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|Title:||Delayed development of ossification centers in the tibia of prenatal and early postnatal MPS VII mice|
|Citation:||Molecular Genetics and Metabolism, 2018; 124(2):135-142|
|Zhirui Jiang, Ainslie L.K. Derrick-Roberts, Matilda R. Jackson, Charné Rossouw, Carmen E. Pyragius, Cory Xian, Janice Fletcher, Sharon Byers|
|Abstract:||Short stature is a characteristic feature of most of the mucopolysaccharidoses, a group of inherited lysosomal storage disorders caused by a single enzyme deficiency. MPS patients present with progressive skeletal defects from an early age, including short stature due to impaired cartilage-to-bone conversion (endochondral ossification). The aim of this study was to determine which murine MPS model best reproduces the bone length reduction phenotype of human MPS and use this model to determine the earliest developmental stage when disrupted endochondral ossification first appears. Gusmps/mps mice representing severe MPS VII displayed the greatest reduction in bone elongation and were chosen for histopathological analysis. Tibial development was assessed from E12.5 to 6 months of age. Chondrocytes in the region of the future primary ossification center became hypertrophic at a similar age to normal in the MPS VII mouse fetus, but a delay in bone deposition was observed with an approximate 1 day delay in the formation of the primary ossification centre. Likewise, chondrocytes in the region of the future secondary ossification center also became hypertrophic at the same age as normal in the MPS VII early postnatal mouse. Bone deposition in the secondary ossification centre was delayed by two days in the MPS VII proximal tibia (observed at postnatal day 14 (P14) compared to P12 in normal). The thickness of the tibial growth plate was larger in MPS VII mice from P9 onwards. Abnormal endochondral ossification starts in utero in MPS VII and worsens with age. It is characterized by a normal timeframe for chondrocyte hypertrophy but a delay in the subsequent deposition of bone in both the primary and secondary ossification centres, accompanied by an increase in growth plate thickness. This suggests that the signals for vascular invasion and bone deposition, some of which are derived from hypertrophic chondrocytes, are altered in MPS VII.|
|Keywords:||Endochondral ossification; Growth plate; Mucopolysaccharidosis; Murine models; Primary ossification center; Secondary ossification center; Short stature|
|Rights:||Crown Copyright © 2018 Published by Elsevier Inc. All rights reserved.|
|Appears in Collections:||Genetics publications|
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