Literature DB >> 7757284

Retarded bone formation in GM1-gangliosidosis: a study of the infantile form and comparison with two canine models.

J Alroy1, K Knowles, S H Schelling, E M Kaye, A E Rosenberg.   

Abstract

The development of skeletal lesions in two canine models of GM1-gangliosidosis, English springer spaniels and Portuguese water dogs, has been studied and compared to osseous abnormalities in a child with the infantile form of the disease. In the canine models, skeletal dysplasia was progressive. Lesions were noted at 2 months of age and characterized by retarded endochondral ossification and osteoporosis. Older puppies had focal cartilage necrosis within lumbar vertebral epiphyses. At the cellular level, lesions were characterized by chondrocytic hypertrohy and lysosomal accumulation of storage compounds. Our studies illustrate that the skeletal lesions in both canine models are similar to those in a child with GM1-gangliosidosis. Furthermore, we proposed that the abnormal storage of partially degraded compounds in affected chondrocytes might explain, at least in part, the retarded bone formation noted in patients with GM1-gangliosidosis.

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Year:  1995        PMID: 7757284     DOI: 10.1007/BF00192635

Source DB:  PubMed          Journal:  Virchows Arch        ISSN: 0945-6317            Impact factor:   4.064


  24 in total

Review 1.  Cartilage collagens. What is their function, and are they involved in articular disease?

Authors:  R Mayne
Journal:  Arthritis Rheum       Date:  1989-03

2.  Aberrant composition of chondroitin sulfates in the cartilage-type proteoglycan isolated from the iliac crest of patients with some lysosomal storage diseases.

Authors:  A Oohira; F Matsui; H Nogami
Journal:  J Biochem       Date:  1986-05       Impact factor: 3.387

3.  Specific inhibition of type I and type II collagen fibrillogenesis by the small proteoglycan of tendon.

Authors:  K G Vogel; M Paulsson; D Heinegård
Journal:  Biochem J       Date:  1984-11-01       Impact factor: 3.857

4.  Abnormal dermal proteoglycan in aspartylglycosaminuria: a possible mechanism for ultrastructural changes of collagen fibrils in a glycoprotein storage disorder.

Authors:  K Näntö-Salonen; H Larjava; A M Säämanen; J Heino; R Penttinen; L J Pelliniemi; M Tammi
Journal:  Connect Tissue Res       Date:  1987       Impact factor: 3.417

5.  Diagnosis of unsuspected fetal metabolic storage disease by routine placental examination.

Authors:  D J Roberts; M G Ampola; J M Lage
Journal:  Pediatr Pathol       Date:  1991 Jul-Aug

6.  Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorder.

Authors:  K Näntö-Salonen; L J Pelliniemi; S Autio; T Kivimäki; J Rapola; R Penttinen
Journal:  Lab Invest       Date:  1984-10       Impact factor: 5.662

7.  S-100 protein and neuron specific enolase immunoreactivity of normal, hyperplastic and neoplastic chondrocytes in relation to the composition of the extracellular matrix.

Authors:  V Karabela-Bouropoulou; S Markaki; C Milas
Journal:  Pathol Res Pract       Date:  1988-11       Impact factor: 3.250

8.  Study of the bone pathology in early mucolipidosis II (I-cell disease).

Authors:  U E Pazzaglia; G Beluffi; E Bianchi; A Castello; A Coci; A Marchi
Journal:  Eur J Pediatr       Date:  1989-04       Impact factor: 3.183

9.  Skeletal complications of Gaucher disease.

Authors:  D W Stowens; S L Teitelbaum; A J Kahn; J A Barranger
Journal:  Medicine (Baltimore)       Date:  1985-09       Impact factor: 1.889

10.  The pathology of the feline model of mucopolysaccharidosis VI.

Authors:  M E Haskins; G D Aguirre; P F Jezyk; D F Patterson
Journal:  Am J Pathol       Date:  1980-12       Impact factor: 4.307

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  4 in total

1.  The skeletal phenotype of intermediate GM1 gangliosidosis: Clinical, radiographic and densitometric features, and implications for clinical monitoring and intervention.

Authors:  Carlos R Ferreira; Debra S Regier; Robin Yoon; Kristen S Pan; Jean M Johnston; Sandra Yang; Jürgen W Spranger; Cynthia J Tifft
Journal:  Bone       Date:  2019-11-06       Impact factor: 4.398

2.  An in vitro model for abnormal skeletal development in the lysosomal storage diseases.

Authors:  A L Aulthouse; J Alroy
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064

3.  Impaired elastic-fiber assembly by fibroblasts from patients with either Morquio B disease or infantile GM1-gangliosidosis is linked to deficiency in the 67-kD spliced variant of beta-galactosidase.

Authors:  A Hinek; S Zhang; A C Smith; J W Callahan
Journal:  Am J Hum Genet       Date:  2000-06-06       Impact factor: 11.025

4.  Insights into post-translational processing of beta-galactosidase in an animal model resembling late infantile human G-gangliosidosis.

Authors:  R Kreutzer; M Kreutzer; M J Pröpsting; A C Sewell; T Leeb; H Y Naim; W Baumgärtner
Journal:  J Cell Mol Med       Date:  2007-12-14       Impact factor: 5.310

  4 in total

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