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Stem Cell Research and Application Timeline

June 2013: Pluripotent Stem Cells Derived from Cloned Human Embryos

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1990: President George H.W. Bush Vetos Bill Lifting Moratorium
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Timeline of major events in stem cell research policy

Circuit] reasoning and conclusions, must find that defendants reasonably interpreted the Dickey-Wicker Amendment to permit funding for human embryonic stem cell research because such research is not 'research in which a human embryo or embryos are destroyed' That policy question is not answered by any congressional law, and it has fallen on three presidential administrations to provide an answer.

For all three such administrations, Democratic and Republican, the answer has been to permit federal funding. They have differed only as to the path forward.

See the full text of the ruling here. Researchers at Cedars-Sinai Medical Center and Johns Hopkins University publish results from a clinical trial in which adult stem cells were extracted from patients following a heart attack. In the first demonstrated case of therapeutic regeneration, the treatment decreases scarring and leads to regrowth of heart tissue.

In a decision favorable to proponents of ES cell research, the U. Sebelius , thereby upholding the previous ruling of the D. By removing the DNA from an egg cell and replacing it with genetic material from a skin cell, scientists create stem cells that can be programmed into becoming many different cell types, including the contracting cardiomyocytes that make up our heart muscle. Nuclear transfer NT -ES cells hold great promise for regenerative medicine because the resulting stem cells are a genetic match to the skin cell donor.

An FDA-approved clinical trial finds that treatment with ES cells improves sight in over half of 18 patients suffering from macular degeneration. The study, published in The Lancet , shows that transplantation of ES cells is safe in the long-term. Don't leave advocacy to others: The guidelines stipulate that: Human embryonic stem cells must be derived with private funds from frozen embryos from fertility clinics; That they must have been created for fertility treatment purposes; That they be in excess of the donor's clinical need; and That they be obtained with consent of the donor.

President Bush prohibits federal funding of most human embryonic stem cell research President George W. Sebelius, the most noteworthy court case regarding the government's funding of embryonic stem cell research, is filed A group of plaintiffs led by adult stem cell scientists James Sherley, M.

District Court for the District of Columbia rules in favor of embryonic stem cell research in Sherley v. Martin Evans Nobel Prize, and Matt Kauffman were the first to identify, isolate and successfully culture ES cells using mouse blastocysts in []. This is possible because scientists can modify the genome of a mouse in its ES cells and then inject those modified cells into mouse blastocysts. This means that when the blastocyst develops into an adult mouse, every cell its body will have the modification of interest.

For the first time, scientists could, in theory, generate all the building blocks of our body in unlimited amounts. It was possible to have cell types for testing new therapeutics and perhaps even new transplantation methods that were previously not possible. Yet, destroying human embryos to isolate cells presented ethical and technical hurdles. How could one circumvent that procedure? Sir John Gurdon showed in the early s that, contrary to the prevalent belief back then, cells are not locked in their differentiation state and can be reverted to a more primitive state with a higher developmental potential.

He demonstrated this principle by injecting the nucleus of a differentiated frog cell into an egg cell from which the nucleus had been removed.

This is commonly known as reproductive cloning, which was used to generate Dolly the Sheep. When allowed to develop, this egg gave rise to a fertile adult frog, proving that differentiated cells retain the information required to give rise to all cell types in the body.

More than forty years later, Shinya Yamanaka and colleagues shocked the world when they were able to convert skin cells called fibroblasts into pluripotent stem cells by altering the expression of just four genes [].

This represented the birth of induced pluripotent stem cells, or iPS cells see Figure 1, right column. The enormous importance of these findings is hard to overstate, and is perhaps best illustrated by the fact that, merely six years later, Gurdon and Yamanaka shared the Nobel Prize in Physiology or Medicine []. Today, these cells are the hope of personalized medicine, as they allow one to capture the unique genome of each individual in a cell type that can be used to generate, in principle, all cell types in our body, as illustrated on the right panel of Figure 1.

The replacement of diseased tissues or organs without facing the barrier of immune rejection due to donor incompatibility thus becomes approachable in this era of iPS cells and is the object of intense research []. The first proof-of-principle study showing that iPS cells can potentially be used to correct genetic diseases was carried out in the laboratory of Rudolf Jaenisch.

In brief, tail tip cells from mice with a mutation causing sickle cell anemia were harvested and reprogrammed into iPS cells. The mutation was then corrected in these iPS cells, which were then differentiated into blood progenitor cells and transplanted back into the original mice, curing them []. Even though iPS cells have been found not to completely match ES cells in some instances, detailed studies have failed to find consistent differences between iPS and ES cells [].

This similarity, together with the constant improvements in the efficiency and robustness of generating iPS cells, provides bright prospects for the future of stem cell research and stem cell-based treatments for degenerative diseases unapproachable with more conventional methods.

Cytological demonstration of the clonal nature of spleen colonies derived from transplanted mouse marrow cells. The distribution of colony-forming cells among spleen colonies. J Cell Comp Physiol , 62 3: Establishment in culture of pluripotential stem cells from mouse embryos.

Transgenesis and Induced Mutation. Embryonic stem cell lines derived from human blastocysts. Science , Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors.

How induced pluripotent stem cells are redefining personalized medicine. Treatment of sickle cell anemia mouse model with iPS cells generated from autologous skin. Must learn new tools and technologies to make synapse and build multi-layered tissues, e.

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The information used to compile this Stem Cell Research Timeline comes from many different sources, including the National Institutes of Health. A useful list of links to other stem cell research timelines from around the Web can be found at the bottom of this page.

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Yesterday, the potential of stem cells to revolutionise medicine got a huge boost with news of an ultra-versatile kind of stem cell from adult mouse cells using a remarkably simple method. This timeline takes you through the ups and downs of .

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From early fetal tissue research to the first successful human treatments, this timeline documents the progress in stem cell science, and the policies that have impeded or promoted it. The stories of research involving human embryonic stem cells and the policy governing that work are intertwined and stretch back into the mids. History of Stem Cell Research — A Timeline Wrights/Giemsa stained human embryonic stem cell (hESC) colony on murine embryonic fibroblast feeder cells. The colony contains roughly individual hESCs.

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Timeline: A brief history of stem cell research Science Progress | June 15, From early fetal tissue research to the first successful human treatments, this timeline documents the progress in stem cell science, and the . Timeline of major events in stem cell research policy Stem cells have been used in medicine since the ’s when bone marrow transplants were first used to treat leukemia. Congressional involvement in stem cell policy started as early as