Summary: Converting skin cell samples into neurons helps researchers gain a better understanding of the mechanisms of Huntington’s disease.
Source: Lund University
Researchers at Lund University in Sweden have developed a new method for studying age-related brain disorders.
The researchers have focused on the neurodegenerative disorder Huntington’s disease and the results have now been published in the journal Brain.
Basic medical research often faces the challenge of developing disease models that correspond to specific disease mechanisms or the disease to be studied. This is a challenge that needs to be solved in order to produce new effective treatments.
One example of a disease that is difficult to model for an understanding of the underlying mechanisms is Huntington’s disease. In part, this is due to the difficulty in recreating adequate animal or cellular models.
By reprogramming skin cells into neurons, Johan Jakobsson and his research group have been able to study Huntington’s disease in an innovative way that he believes could be significant for successful studies of several age-related brain disorders.
“We took skin biopsies from patients living with Huntington’s disease and reprogrammed the skin biopsies into neurons. We then compared these neurons with reprogrammed neurons from healthy people. The results are very interesting. We have found several defects that explain some of the disease mechanisms in neurons from patients with Huntington’s disease.
By reprogramming skin cells into neurons, Johan Jakobsson and his research group have been able to study Huntington’s disease in an innovative way that he believes could be significant for successful studies of several age-related brain disorders. Image is in the public domain
“Among other things, we observed that neurons from patients with Huntington’s disease show problems in breaking down and recycling a particular kind of protein—which can lead to a lack of energy in these cells,” says Johan Jakobsson, professor of neuroscience at Lund University.
The researchers have also measured the biological age of the cells and observed that the reprogrammed neurons retain their biological age, which is significant if they are to be used for research in the new model system.
“One very important component in our new model system is the age of the neurons. It is possible to measure a cell’s ‘biological age,’ which we have done, and these cells retain their true biological age. In other words, the reprogrammed neurons are old, making the model system relevant in the study of other age-related neurodegenerative disorders such as Parkinson’s and Alzheimer’s,” says Johan Jakobsson.
Huntington’s disease is fatal, and scientists are yet to find any treatment or cure.
“We believe our model will provide answers and clues that are significantly more relevant for the disease than the clues obtained from animal studies, and that in the long term it will lead to breakthroughs for some form of treatment,” says Johan Jakobsson.
About this genetics and Huntington’s disease research news
Author: Press OfficeSource:Lund UniversityContact: Press Office – Lund University
Image: The image is in the public domain
Original Research: Open access.
“Distinct subcellular autophagy impairments in induced neurons from patients with Huntington’s disease ” by Karolina Pircs et al et al. Brain
Distinct subcellular autophagy impairments in induced neurons from patients with Huntington’s disease
Huntington’s disease is a neurodegenerative disorder caused by CAG expansions in the huntingtin (HTT) gene. Modelling Huntington’s disease is challenging, as rodent and cellular models poorly recapitulate the disease as seen in aging humans. To address this, we generated induced neurons through direct reprogramming of human skin fibroblasts, which retain age-dependent epigenetic characteristics.
Huntington’s disease induced neurons (HD-iNs) displayed profound deficits in autophagy, characterized by reduced transport of late autophagic structures from the neurites to the soma. These neurite-specific alterations in autophagy resulted in shorter, thinner and fewer neurites specifically in HD-iNs. CRISPRi-mediated silencing of HTT did not rescue this phenotype but rather resulted in additional autophagy alterations in control induced neurons, highlighting the importance of wild-type HTT in normal neuronal autophagy.
In summary, our work identifies a distinct subcellular autophagy impairment in adult patient derived Huntington’s disease neurons and provides a new rationale for future development of autophagy activation therapies.