STOCKHOLM - Scientists from Britain and Japan shared the Nobel Prize in Medicine yesterday for the discovery that adult cells can be re-programmed back into stem cells that can turn into any kind of tissue and may one day repair damaged organs.
John Gurdon, 79, of the Gurdon Institute in Cambridge, Britain, and Shinya Yamanaka, 50, of Kyoto University in Japan, discovered ways to create tissue that would act like embryonic cells, without the need to harvest embryos.
They share the R10.7-million prize equally.
"These ground-breaking discoveries have completely changed our view of the development and specialisation of cells," the Nobel Assembly at Stockholm's Karolinska Institute said in a statement.
The big hope for stem cells is that they can be used to replace damaged tissues in everything, from spinal cord injuries to Parkinson's disease.
All of the tissue in the body starts as stem cells, before developing into mature skin, blood, nerves, muscle and bone.
Scientists once thought it was impossible to turn adult tissue back into stem cells, which meant that new stem cells could only be created by harvesting embryos.
But Yamanaka and Gurdon showed that development can be reversed, turning adult cells back into cells that behave like embryos.
With "induced pluripotency stem cells", or iPS cells, ordinary skin or blood cells from adults are transformed back into stem cells which doctors hope will be able to repair damaged organs without being rejected by the immune system.
There are concerns, however, that iPS cells could grow out of control and develop into tumours.
"The eventual aim is to provide replacement cells of all kinds," Gurdon's Institute explains on its website.
"We would like to be able to find a way of obtaining spare heart or brain cells from skin or blood cells.
"The important point is that the replacement cells need to be from the same individual, to avoid problems of rejection and hence of the need for immunosuppression."
Hope that stem cells can replace damaged tissues
STOCKHOLM - Scientists from Britain and Japan shared the Nobel Prize in Medicine yesterday for the discovery that adult cells can be re-programmed back into stem cells that can turn into any kind of tissue and may one day repair damaged organs.
John Gurdon, 79, of the Gurdon Institute in Cambridge, Britain, and Shinya Yamanaka, 50, of Kyoto University in Japan, discovered ways to create tissue that would act like embryonic cells, without the need to harvest embryos.
They share the R10.7-million prize equally.
"These ground-breaking discoveries have completely changed our view of the development and specialisation of cells," the Nobel Assembly at Stockholm's Karolinska Institute said in a statement.
The big hope for stem cells is that they can be used to replace damaged tissues in everything, from spinal cord injuries to Parkinson's disease.
All of the tissue in the body starts as stem cells, before developing into mature skin, blood, nerves, muscle and bone.
Scientists once thought it was impossible to turn adult tissue back into stem cells, which meant that new stem cells could only be created by harvesting embryos.
But Yamanaka and Gurdon showed that development can be reversed, turning adult cells back into cells that behave like embryos.
With "induced pluripotency stem cells", or iPS cells, ordinary skin or blood cells from adults are transformed back into stem cells which doctors hope will be able to repair damaged organs without being rejected by the immune system.
There are concerns, however, that iPS cells could grow out of control and develop into tumours.
"The eventual aim is to provide replacement cells of all kinds," Gurdon's Institute explains on its website.
"We would like to be able to find a way of obtaining spare heart or brain cells from skin or blood cells.
"The important point is that the replacement cells need to be from the same individual, to avoid problems of rejection and hence of the need for immunosuppression."
This article was first published in the printed newspaper and eEdition on 9 October 2012. Click on this link to view the eEdition
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