
Liverpool, UK - Embrionic stem (ES) cells from a wood mouse into the early embryo of a house mouse, an international team of scientists has produced normal healthy animals made up a mixture of cells from each the two distantly related species. This is the first time that stem cells from one mammalian species have been shown to contribute extensively to development when introduced into the embryo of another, very different species.

In an advanced online posting on Oct. 3, 2007, in the journal Human Molecular Genetics, scientists from the University of Chicago, Sun Yat-sen University, China, and the University of Liverpool, U.K., describe how they produced a viable “chimera” — a single organism with traits from two different species.

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Although both are rodents, the wood mouse (Apodemus sylvaticus) and the house mouse (Mus musculus) have evolved separately for up to 20 million years. Their genes differ by as much as 18 percent, about 10 times the difference between human and chimpanzee.

Before now, scientists have used ES cells to make chimeras within the same species or with closely related species. “There are surprisingly high degrees of conservation in developmental programs between at least some distantly related mammalian species,” said study co-author Bruce Lahn, a Howard Hughes investigator and professor of human genetics at Chicago. “When early embryonic cells from two divergent species are mixed together, they can communicate with each other properly and develop into one seamless, functional organism.”

“These results demonstrate the feasibility of differentiating ES cells into a wide range of cell types in vivo by introducing them into an evolutionary divergent host,” the authors wrote. “This interspecies approach may be the only way to study ES cells of some species, such as human ES cells, in an in vivo context.”

The scientists extracted wood mouse ES cells and introduced a gene that produced a fluorescent protein, which enabled them to visually track the descendents of the stem cells in the chimeric organisms. They then injected 15 wood mouse ES cells into each of the 1,250 house mouse blastocysts and transferred the viable embryos into 44 surrogate house mouse mothers.

From these, 220 pups were born, 16 of them (7.3 percent) showed chimerism based on their appearance. In those 16 chimeras, up to 40 percent of the cells were wood mouse cells. These cells were integrated into all of the tissues at various levels.

The chimeras appeared healthy and had no apparent defects. They did demonstrate some behavioral differences. They were less “jumpy” than a typical wood mouse but more so than a typical, much tamer, house mouse.

Although genetically different (the wood mouse has 48 chromosomes, the house mouse, 40), both of these species have similar developmental schedules. The gestation period for a wood mouse is 28 days; the gestation time for a house mouse is 21 days. They also have approximately the same body size.

The chimeras varied in terms of how much and where the injected ES cells generated tissue. “It’s completely random where the cells will develop and grow tissue,” Lahn said, adding that more studies are planned.

“We’re going to continue with these animals for a while to see if we can understand the developmental cues and learn how to manipulate the system,” Lahn said. “For example, could injected wood mouse embryonic stem cells contribute more extensively to the liver in a house mouse that carries a genetic defect that prevents it from growing its own liver? Or, could we alter the stem cells in ways that could prevent them from contributing brain tissue?”

The researchers also plan to merge mouse and rat, which have vastly different gestation periods and body sizes, as well as 20 percent genetic difference.

Key Scientific and Technological Projects of Guangdong Province and of Guangzhou, and the National Natural Science Foundation of China funded this project.

Other authors of the paper are:

Jaehyun Lee, Donghyun Park, Eric Vallender, Tammy Vallender and Li Zhang, of the University of Chicago; Shu-Nong Li, Wei-Qiang Li, Bao-Feng Ma, Tao Wang, Xin-Bing Yu and Xiu-Ming Zhang, of Sun Yat-sen University in Gaungzhou, China; Lahn, Frank Fuxiang Mao and Andy Peng Xiang, affiliated with both institutions; and John Waters of the University of Liverpool, U.K.