ArticleThe Histochemical journal1997
The ultrastructure of slam-frozen bone mineral.
Article in The Histochemical journal, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 25 citations in OpenAlex.
- Stimulation of Metabolic Activity and Cell Differentiation in Osteoblastic and Human Mesenchymal Stem Cells by a Nanohydroxyapatite Paste Bone Graft Substitute.Materials (Basel, Switzerland) · 2022Article
- Nanoscale Strontium-Substituted Hydroxyapatite Pastes and Gels for Bone Tissue Regeneration.Nanomaterials (Basel, Switzerland) · 2021Article
- Rapid Mix Preparation of Bioinspired Nanoscale Hydroxyapatite for Biomedical Applications.Journal of visualized experiments : JoVE · 2017Article
- Mapping amorphous calcium phosphate transformation into crystalline mineral from the cell to the bone in zebrafish fin rays.Proceedings of the National Academy of Sciences of the United States of America · 2010Article
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- Cryopreservation and image enhancement of juvenile and adult dentine mineral.The Histochemical journal · 2000Article
- Calcified microspheres as biological entities and their isolation from bone.The Histochemical journal · 1999Article
- Evidence for phosphoprotein microspheres in bone.The Histochemical journal · 1998Article
Corrections and comments
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Authors and funding
3 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Bone salt may be altered by preparative procedures. 'Slam' freezing can usefully be applied to bone mineral because it minimizes preparation and preserves the tissue chemistry. The structure and composition of the mineral in 'slam'-frozen neonatal mouse calvaria (which require neither previous slicing nor manipulation) was examined by transmission electron microscopy and X-ray microanalysis in unstained sections, 0.25 micron thick (i.e. unusually thick). Comparison was made with fresh intact calvaria and with 'snap'-frozen histological sections of mature rat femora. Under the optical microscope, calcified microspheres, up to 1 micron in diameter, were evident within 'young' osteocytes and within the extracellular matrix of both immature and mature, unstained and von Kossa-stained bone. In the electron microscope, microspheres of similar dimension and distribution were observed after 'slam' freezing and were divided into two groups. One group, found inside and outside cells, had a substructure of closely packed, electron-dense, rounded bodies 30-40 nm in diameter; despite their unusual stability in EDTA, X-ray microanalysis indicated high levels of both calcium and phosphorus. The other group was found at the calcification front and, although similar to the first group in size and chemical composition, these microspheres had a substructure of clusters of 5-nm-thick electron-dense filaments containing mineral that was characteristically EDTA labile. The 30- to 40-nm dense bodies did not appear to be mitochondrial and were absent from customary fixed and resin-embedded, ultrathin, stained preparations. They were not observed singly and their aggregation into arrangements of microspheres, sometimes linked by bridges, may be an important preliminary step in the development of the filamentous clusters. Needle-shaped and plate-like crystals of bone mineral were absent. It was concluded that 'slam' freezing preserves both intracellular and extracellular bone salt in the form of microspheres within which the mineral may modulate from dense bodies into filamentous arrays of variable density with maturity.
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