Skeletal muscle pathology in Costello and cardio-facio-cutaneous syndromes: developmental consequences of germline Ras/MAPK activation on myogenesis.

Abstract

Cardio-facio-cutaneous syndrome (CFC) and Costello syndrome (CS) are two of the more rare RASopathies caused by altered signal transduction of the Ras/mitogen-activated protein kinase (MAPK) pathway. All of the RASopathies exhibit some degree of hypotonia, but CS and CFC are more severe. To determine if individuals with CS and CFC have an underlying skeletal myopathy, we systematically evaluated skeletal muscle pathology in both conditions. We reviewed pathology reports from six individuals who had undergone a skeletal muscle biopsy, and we reviewed histology slides on two cases with CS and one case with CFC. All patients in the cohort had histopathologic findings, and two consistent abnormalities were identified. The first was the presence of abnormal muscle fiber size and variability, and the second was the presence of type 2 fiber predominance. Given the degree of hypotonia typically present in these patients, the overall architecture of the muscle was relatively normal, without showing indications of severe structural histopathology or metabolic abnormalities. Because the Ras/MAPK pathway is vital for skeletal myogenesis, we evaluated the effects of CS and CFC mutations on myogenesis using C2C12 myoblasts. All CS/CFC mutations inhibited myoblast differentiation as indicated by fewer myosin heavy chain expressing cells and a decrease in the number of myotubes as compared to controls. These findings indicate that CS and CFC may have a true myopathy related to an inherent dysregulation of skeletal myogenesis, which further expands our understanding of the consequences of germline Ras/MAPK mutations.

• Authors: William E Tidyman, Han S Lee, Katherine A Rauen
• Journal: American journal of medical genetics. Part C, Seminars in medical genetics (Am J Med Genet C Semin Med Genet) Vol. 157C Issue 2 Pg. 104-14 (May 15 2011) ISSN: 1552-4876 [Electronic] United States
• PMID: 21495178 (Publication Type: Journal Article)
• Copyright: 2011 Wiley-Liss, Inc.

Chemical References

• Proto-Oncogene Proteins p21(ras)

Topics

• Child
• Child, Preschool
• Cohort Studies
• Costello Syndrome (genetics, pathology)
• Ectodermal Dysplasia (genetics, pathology)
• Facies
• Failure to Thrive (genetics, pathology)
• Female
• Germ Cells (metabolism)
• Heart Defects, Congenital (genetics, pathology)
• Histological Techniques
• Humans
• Infant
• Male
• Muscle Development (physiology)
• Muscle, Skeletal (pathology)
• Mutation (genetics)
• Plasmids (genetics)
• Proto-Oncogene Proteins p21(ras) (metabolism)
• Signal Transduction (genetics)