Literature DB >> 33106888

PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study.

Kathrin Gonsior1,2, Gabriele Anna Kaucher1,2, Patrik Pelz1,2, Dorothea Schumann1,2, Melanie Gansel1,2, Sandra Kuhs3,4, Thomas Klockgether3,4, Sylvie Forlani5, Alexandra Durr5, Stefan Hauser6,7, Tim W Rattay6,7, Matthis Synofzik6,7, Holger Hengel6,7, Ludger Schöls6,7, Olaf H Rieß1,2,8, Jeannette Hübener-Schmid9,10.   

Abstract

In view of upcoming clinical trials, quantitative molecular markers accessible in peripheral blood are of critical importance as prognostic or pharmacodynamic markers in genetic neurodegenerative diseases such as Spinocerebellar Ataxia Type 3 (SCA3), in particular for signaling target engagement. In this pilot study, we focused on the quantification of ataxin-3, the protein altered in SCA3, in human peripheral blood mononuclear cells (PBMCs) acquired from preataxic and ataxic SCA3 mutation carriers as well as healthy controls, as a molecular marker directly related to SCA3 pathophysiology. We established two different highly sensitive TR-FRET-based immunoassays to measure the protein levels of either total full-length, non-expanded and expanded, ataxin-3 or specifically polyQ-expanded ataxin-3. In PBMCs, a clear discrimination between SCA3 mutation carrier and controls were seen measuring polyQ-expanded ataxin-3 protein level. Additionally, polyQ-expanded ataxin-3 protein levels correlated with disease progression and clinical severity as assessed by the Scale for the Assessment and Rating of Ataxia. Total full-length ataxin-3 protein levels were directly influenced by the expression levels of the polyQ-expanded ataxin-3 protein, but were not correlated with clinical parameters. Assessment of ataxin-3 levels in fibroblasts or induced pluripotent stem cells allowed to distinguish mutation carriers from controls, thus providing proof-of-principle validation of our PBMC findings across cell lines. Total full-length or polyQ-expanded ataxin-3 protein was not detectable by TR-FRET assays in other biofluids like plasma or cerebrospinal fluid, indicating the need for ultra-sensitive assays for these biofluids. Standardization studies revealed that tube systems, blood sampling, and PBMC preparation may influence ataxin-3 protein levels indicating a high demand for standardized protocols in biomarker studies. In conclusion, the polyQ-expanded ataxin-3 protein is a promising candidate as a molecular target engagement marker in SCA3 in future clinical trials, determinable even in-easily accessible-peripheral blood biomaterials. These results, however, require validation in a larger cohort and further standardization of modifying conditions.

Entities:  

Keywords:  Ataxin-3; Biomarker; Peripheral blood mononuclear cell (PBMC); Spinocerebellar ataxia type 3 (SCA3)/Machado–Joseph disease (MJD); Time-resolved fluorescence energy transfer (TR-FRET)

Year:  2020        PMID: 33106888      PMCID: PMC7990753          DOI: 10.1007/s00415-020-10274-y

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  38 in total

1.  A more efficient method to generate integration-free human iPS cells.

Authors:  Keisuke Okita; Yasuko Matsumura; Yoshiko Sato; Aki Okada; Asuka Morizane; Satoshi Okamoto; Hyenjong Hong; Masato Nakagawa; Koji Tanabe; Ken-ichi Tezuka; Toshiyuki Shibata; Takahiro Kunisada; Masayo Takahashi; Jun Takahashi; Hiroh Saji; Shinya Yamanaka
Journal:  Nat Methods       Date:  2011-04-03       Impact factor: 28.547

2.  MicroRNA pathways modulate polyglutamine-induced neurodegeneration.

Authors:  Julide Bilen; Nan Liu; Barrington G Burnett; Randall N Pittman; Nancy M Bonini
Journal:  Mol Cell       Date:  2006-10-06       Impact factor: 17.970

3.  Neurologic findings in Machado-Joseph disease: relation with disease duration, subtypes, and (CAG)n.

Authors:  L B Jardim; M L Pereira; I Silveira; A Ferro; J Sequeiros; R Giugliani
Journal:  Arch Neurol       Date:  2001-06

4.  A combinatorial approach to identify calpain cleavage sites in the Machado-Joseph disease protein ataxin-3.

Authors:  Jonasz J Weber; Matthias Golla; Giambattista Guaitoli; Pimthanya Wanichawan; Stefanie N Hayer; Stefan Hauser; Ann-Christin Krahl; Maike Nagel; Sebastian Samer; Eleonora Aronica; Cathrine R Carlson; Ludger Schöls; Olaf Riess; Christian J Gloeckner; Huu P Nguyen; Jeannette Hübener-Schmid
Journal:  Brain       Date:  2017-05-01       Impact factor: 13.501

5.  Scale for the assessment and rating of ataxia: development of a new clinical scale.

Authors:  T Schmitz-Hübsch; S Tezenas du Montcel; L Baliko; J Berciano; S Boesch; C Depondt; P Giunti; C Globas; J Infante; J-S Kang; B Kremer; C Mariotti; B Melegh; M Pandolfo; M Rakowicz; P Ribai; R Rola; L Schöls; S Szymanski; B P van de Warrenburg; A Dürr; T Klockgether; Roberto Fancellu
Journal:  Neurology       Date:  2006-06-13       Impact factor: 9.910

6.  Intrafamilial variability in Machado-Joseph disease.

Authors:  S H Subramony; R D Currier
Journal:  Mov Disord       Date:  1996-11       Impact factor: 10.338

Review 7.  Pathways to motor incoordination: the inherited ataxias.

Authors:  Franco Taroni; Stefano DiDonato
Journal:  Nat Rev Neurosci       Date:  2004-08       Impact factor: 34.870

8.  Diagnostic and prognostic values of PBMC proteins in amyotrophic lateral sclerosis.

Authors:  Silvia Luotti; Laura Pasetto; Luca Porcu; Valter Torri; Saioa R Elezgarai; Serena Pantalone; Melania Filareti; Massimo Corbo; Christian Lunetta; Gabriele Mora; Valentina Bonetto
Journal:  Neurobiol Dis       Date:  2020-02-20       Impact factor: 5.996

9.  Generation of an induced pluripotent stem cell line from a patient with spinocerebellar ataxia type 3 (SCA3): HIHCNi002-A.

Authors:  Stefanie Nicole Hayer; Yvonne Schelling; Jeannette Huebener-Schmid; Jonasz Jeremiasz Weber; Stefan Hauser; Ludger Schöls
Journal:  Stem Cell Res       Date:  2018-06-11       Impact factor: 2.020

10.  Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression.

Authors:  Andreas Weiss; Ulrike Träger; Edward J Wild; Stephan Grueninger; Ruth Farmer; Christian Landles; Rachael I Scahill; Nayana Lahiri; Salman Haider; Douglas Macdonald; Chris Frost; Gillian P Bates; Graeme Bilbe; Rainer Kuhn; Ralph Andre; Sarah J Tabrizi
Journal:  J Clin Invest       Date:  2012-09-17       Impact factor: 14.808

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  2 in total

Review 1.  Rating scales and biomarkers for CAG-repeat spinocerebellar ataxias: Implications for therapy development.

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