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Title: Nuclear localization of SMN and FUS is not altered in fibroblasts from patients with sporadic ALS.

Authors: Kariya, Shingo; Sampson, Jacinda B; Northrop, Lesley E; Luccarelli, Christopher M; Naini, Ali B; Re, Diane B; Hirano, Michio; Mitsumoto, Hiroshi

Published In Amyotroph Lateral Scler Frontotemporal Degener, (2014 Dec)

Abstract: Abstract Sporadic amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with no established biological marker. Recent observation of a reduced number of gems (survival motor neuron protein (SMN)-positive nuclear bodies) in cells from patients with familial ALS and the mouse models suggests an involvement of SMN in ALS pathology. At a molecular level, fused in sarcoma (FUS), one of the familial ALS-linked proteins, has been demonstrated to directly interact with SMN, while impaired nuclear localization of mutated FUS causes defective gem formation. Our objective was to determine whether gems and/or nuclear FUS levels in skin derived fibroblasts from sporadic ALS patients are consistently reduced and thus could constitute a novel and readily available biomarker of the disease. Fibroblasts from 20 patients and 17 age-matched healthy controls were cultured and co-immunostained for SMN and FUS. Results showed that no difference was detected between the two groups in the number of gems and in expression pattern of FUS. The number of gems negatively correlated with the age at biopsy in both ALS and control subjects. In conclusion, the expression pattern of SMN and FUS in fibroblasts cannot serve as a biomarker for sporadic ALS. Donor age-dependent gem reduction is a novel observation that links SMN with cellular senescence.

PubMed ID: 24809826 Exiting the NIEHS site

MeSH Terms: Aged; Amyotrophic Lateral Sclerosis/pathology*; Biopsy; Case-Control Studies; Cell Nucleus/metabolism*; Cells, Cultured; Female; Fibroblasts/pathology; Fibroblasts/ultrastructure*; Humans; Male; Middle Aged; RNA-Binding Protein FUS/genetics; RNA-Binding Protein FUS/metabolism*; Skin/pathology; Statistics as Topic; Survival of Motor Neuron 1 Protein/genetics; Survival of Motor Neuron 1 Protein/metabolism*

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