The role of intracellular calcium phosphate in osteoblast-mediated bone apatite formation
Open accessAbstract
Mineralization is a ubiquitous process in the animal kingdom and is fundamental to human development and health. Dysfunctional or aberrant mineralization leads to a variety of medical problems, and so an understanding of these processes is essential to their mitigation. Osteoblasts create the nano-composite structure of bone by secreting a collagenous extracellular matrix (ECM) on which apatite crystals subsequently form. However, despite their requisite function in building bone and decades of observations describing intracellular calcium phosphate, the precise role osteoblasts play in mediating bone apatite formation remains largely unknown. To better understand the relationship between intracellular and extracellular mineralization, we combined a sample-preparation method that simultaneously preserved mineral, ions, and ECM with nano-analytical electron microscopy techniques to examine osteoblasts in an in vitro model of bone formation. We identified calcium phosphate both within osteoblast mitochondrial granules and intracellular vesicles that transported material to the ECM. Moreover, we observed calcium-containing vesicles conjoining mitochondria, which also contained calcium, suggesting a storage and transport mechanism. Our observations further highlight the important relationship between intracellular calcium phosphate in osteoblasts and their role in mineralizing the ECM. These observations may have important implications in deciphering both how normal bone forms and in understanding pathological mineralization.
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In 2012, electron-dense, noncrystalline, Ca- and P-rich granules were identified within, and possibly being transferred from, osteoblastic cell culture mitochondria processed with high-pressure freezing and freeze substitution.
“However, in 2012, electron-dense, noncrystalline, Ca- and P-rich granules were identified within, and possibly being transferred from, osteoblastic cell culture mitochondria processed with high-pressure freezing (HPF) and freeze substitution (FS) [131].”
From A Review of Phosphate Mineral Nucleation in Biology and Geobiology (2013) · cites this paper as [131]
Cryo-EM and HPF-FS preparation have recently provided evidence of a secretory process for bone mineralization.
“Cryo-EM and HPF-FS preparation have recently provided evidence of a secretory process for bone mineralization [131, 133, 154, 155].”
From A Review of Phosphate Mineral Nucleation in Biology and Geobiology (2013) · cites this paper as [131]
Boonrungsiman et al. observed Ca- and P-rich mitochondrial granules within mineralizing murine osteoblast cultures and presented evidence of vesicle-mitochondrial interactions with high angle-annular dark-field scanning TEM of samples prepared with high-pressure freezing and freeze substitution.
“Boonrungsiman et al. [131] observed Ca- and P-rich mitochondrial granules within mineralizing murine osteoblast cultures, and presented evidence of vesicle–mitochondrial interactions with high angle-annular dark-field scanning TEM of samples prepared with high-pressure freezing and freeze substitution (HPF-FS) (Fig. 3).”
From A Review of Phosphate Mineral Nucleation in Biology and Geobiology (2013) · cites this paper as [131]
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Transformation of amorphous calcium phosphate to bone-like apatite
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- Authors
- Boonrungsiman, S., Gentleman, E., Carzaniga, R., Evans, N. D., McComb, D. W., Porter, A. E., & Stevens, M. M.
- Affiliations
- Imperial College London (GB)
- King's College London (GB)
- Institute of Biomedical Engineering (Japan) (JP)
- The Ohio State University (US)
- Departments of aMaterials and
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-07-24
- Volume
- 109
- Issue
- 35
- Pages
- 14170-14175
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3435222
- OpenAlex
- W2001923641
- Cited by
- 568
- References
- 4
- Citations by year
- 2026: 22 · 2025: 48 · 2024: 48 · 2023: 44 · 2022: 40 · 2021: 59 · 2020: 55 · 2019: 40 · 2018: 49 · 2017: 37 · 2016: 37 · 2015: 32 · 2014: 31 · 2013: 18 · 2012: 6
- FWCI
- 22.33
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- ePrints Soton (University of Southampton) (acceptedVersion)
- Research Portal (King's College London) (submittedVersion, other-oa)
- Funders
- Wellcome Trust (093687)
- European Commission
- Medical Research Council
- FP7 Ideas: European Research Council (257182)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Alkaline Phosphatase Research Studies
- Health Sciences › Medicine › Rheumatology › Bone and Dental Protein Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Keywords
- osteoblasts, bone mineralization, extracellular matrix mineralization, mitochondrial granules, intracellular vesicles, calcium transport, pathological mineralization, bone formation
- MeSH terms
- Age Factors, Animals, Animals, Newborn, Apatites, Biological Transport, Calcification, Physiologic, Calcium Phosphates, Crystallization, Extracellular Matrix, Mitochondria, Osteoblasts, Skull, Cytoplasmic Vesicles, Microscopy, Electron, Transmission, Spectroscopy, Electron Energy-Loss, Mice
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