Federal officials are proposing to end a moratorium on funding for research that involves transplanting human stem cells
into animal embryos, a controversial practice that produces organisms know as «chimeras.»
Not exact matches
As soon as the nervous system forming in the
embryo begins to function as a whole — and not before — the cell colony begins to turn
into a genuinely individual
animal.
Among the bill's most controversial sections is legal clarification allowing research on so - called hybrid
embryos, where a human nucleus is inserted
into an
animal egg.
Under a 2015 moratorium, the National Institutes of Health does not fund research that transplants human stem cells
into early
embryos of other
animals.
When researchers create «chimeric» mice by injecting iPS cells
into early - stage mouse
embryos, the resulting
animals are unusually prone to cancer.
By using engineered zinc - finger nucleases (ZFNs) designed to target an integrated reporter and two endogenous rat genes, Immunoglobulin M (IgM) and Rab38, we demonstrate that a single injection of DNA or messenger RNA encoding ZFNs
into the one - cell rat
embryo leads to a high frequency of
animals carrying 25 to 100 % disruption at the target locus.
► The U.S. National Institutes of Health (NIH) has put funding on hold for experiments that involve «mixing human stem cells
into very early
animal embryos and letting them develop» while it «reconsiders its rules» for this type of research, Gretchen Vogel reported Wednesday.
The latter type of research, in which human cells or tissue are integrated
into animals, was given the green light in the United Kingdom in October 2008, when the British House of Commons approved a bill that expanded the country's rules governing work with human
embryos.
The patent gives California - based Geron Corp. exclusive rights to
animal embryos prepared by transferring the nucleus of a quiescent diploid donor cell
into a suitable recipient cell up to and including the blastocyst stage.
Totipotent cells are the most versatile of all stem cells; a single one can develop
into an
embryo with a placenta, and hence give rise to a fully formed
animal — in other words, a clone.
Researchers were able to complete the first genome - wide screen of a mouse by injecting small hairpin RNAs
into the
embryos of 100 pregnant mice and analyzing the
animals after birth to look for genes that contributed to tumor growth.
The application is on hold, the agency has told him, as NIH reconsiders its rules for the kind of experiments he wants to do: mixing human stem cells
into very early
animal embryos and letting them develop, a strategy that could produce tissues or organs for transplantation.
They do not, however, prohibit injecting human pluripotent cells
into the
embryos of other
animals and letting the chimeras develop.
Some worry that such human cells, when combined with
animal embryos, could develop
into brain cells, sperm, or egg cells in the chimeric offspring.
When Hayashi injected a mutant gene for PAK
into mouse
embryos and later killed the adult mice and dissected and examined their brains, she discovered that the
animals» dendritic spines — branched stalks that receive input from neighboring neurons — were short, fat, and sparse.
Transplanting a head organizer from one
embryo into another
embryo, for instance, created two complete
animals, attached to each other like Siamese twins.
But scientists have not managed to isolate such cells from farm
animals, and must rely instead on injecting genes randomly
into early
embryos.
More importantly, biotechnologists will for the first time be able to manipulate the genes of cells from farm
animals directly before growing them
into embryos.
Since 2009 NIH guidelines have prohibited funding experiments in which human stem cells are injected
into primate
embryos or in which human -
animal chimeras breed.
That and other concerns led the National Institutes of Health to announce in 2015 that it would not fund experiments that put human pluripotent stem cells, those with the ability to morph
into almost any kind of tissue or organ,
into the early
embryos of other
animals.
«Conventional techniques of producing transgenic
animals, such as microinjection of genes
into eggs and the retroviral transduction of genes
into embryos, often produce many
animals that are mosaic, which means they do not contain the foreign gene in all their cells.
In
animal systems, pluripotency can be verified through direct means: pluripotent stem cells can be introduced
into an developing
embryo and thus the cellular developmental potential of any given in vitro preparation can be directly determined by observing the amount of chimaerism or viability of organisms partially or fully derived from in vitro stem cells.
In this study, the team delved deep
into the nucleus of cells belonging to mouse and zebrafish
embryos — two important
animal models of embryonic development — in order to determine how the Dll4 gene is turned on.
The legislation would allow scientists to create
embryos for purposes of harvesting the stem cells by transferring human DNA
into animal eggs that have had most of their genetic information removed.
The team at the Central Institute for Experimental
Animals in Kawasaki, Japan, added a fluorescent gene to the marmoset
embryos, which were then transferred
into surrogate females who produced five live births.
The
embryo is then implanted
into surrogate
animal.