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  Neurofibromin (Nf1) is required for skeletal muscle development

Kossler, N., Stricker, S., Rodelsperger, C., Robinson, P. N., Kim, J., Dietrich, C., et al. (2011). Neurofibromin (Nf1) is required for skeletal muscle development. Hum Mol Genet, 20(14), 2697-709. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/21478499 http://hmg.oxfordjournals.org/content/20/14/2697.full.pdf.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0010-783C-A Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0010-783D-8
Genre: Journal Article

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 Creators:
Kossler, N.1, Author              
Stricker, S.1, Author              
Rodelsperger, C.1, Author              
Robinson, P. N.1, Author              
Kim, J., Author
Dietrich, C., Author
Osswald, M.1, Author              
Kuhnisch, J., Author
Stevenson, D. A., Author
Braun, T., Author
Mundlos, S.1, Author              
Kolanczyk, M.1, Author              
Affiliations:
1Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433557              

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Free keywords: Animals; Bone Diseases, Developmental/genetics/metabolism/pathology; Cell Differentiation/*physiology; *Cell Proliferation; Humans; Mice; Mice, Transgenic; Muscle Development/*physiology; Muscle, Skeletal/*metabolism/pathology; Muscular Dystrophies/genetics/metabolism/pathology; Mutation; Myoblasts, Skeletal/*metabolism/pathology; Neurofibromatosis 1/genetics/metabolism/pathology; Neurofibromin 1/genetics/*metabolism; Satellite Cells, Skeletal Muscle/metabolism/pathology; Scoliosis/genetics/metabolism/pathology
 Abstract: Neurofibromatosis type 1 (NF1) is a multi-system disease caused by mutations in the NF1 gene encoding a Ras-GAP protein, neurofibromin, which negatively regulates Ras signaling. Besides neuroectodermal malformations and tumors, the skeletal system is often affected (e.g. scoliosis and long bone dysplasia) demonstrating the importance of neurofibromin for development and maintenance of the musculoskeletal system. Here, we focus on the role of neurofibromin in skeletal muscle development. Nf1 gene inactivation in the early limb bud mesenchyme using Prx1-cre (Nf1(Prx1)) resulted in muscle dystrophy characterized by fibrosis, reduced number of muscle fibers and reduced muscle force. This was caused by an early defect in myogenesis affecting the terminal differentiation of myoblasts between E12.5 and E14.5. In parallel, the muscle connective tissue cells exhibited increased proliferation at E14.5 and an increase in the amount of connective tissue as early as E16.5. These changes were accompanied by excessive mitogen-activated protein kinase pathway activation. Satellite cells isolated from Nf1(Prx1) mice showed normal self-renewal, but their differentiation was impaired as indicated by diminished myotube formation. Our results demonstrate a requirement of neurofibromin for muscle formation and maintenance. This previously unrecognized function of neurofibromin may contribute to the musculoskeletal problems in NF1 patients.

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 Dates: 2011
 Publication Status: Published in print
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Title: Hum Mol Genet
Source Genre: Journal
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Pages: - Volume / Issue: 20 (14) Sequence Number: - Start / End Page: 2697 - 709 Identifier: ISSN: 1460-2083 (Electronic) 0964-6906 (Linking)