Rowe · Journal of periodontology 1999 · in vitro comparative cell culture study · n=?

Enhanced production of mineralized nodules and collagenous proteins in vitro by calcium ascorbate supplemented with vitamin C metabolites.

Cited 22 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

In vitro bench study evaluating cell cultures without clinical or in vivo human trials.

PubMed 10505801 · doi:10.1902/jop.1999.70.9.992 · record verified 2026-08-31

What was done

Cells harvested from expanded polytetrafluoroethylene (ePTFE) membranes used in edentulous ridge augmentation were cultured in vitro for 2 to 5 weeks with beta-glycerophosphate and either unsupplemented calcium ascorbate, calcium ascorbate containing vitamin C metabolites, or ascorbate spiked with calcium threonate. Investigators measured mineralized nodule surface area using computerized image analysis, quantified total and collagenase-digestible protein via radioactive proline and glycine incorporation, and examined collagen and fibronectin co-localization by immunofluorescence.

What was found

Cultures treated with metabolite-supplemented ascorbate demonstrated an increased area of mineralized nodules after 5 weeks and significant increases in total protein synthesis, with collagenous proteins accounting for 85% of that increase. The largest difference between groups occurred in the cell-associated extracellular matrix fraction. Spiking ascorbate with calcium threonate significantly increased mineralized tissue area relative to unsupplemented ascorbate, but the effect was less than that of the complete metabolite-supplemented ascorbate. Absolute numbers for nodule area and protein amounts were not provided in the abstract.

Why it matters

These findings suggest that specific vitamin C metabolites, such as calcium threonate, enhance extracellular matrix synthesis and mineralization in periodontal regenerative cells, pointing to potential adjuncts for bone graft and periodontal healing.

Limits

The study is entirely in vitro, meaning observed cellular mineralization cannot directly establish clinical efficacy or bone regeneration in patients. The abstract does not specify the number of donor subjects from whom the membranes were harvested, nor does it provide exact quantitative measurements, variances, or p-values for mineralized surface areas.

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