Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome

• Published in: Journal of bone and mineral research Vol. 31; no. 11; pp. 1930 - 1942
• Main Authors: Gistelinck, Charlotte, Witten, Paul Eckhard, Huysseune, Ann, Symoens, Sofie, Malfait, Fransiska, Larionova, Daria, Simoens, Pascal, Dierick, Manuel, Van Hoorebeke, Luc, De Paepe, Anne, Kwon, Ronald Y, Weis, MaryAnn, Eyre, David R, Willaert, Andy, Coucke, Paul J
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.11.2016
• Subjects: Amino Acid Sequence; Animals; Arthrogryposis - complications; Arthrogryposis - diagnostic imaging; Arthrogryposis - metabolism; Arthrogryposis - pathology; Bone and Bones - abnormalities; Bone and Bones - diagnostic imaging; Bone and Bones - pathology; BRUCK SYNDROME; Calcification, Physiologic; Catalytic Domain; Codon, Nonsense - genetics; COLLAGEN; Collagen Type I - metabolism; Conserved Sequence - genetics; Cross-Linking Reagents - metabolism; Danio rerio; Evolution, Molecular; Hydroxylation; Larva - metabolism; Lysine - metabolism; LYSYL HYDROXYLASE 2; Mass Spectrometry; Musculoskeletal Abnormalities - complications; Musculoskeletal Abnormalities - diagnostic imaging; Musculoskeletal Abnormalities - metabolism; Musculoskeletal Abnormalities - pathology; Notochord - pathology; OSTEOGENESIS IMPERFECTA; Osteogenesis Imperfecta - complications; Osteogenesis Imperfecta - diagnostic imaging; Osteogenesis Imperfecta - metabolism; Osteogenesis Imperfecta - pathology; Peptides - metabolism; Phenotype; PLOD2; X-Ray Microtomography; Zebrafish - metabolism; Zebrafish Proteins - genetics; OSTEOGENESIS IMPERFECTA; PLOD2; COLLAGEN; LYSYL HYDROXYLASE 2; BRUCK SYNDROME
• ISSN: 0884-0431; 1523-4681
• DOI: 10.1002/jbmr.2977

ABSTRACT Bruck syndrome (BS) is a disorder characterized by joint flexion contractures and skeletal dysplasia that shows strong clinical overlap with the brittle bone disease osteogenesis imperfecta (OI). BS is caused by biallelic mutations in either the FKBP10 or the PLOD2 gene. PLOD2 encodes the lysyl hydroxylase 2 (LH2) enzyme, which is responsible for the hydroxylation of lysine residues in fibrillar collagen telopeptides. This hydroxylation directs crosslinking of collagen fibrils in the extracellular matrix, which is necessary to provide stability and tensile integrity to the collagen fibrils. To further elucidate the function of LH2 in vertebrate skeletal development, we created a zebrafish model harboring a homozygous plod2 nonsense mutation resulting in reduced telopeptide hydroxylation and crosslinking of bone type I collagen. Adult plod2 mutants present with a shortened body axis and severe skeletal abnormalities with evidence of bone fragility and fractures. The vertebral column of plod2 mutants is short and scoliotic with compressed vertebrae that show excessive bone formation at the vertebral end plates, and increased tissue mineral density in the vertebral centra. The muscle fibers of mutant zebrafish have a reduced diameter near the horizontal myoseptum. The endomysium, a layer of connective tissue ensheathing the individual muscle fibers, is enlarged. Transmission electron microscopy of mutant vertebral bone shows type I collagen fibrils that are less organized with loss of the typical plywood‐like structure. In conclusion, plod2 mutant zebrafish show molecular and tissue abnormalities in the musculoskeletal system that are concordant with clinical findings in BS patients. Therefore, the plod2 zebrafish mutant is a promising model for the elucidation of the underlying pathogenetic mechanisms leading to BS and the development of novel therapeutic avenues in this syndrome. © 2016 American Society for Bone and Mineral Research.