Tau protein quantification in skin biopsies differentiates tauopathies from alpha-synucleinopathies

Author:

Vacchi Elena12ORCID,Lazzarini Edoardo3,Pinton Sandra1,Chiaro Giacomo14,Disanto Giulio4,Marchi Francesco5,Robert Thomas25,Staedler Claudio4,Galati Salvatore24,Gobbi Claudio24,Barile Lucio236,Kaelin-Lang Alain1247,Melli Giorgia124

Affiliation:

1. Laboratories for Translational Research, Neurocenter of Southern Switzerland, Ente Ospedaliero Cantonale , Lugano , Switzerland

2. Faculty of Biomedical Sciences, Università della Svizzera italiana , Lugano , Switzerland

3. Laboratory for Cardiovascular Theranostics, Cardiocentro Ticino Institute, Ente Ospedaliero Cantonale , Lugano , Switzerland

4. Neurology Department, Neurocenter of Southern Switzerland, Ente Ospedaliero Cantonale , Lugano , Switzerland

5. Neurosurgery Department, Neurocenter of Southern Switzerland, Ente Ospedaliero Cantonale , Lugano , Switzerland

6. Institute of Life Science, Scuola Superiore Sant’Anna , Pisa , Italy

7. Department of Neurology, Inselspital, Bern University Hospital, University of Bern , Bern , Switzerland

Abstract

Abstract Abnormal accumulation of microtubule-associated protein tau (τ) is a characteristic feature of atypical parkinsonisms with tauopathies, such as progressive supranuclear palsy and corticobasal degeneration. However, pathological τ has also been observed in α-synucleinopathies like Parkinson’s disease and multiple system atrophy. Based on the involvement of the peripheral nervous system in several neurodegenerative diseases, we characterized and compared τ expression in skin biopsies of patients clinically diagnosed with Parkinson’s disease, multiple system atrophy, progressive supranuclear palsy and corticobasal degeneration and in healthy control subjects. In all groups, τ protein was detected along both somatosensory and autonomic nerve fibres in the epidermis and dermis by immunofluorescence. We found by western blot the presence of mainly two different bands at 55 and 70 kDa, co-migrating with 0N4R/1N3R and 2N4R isoforms, respectively. At the RNA level, the main transcript variants were 2N and 4R, and both were more expressed in progressive supranuclear palsy/corticobasal degeneration by real-time PCR. Enzyme-linked immunosorbent assay demonstrated significantly higher levels of total τ protein in skin lysates of progressive supranuclear palsy/corticobasal degeneration compared to the other groups. Multivariate regression analysis and receiver operating characteristics curve analysis of τ amount at both sites showed a clinical association with tauopathies diagnosis and high diagnostic value for progressive supranuclear palsy/corticobasal degeneration versus Parkinson’s disease (sensitivity 90%, specificity 69%) and progressive supranuclear palsy/corticobasal degeneration versus multiple system atrophy (sensitivity 90%, specificity 86%). τ protein increase correlated with cognitive impairment in progressive supranuclear palsy/corticobasal degeneration. This study is a comprehensive characterization of τ in the human cutaneous peripheral nervous system in physiological and pathological conditions. The differential expression of τ, both at transcript and protein levels, suggests that skin biopsy, an easily accessible and minimally invasive exam, can help in discriminating among different neurodegenerative diseases.

Funder

FIDINAM

Parkinson Schweiz

Jacques und Gloria Gossweiler Stiftung

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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