Multinucleated cells formed on calcified dentine from mouse bone marrow cells treated with 1α,25‐dihydroxyvitamin D3 have ruffled borders and resorb dentine
- 1 July 1989
- journal article
- research article
- Published by Wiley in The Anatomical Record
- Vol. 224 (3) , 379-391
- https://doi.org/10.1002/ar.1092240307
Abstract
Osteoclast-like multinucleated cells were formed from mouse bone marrow mononuclear cells, and their morphology on coverslips and on calcified dentine slices was compared by means of transmission electron microscopy. Addition of 1α,25-dihydroxyvitamin D3 [1α,25(OH)2D3] to bone marrow cells cultured on coverslips greatly stimulated the formation of multinucleated cells within 8 days. These multinucleated cells had the cytological features of osteoclasts (abundant pleomorphic mitochondria, a large number of vacuoles and lysosomes, many stacks of Golgi membranes, and an extensive canalicular system), but they developed neither ruffled borders nor clear zones. The multinucleated cells appeared to result from direct fusion of mononuclear progenitor cells, whose structural features were similar to those of multinucleated cells. Like isolated osteoclasts, both multinucleated cells and their precursors exhibited an intense reaction for tartrate-resistant acid phosphatase (TRACP) in the cisterns of endoplasmic reticulum and lysosomes. Multinucleated cells formed from alveolar macrophages in the presence of 1α,25(OH)2D3 were totally negative for TRACP reaction. When marrow cells were cultured on dentine slices in the presence of 1α,25(OH)2D3, some of the multinucleated cells were located in the shallow resorption lacunae of dentine surfaces, and they developed the characteristic ruffled borders and clear zones. The narrow extracellular spaces of the ruffled borders, the adjacent pale endocytotic vacuoles, and the dark lysosomes located in the perinuclear cytoplasm of the multinucleated cells contained numerous apatite crystals delete in resorption lacunae. These results indicate that (1) the multinucleated cells formed on coverslips from mouse marrow cells treated with 1α,25(OH)2D3 exhibit non-functional basic features of osteoclast morphology, and (2) differentiation of the multinucleated cells into functional osteoclasts requires some components of calcified dentine.This publication has 29 references indexed in Scilit:
- Hormonal regulation of acid phosphatase release by osteoclasts disaggregated from neonatal rat boneJournal of Cellular Physiology, 1987
- Isolated osteoclasts resorb the organic and inorganic components of bone.The Journal of cell biology, 1986
- Activity and distribution of lysosomal enzymes during collagenous matrix-induced cartilage, bone, and bone marrow developmentDevelopmental Biology, 1981
- New Knowledge on the Origin, Function and Fate of OsteoclastsPublished by Wolters Kluwer Health ,1981
- Direct in vivo demonstration by radioautography of specific binding sites for calcitonin in skeletal and renal tissues of the rat.The Journal of cell biology, 1980
- Demonstration of lysosomal and extralysosomal sites for acid phosphatase in mouse kidney tubule cells with p-nitrophenylphosphate lead-salt technique.Journal of Histochemistry & Cytochemistry, 1975
- The organic-inorganic relationships in bone matrix undergoing osteoclastic resorptionCalcified Tissue International, 1974
- Enzymatic and electron microscopic analysis of isolated osteoclastsCalcified Tissue International, 1972
- Electron microscopic localization of hydrolytic enzymes in osteoclastsJournal of Molecular Histology, 1972