Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Institute: MPI für molekulare Biomedizin     Collection: Jahrbuch 2018 (publ. 2017, arch)     Display Documents



  history
ID: 744108.0, MPI für molekulare Biomedizin / Jahrbuch 2018 (publ. 2017, arch)
Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis
Authors:Scekic-Zahirovic, J.; Oussini, H. E.; Mersmann, S.; Drenner, K.; Wagner, M.; Sun, Y.; Allmeroth, K.; Dieterle, S.; Sinniger, J.; Dirrig-Grosch, S.; Rene, F.; Dormann, D.; Haass, C.; Ludolph, A. C.; Lagier-Tourenne, C.; Storkebaum, E.; Dupuis, L.
Date of Publication (YYYY-MM-DD):2017-06
Title of Journal:Acta Neuropathol
Volume:133
Issue / Number:6
Start Page:887
End Page:906
Review Status:Internal review
Audience:Not Specified
Abstract / Description:Motor neuron-extrinsic mechanisms have been shown to participate in the pathogenesis of ALS-SOD1, one familial form of amyotrophic lateral sclerosis (ALS). It remains unclear whether such mechanisms contribute to other familial forms, such as TDP-43 and FUS-associated ALS. Here, we characterize a single-copy mouse model of ALS-FUS that conditionally expresses a disease-relevant truncating FUS mutant from the endogenous murine Fus gene. We show that these mice, but not mice heterozygous for a Fus null allele, develop similar pathology as ALS-FUS patients and a mild motor neuron phenotype. Most importantly, CRE-mediated rescue of the Fus mutation within motor neurons prevented degeneration of motor neuron cell bodies, but only delayed appearance of motor symptoms. Indeed, we observed downregulation of multiple myelin-related genes, and increased numbers of oligodendrocytes in the spinal cord supporting their contribution to behavioral deficits. In all, we show that mutant FUS triggers toxic events in both motor neurons and neighboring cells to elicit motor neuron disease.
Free Keywords:Amyotrophic Lateral Sclerosis/*metabolism/pathology; Animals; Axons/metabolism/pathology; Cytoplasm/metabolism/pathology; Disease Models, Animal; Male; Mice, Inbred C57BL; Mice, Transgenic; Motor Activity/physiology; Motor Neurons/*metabolism/pathology; Muscle, Skeletal/innervation/metabolism/pathology; Mutation; Nerve Degeneration/metabolism/pathology; Oligodendroglia/metabolism/pathology; RNA, Messenger/metabolism; RNA-Binding Protein FUS/genetics/*metabolism; Spinal Cord/metabolism/pathology; *Amyotrophic lateral sclerosis; *Fronto-temporal dementia; *Mouse models; *Non-cell autonomous mechanisms; *RNA-binding proteins
External Publication Status:published
Document Type:Article
Communicated by:MPI für molekulare Biomedizin
Affiliations:MPI für molekulare Biomedizin
External Affiliations:Faculte de Medecine, UMR-S1118, Universite de Strasbourg, 67085, Strasbourg, France. Molecular Neurogenetics Laboratory, Max Planck Institute for Molecular Biomedicine, Muenster, Germany. Faculty of Medicine, University of Muenster, Muenster, Germany. Department of Neurosciences, Ludwig Institute for Cancer Research, University of California, San Diego, USA. BioMedical Center (BMC), Cell Biology, Ludwig-Maximilians-Universitat Munchen, Munich, Germany. Munich Cluster for Systems Neurology (SyNergy), Munich, Germany. BioMedical Center (BMC), Biochemistry, Ludwig-Maximilians-Universitat Munchen, Munich, Germany. German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany. Department of Neurology, Ulm University, Ulm, Germany. Department of Neurology, Harvard Medical School, Massachusetts General Hospital, Charlestown, MA, 02129, USA. Broad Institute of Harvard University and MIT, Cambridge, MA, 02142, USA. Molecular Neurogenetics Laboratory, Max Planck Institute for Molecular Biomedicine, Muenster, Germany. erik.storkebaum@mpi-muenster.mpg.de. Faculty of Medicine, University of Muenster, Muenster, Germany. erik.storkebaum@mpi-muenster.mpg.de. Inserm, UMR-S1118, 67085, Strasbourg, France. ldupuis@unistra.fr. Faculte de Medecine, UMR-S1118, Universite de Strasbourg, 67085, Strasbourg, France. ldupuis@unistra.fr.
Identifiers:ISSN:1432-0533 (Electronic) 0001-6322 (Linking) %R 10.1... [ID No:1]
URL:https://www.ncbi.nlm.nih.gov/pubmed/28243725 [ID No:2]
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.