Page URL:

Stem cell genes altered inside living organism for first time

10 June 2019
Appeared in BioNews 1001

Genes have been edited directly in the stem cells of a living organism, a new study has found. Scientists were able to modify genes in specific stem cells in adult mice using a virus.

The research could have significance in humans in future – being able to edit genes within a living patient would be a breakthrough for genetic disease therapies.

'If you want to change a genome to correct a disease-causing gene mutation, you have to change it in the relevant stem cells,' said lead scientist Professor Amy Wagers at Harvard University in Cambridge, Massachusetts. 'If you don't change the stem cells, whatever cells you do fix may eventually be replaced with diseased cells fairly quickly. If you do fix the stem cells, they will create healthy cells that can eventually replace the diseased cells.'

At the moment, gene therapy in humans involves taking the stem cells out of the body to edit their genes, then putting them back in. The process of removing and reintroducing these cells adds a risk of complications, which would be avoided if it were possible to target stem cells in a living patient directly. 

'When you take stem cells out of the body, you take them out of the very complex environment that nourishes and sustains them, and they kind of go into shock,' said Professor Wagers. 'Isolating cells changes them. Transplanting cells changes them. Making genetic changes without having to do that would preserve the regulatory interactions of the cells – that's what we wanted to do.'

To achieve this, the researchers took advantage of different adeno-associated viruses, which can specifically target certain tissue types but do not cause disease. They engineered these viruses to deliver gene editing molecular machinery to mouse specific skin, blood and muscle stem cells or progenitor cells (a slightly more developed form of stem cell). These viruses were delivered into a specific strain of mice in which, if the cargo was successfully delivered to the target cells, a fluorescent 'reporter' gene in the cells would be activated and these cells would glow red.

The researchers saw that the reporter gene was turned on in up to 60 percent of the stem cells of skeletal muscle. In skin progenitor cells and blood stem cells, up to 27 percent and 38 percent of cells glowed red, respectively. 

'Our study demonstrates that we can permanently modify the genome of stem cells, and therefore their progenies, in their normal anatomical niche,' said Dr Mohammadsharif Tabebordbar, study co-author at the Broad Institute, also in Cambridge. 'There is a lot of potential to take this approach forward and develop more durable therapies for different forms of genetic diseases. That includes different forms of muscular dystrophy, where tissue regeneration is such an important factor.'

The work was published in the journal Cell Reports.

Editing genes at the source
The Harvard Gazette |  4 June 2019
Harvard breakthrough shows stem cells can be genetically edited in the body
New Atlas |  5 June 2019
In Situ Modification of Tissue Stem and Progenitor Cell Genomes
Cell Reports |  23 April 2019
Stem cell genes altered inside living organism for first time
Sciencealert |  6 June 2019
16 September 2019 - by Dr Yvonne Collins 
Scientists have developed a new device that uses iPSCs to create the most advanced artificial model of early human embryo development...
5 August 2019 - by Dr Yvonne Collins 
The Japanese Government has approved the first human-animal embryo experiments which could eventually lead to a new source of organs for transplant...
8 July 2019 - by Dr Elizabeth Oliver 
Scientists have used embryonic stem cells to create three-dimensional early-stage human embryos that are more complex than any previous lab-generated embryo model...
25 February 2019 - by James Close 
A new gene therapy is being developed to treat the rare genetic condition Angelman syndrome in while the affected foetus is still in the womb...
15 October 2018 - by Dr Maria Botcharova 
Researchers have bred mouse pups with genetic material from two male, or two female parents...
25 June 2018 - by Dr Melanie Krause 
For the first time, scientists from Stanford University, California, have combined CRISPR genome editing with a stem cell system to model how a genetic mutation might affect heart disease risk...
to add a Comment.

By posting a comment you agree to abide by the BioNews terms and conditions

Syndicate this story - click here to enquire about using this story.