Morphological and functional features of clasts in low phosphate, vitamin D-deficiency rickets

Citation
J. Nordahl et al., Morphological and functional features of clasts in low phosphate, vitamin D-deficiency rickets, CALCIF TIS, 67(5), 2000, pp. 400-407
Citations number
32
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
CALCIFIED TISSUE INTERNATIONAL
ISSN journal
0171967X → ACNP
Volume
67
Issue
5
Year of publication
2000
Pages
400 - 407
Database
ISI
SICI code
0171-967X(200011)67:5<400:MAFFOC>2.0.ZU;2-C
Abstract
Focusing on resorption processes, we have extended our previous studies on chondroclasts and osteoclasts in normally developing tissues, using a model of nutritionally induced vitamin D-deficiency rickets. To analyze the reso rption process, we investigated the matrix-resorbing cells in this modified and poorly mineralized tissue regarding morphological features and express ion of tartrate-resistant acid phosphatase (TRAP) at the subcellular level. Our goal was to test the hypotheses that initiation of resorption is impai red with unmineralized matrix, and that such alterations involve changes in the subcellullar distribution of TRAP, implicating a role for this enzyme in the resorption process. Our results reveal distinctly different morpholo gical appearances of clast-like cells in rickets compared with normal osteo clasts and chondroclasts. Ordinary resorption structures of osteoclasts and chondroclasts at the cell-matrix border, i.e., ruffled borders and clear z ones, are profoundly altered in favor of a less well-defined intermediate z one. TRAP distribution at the subcellullar level is also clearly different from that in osteoclasts and chondroclasts from normal rodents, with impair ed secretion; consequently, the enzyme is unable to function in the matrix outside the ruffled border. Our ultrastructural observations demonstrate th at in rickets, the clasts are incapable of degrading the poorly mineralized cartilage and bone efficiently. Rachitic clasts seem to be recruited to th e matrix surface and interaction between cell and matrix is also initiated, but definitive resorption structures at the cell-matrix border are not nor mally developed. Whether resorption is inhibited by the mere lack of minera l or mineral-associated proteins, or by other mechanisms remains to be sett led.