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TAR-DNA binding protein 43 in Pick disease
Stefanie H Freeman1, Tara Spires-Jones, Bradley T Hyman
1Department of Pathology, MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02129, USA. sfreeman1@partners.org
Pick disease (PiD), a form of frontotemporal dementia, involves tau and ubiquitin Pick bodies. Some PiD cases also show TAR-DNA binding protein 43 (TDP-43) inclusions, suggesting TDP-43
Area of Science:
- Neuropathology
- Neurodegenerative Diseases
- Frontotemporal Dementia
Background:
- Pick disease (PiD) is a frontotemporal dementia defined by specific neuropathological hallmarks.
- These include frontal and temporal atrophy, neuronal loss, gliosis, and characteristic Pick bodies.
- TAR-DNA binding protein 43 (TDP-43) is implicated in other neurodegenerative conditions like frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Purpose of the Study:
- To investigate the presence and significance of TDP-43 in Pick disease.
- To determine if TDP-43 pathology is a common feature across all PiD cases.
Main Methods:
- Immunohistochemical analysis was performed on fifteen cases of Pick disease.
- Tissues were examined for the presence of tau, ubiquitin, and TDP-43.
Main Results:
- Five out of fifteen PiD cases exhibited intracytoplasmic inclusions positive for ubiquitin, tau, and TDP-43, alongside Pick bodies.
- These TDP-43 positive inclusions were smaller than the typical Pick bodies.
Conclusions:
- The presence of TDP-43 inclusions in a subset of PiD cases suggests its potential role in the disease.
- TDP-43 accumulation may be a shared mechanism in various neurodegenerative diseases.
- The variability in TDP-43 presence indicates potential distinct pathological pathways within Pick disease.
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