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Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) belong to a spectrum of neurodegenerative diseases with overlapping symptoms, characterized by muscle wasting, paralysis, dementia, and other serious impairments. There are currently no effective treatments. Many patients have a common hallmark: A protein called TDP-43 clumps together in the neurons of the brain to form tiny lumps. Researchers at DZNE and Ulm University Hospital, together with international experts, have now discovered that these pathological changes primarily affect certain cells.
These findings, published in the scientific journal “Nature Communications”, could contribute to the development of new therapies.
For their study, the research team led by Prof. Karin Danzer examined brain tissue from deceased patients with ALS, with a mixed form of ALS and FTD, as well as from individuals who had not shown neurological symptoms during their lifetime. All samples came from the “motor cortex”, a brain area responsible for movement control. In total, neurons from around 80 individuals in Germany, the Netherlands, Scotland, and the United States were analyzed using advanced techniques.
“In ALS, as well as in the mixed form of ALS and FTD, TDP-43 deposits occur in different regions of the brain. However, the motor cortex is particularly relevant for movement disorders, which is why we focused on this area,” explains Karin Danzer, a research group leader at DZNE’s Ulm site and at Ulm University Hospital. The researchers found that not all neurons in this area are equally affected. “The protein aggregates occur predominantly within excitatory cells, that is, within neurons that serve to transmit and amplify nerve signals. These cells seem to be particularly susceptible to the disease. This phenomenon is referred to as selective vulnerability and known for a long time in the field. In addition, within the affected neurons, we found five subgroups. Each of these is impacted by the disease in a specific way,” explains Danzer.
Disease mechanisms
The findings are based on the “transcriptome” of affected neurons. This molecular fingerprint provides information about which genes are active in affected cells and therefore enable to distinguish pathological processes in different cells. Based on this signature, the researchers were also able to identify cell type-specific changes. “Our data offer insights into disease mechanisms and thus point to possible targets for therapy development. For example, one can see how the activity of certain genes is altered depending on the cell type. The observation that not all neurons are equally affected suggests that future therapies will need to be tailored to specific cell types in order to combat the disease effectively,” says Danzer.
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About Deutsches Zentrum für Neurodegenerative Erkrankungen, DZNE (German Center for Neurodegenerative Diseases): DZNE is one of the world’s leading research centers for neurodegenerative diseases such as Alzheimer’s, Parkinson’s and ALS, which are associated with dementia, movement disorders and other serious health impairments. These diseases place an enormous burden on patients and their families, but also on society and the economy of healthcare. DZNE contributes significantly to the development and translation into practice of novel strategies for prevention, diagnosis, care and treatment. DZNE comprises ten sites across Germany and collaborates with universities, university hospitals, research centers and other institutions in Germany and throughout the world. DZNE is state-funded and a member of the Helmholtz Association and of the German Centers for Health Research. https://www.dzne.de/en
Multi-modal dissection of cell-type specific TDP-43 pathology in the motor cortex, Wolfgang Ruf et al., Nature Communications (2026), DOI: 10.1038/s41467-026-69944-6
https://www.dzne.de/im-fokus/meldungen/2026/hirnerkrankungen-manche-nervenzellen... German version
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