Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Osteogenesis imperfecta (OI) is a heritable disorder, in both a dominant and recessive manner, of connective tissue characterized by brittle bones, fractures and extraskeletal manifestations. How structural mutations of type I collagen (dominant OI) or of its post-translational modification machinery (recessive OI) can cause abnormal quality and quantity of bone is poorly understood. Notably, the clinical overlap between dominant and recessive forms of OI suggests common molecular pathomechanisms. Here, we show that excessive transforming growth factor-β (TGF-β) signaling is a mechanism of OI in both recessive (Crtap(-/-)) and dominant (Col1a2(tm1.1Mcbr)) OI mouse models. In the skeleton, we find higher expression of TGF-β target genes, higher ratio of phosphorylated Smad2 to total Smad2 protein and higher in vivo Smad2 reporter activity. Moreover, the type I collagen of Crtap(-/-) mice shows reduced binding to the small leucine-rich proteoglycan decorin, a known regulator of TGF-β activity. Anti-TGF-β treatment using the neutralizing antibody 1D11 corrects the bone phenotype in both forms of OI and improves the lung abnormalities in Crtap(-/-) mice. Hence, altered TGF-β matrix-cell signaling is a primary mechanism in the pathogenesis of OI and could be a promising target for the treatment of OI.

Original publication

DOI

10.1038/nm.3544

Type

Journal article

Journal

Nature medicine

Publication Date

06/2014

Volume

20

Pages

670 - 675

Addresses

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.

Keywords

Animals, Mice, Inbred C57BL, Mice, Knockout, Mice, Osteogenesis Imperfecta, Collagen Type I, Transforming Growth Factor beta, Proteins, Molecular Chaperones, Extracellular Matrix Proteins, Immunoblotting, Electrophoresis, Polyacrylamide Gel, Surface Plasmon Resonance, Analysis of Variance, Signal Transduction, Female, Mass Spectrometry, X-Ray Microtomography, Real-Time Polymerase Chain Reaction