Scientists have taken a vital step forward in understanding how cells can be reprogrammed to become stem cells.
New research could pave the way to generate these stem cells efficiently to better understand and develop treatments for diseases such as multiple sclerosis, Parkinson’s disease and muscular degeneration.
The study of how these cells - known as induced pluripotent stem cells (iPSCs) - were reprogramed was led by the University of Edinburgh and is published in the journal Nature.
Scientists found that the process by which iPSCs are created is not simply a reversal of how skin cells are generated in normal human development.
Researchers made the discovery by tracking the change of skin cells during the reprogramming process.
All cells in the human body begin life as a mass of cells, with the capacity to change into any specialised cell, such as a skin or muscle cell.
By returning adult cells to this original state and recreating the cell type needed for treatment scientists hope to find ways of tackling diseases such as MS, in which cells become faulty and need to be replaced.
Scientists have been able to create stem cells in this way since 2006 but, until now, it has not been clear how adult cells ‘forget’ their specialised roles to be reprogrammed by scientists.
Experts say that current methods of iPSCs production are time consuming and costly. It takes around four weeks to make human stem cells and even then the process does not always work.
Researchers say that their new insight will enable them to streamline the stem cell production process.
The finding may also shed light on how to create different cell types - like muscle or brain cells - that can be used to improve our understanding of diseases and treatment.
As exciting as this technology is, we still know very little about how cell reprogramming actually works. Using a new technique, we have improved our understanding of the process. Our work marks an exciting step towards ensuring that induced pluripotent stem cells technology will meet its full potential.
The study was funded by the European Research Council, the Medical Research Council, the Anne Rowling Regenerative Neurology Clinic and the Darwin Trust of Edinburgh.