Literature DB >> 1525714

Ocular-chondrodysplasia in labrador retriever dogs: a morphometric and electron microscopical analysis.

C E Farnum1, K Jones, R Riis, N J Wilsman.   

Abstract

Ocular-chondrodysplasia in Labrador Retriever dogs is characterized by short-limbed dwarfism and ocular abnormalities. The purposes of the present study were to develop morphological criteria to define the matrix and/or chondrocytic abnormalities associated with this chondrodysplasia, and to test the hypothesis that ineffective matrix-directed cellular swelling was associated with the decreased longitudinal bone growth in these animals. The proximal and distal radial growth plates were collected from four affected animals of the same litter. Stereological techniques were used to analyze both cellular shapes and cellular volume changes in the hypertrophic zone. The pathological changes seen in these growth plates varied between animals and included disorganization of cellular columns with abnormal extent of calcification. Chondrocytes of all zones contained two types of abnormal cellular inclusions classified as light and dark, based on the intensity of eosinophilic staining. Both types of inclusions contained material that resembled the surrounding extracellular matrix, varying only in the apparent hydration of the contents. It could be demonstrated that light inclusions were located in the peripheral cytoplasm and connected to the extracellular matrix through narrow channels. By contrast, dark inclusions were membrane bound and perinuclear. Chondrocytes with multiple, large inclusions appeared to be undergoing degenerative changes. Although the final volume achieved by hypertrophic chondrocytes was consistent with that of normal growth plates, there was a high level of variability of chondrocytic shape and evidence of premature cellular condensation in the maturation zone. The severity of the dwarfism correlated both with the extent of chondrocytic changes and the severity of the ocular lesions.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1525714     DOI: 10.1007/bf00582173

Source DB:  PubMed          Journal:  Calcif Tissue Int        ISSN: 0171-967X            Impact factor:   4.333


  36 in total

1.  Physiological mechanisms adopted by chondrocytes in regulating longitudinal bone growth in rats.

Authors:  E B Hunziker; R K Schenk
Journal:  J Physiol       Date:  1989-07       Impact factor: 5.182

2.  Stereology for anisotropic cells: application to growth cartilage.

Authors:  L M Cruz-Orive; E B Hunziker
Journal:  J Microsc       Date:  1986-07       Impact factor: 1.758

3.  Cellular stages in cartilage formation as revealed by morphometry, radioautography and type II collagen immunostaining of the mandibular condyle from weanling rats.

Authors:  H U Luder; C P Leblond; K von der Mark
Journal:  Am J Anat       Date:  1988-07

4.  Spondyloepiphyseal dysplasia, chondroitin sulfate type: a possible defect of PAPS--chondroitin sulfate sulfotransferase in humans.

Authors:  P A Mourão; S Kato; P V Donnelly
Journal:  Biochem Biophys Res Commun       Date:  1981-01-30       Impact factor: 3.575

5.  Structural and functional comparison of type IX collagen-proteoglycan from chicken cartilage and vitreous humor.

Authors:  R G Brewton; D W Wright; R Mayne
Journal:  J Biol Chem       Date:  1991-03-15       Impact factor: 5.157

6.  Immunochemical and immunocytochemical studies of the C-propeptide of type II procollagen in chondrocytes of the growth plate.

Authors:  E R Lee; Y Matsui; A R Poole
Journal:  J Histochem Cytochem       Date:  1990-05       Impact factor: 2.479

7.  Vitreoretinal degeneration as a sign of generalized connective tissue diseases.

Authors:  I H Maumenee
Journal:  Am J Ophthalmol       Date:  1979-09       Impact factor: 5.258

8.  Identification of the molecular defect in a family with spondyloepiphyseal dysplasia.

Authors:  B Lee; H Vissing; F Ramirez; D Rogers; D Rimoin
Journal:  Science       Date:  1989-05-26       Impact factor: 47.728

9.  Improved cartilage fixation by ruthenium hexammine trichloride (RHT). A prerequisite for morphometry in growth cartilage.

Authors:  E B Hunziker; W Herrmann; R K Schenk
Journal:  J Ultrastruct Res       Date:  1982-10

10.  Cellular turnover at the chondro-osseous junction of growth plate cartilage: analysis by serial sections at the light microscopical level.

Authors:  C E Farnum; N J Wilsman
Journal:  J Orthop Res       Date:  1989       Impact factor: 3.494

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