The discovery that mature, adult cells can be reprogrammed back to an embryonic-like state has won this year’s Nobel Prize in Physiology or Medicine. It was awarded to two pioneers of stem-cell research, John Gurdon and Shinya Yamanaka.
Reprogrammed cells are able to regain pluripotency, the potential to differentiate into many mature cell types. Researchers hope that these cells will eventually be used in regenerative medicine, providing replacement tissue for damaged or diseased organs.
Gurdon is based at the Gurdon Institute in Cambridge, UK, and was the first person to demonstrate that cells could be reprogrammed 50 years ago. At that time, researchers thought that cellular specialization was a one-way process and that it couldn’t be reversed. Gurdon was able to prove the opposite, by removing the nucleus from a frog egg cell and replacing it with the nucleus from a tadpole’s intestinal cell. This process was also able to turn back the clock of the substitute nucleus. Even though it had already committed itself to specialization, inside the egg cell, it was able to act like an egg’s nucleus and direct the development of a normal tadpole.
Mammalian cells didn’t prove as amenable to this process as frog cells. This technique is known as cloning by nuclear transfer and it took nearly 35 years before the first cloned animal, Dolly the sheep, was born in 1996.
Shinya Yamanaka of Kyoto University, Japan, used cultured mouse cells to identify the genes that kept embryonic cells immature. Then, he tested whether any of these genes could reprogram mature cells to make them pluripotent.
In the mid-2000s, Yamanaka was close to this feat. A few months after the 2006 meeting of the International Society for Stem Cell Research in Toronto, Canada, Yamanaka announced his surprisingly simple recipe to complete his task. The activation of only four genes was enough to turn adult fibroblast cells back into pluripotent stem cells. Such induced pluripotency would allow the cells to be coaxed into different types of mature cells, including nerve and heart cells.
Both scientists state that translating these discoveries into regenerative therapies will take time, which is why it’s important for people to support it.
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1 Comment
Hats off to stem-cell researchers John Gurdon and Shinya Yamanaka for their work of reprogramming cells to become pluripotent which makes the biology omnipotent. Certainly this is a breakthrough in finding spare organs for tomorrow`s world. Cloning is already made possible by our scientists in creating Dolly Sheep and calf etc. Fortunately cloning of humans are formidden. For an artificial organ development, a full baby should be developed by cloning method and its organs harvested to help. Even if it is a very early stage, it is nothing but pure infanticide. In cloning the implanted ordinary cell in the embryo (non-nucleated), the process goes till it becomes omnipotent, then divide to become pluripotent and then multipotent to crate a full baby. In Nobel Laurettes experiment, suitable cells (ordinary) is impregnated in non-nucleated embryo allowed to reprogramme upto desired pluripotent cells, which can become ,say nerve, cell, kidney cells, heart cells, liver cells etc. These pluripotent cells are pipetted out and cultured in a suitable media for the tissue concerned to form the specialised cells which when injected into the organ like liver etc, would regenerate healthy liver cells among the diseases ones. No infanticide is observed anywhere. We expect more research and success in this method. Thank YOu.