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Material and mechanical properties of bones deficient for fibrillin-1 or fibrillin-2 microfibrils
Authors:Emilio Arteaga-Solis  Lee Sui-ArteagaMinwook Kim  Mitchell B. Schaffler  Karl J. JepsenNancy Pleshko  Francesco Ramirez
Affiliation:
  • a Department of Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, One Gustave L Levy Place, Box 1603, New York, NY 10029, USA
  • b McKay Orthopaedic Research Laboratory, University of Pennsylvania, 3451 Walnut Street, Philadelphia, PA 19104, USA
  • c Department of Orthopedics, Mount Sinai School of Medicine, One Gustave L Levy Place, Box 1603, New York, NY 10029, USA
  • d Department of Mechanical Engineering, Temple University, 1801 N Broad Street, Philadelphia, PA 19122, USA
  • Abstract:The contribution of non-collagenous components of the extracellular matrix to bone strength is largely undefined. Here we report that deficiency of fibrillin-1 or fibrillin-2 microfibrils causes distinct changes in bone material and mechanical properties. Morphometric examination of mice with hypomorphic or null mutations in fibrillin-1 or fibrillin-2, respectively, revealed appreciable differences in the postnatal shaping and growth of long bones. Fourier transform infrared imaging spectroscopy indicated that fibrillin-1 plays a predominantly greater role than fibrillin-2 in determining the material properties of bones. Biomechanical tests demonstrated that fibrillin-2 exerts a greater positive influence on the mechanical properties of bone than fibrillin-1 assemblies. Published evidence indirectly supports the notion that the above findings are mostly, if not exclusively, related to the differential control of TGFβ family signaling by fibrillin proteins. Our study therefore advances our understanding of the role that extracellular microfibrils play in bone physiology and implicitly, in the pathogenesis of bone loss in human diseases caused by mutations in fibrillin-1 or -2.
    Keywords:Bone material and mechanical properties   Congenital contractural arachnodactyly   Fibrillin   Marfan syndrome   TGFβ
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