Human bone cell cultures in biocompatibility testing. Part II: effect of ascorbic acid, β-glycerophosphate and dexamethasone on osteoblastic differentiation

This work analyses the proliferation/differentiation behaviour of human bone marrow cells cultured in α-minimum essential medium supplemented with 10% foetal bovine serum (standard medium) and in the presence of ascorbic acid (AA, 50 μg ml −1), β-glycerophosphate ( βGP, 10 mmol) and dexamethasone (D...

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Veröffentlicht in:Biomaterials 2000-06, Vol.21 (11), p.1095-1102
Hauptverfasser: Coelho, M.J, Fernandes, M.H
Format: Artikel
Sprache:eng
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Zusammenfassung:This work analyses the proliferation/differentiation behaviour of human bone marrow cells cultured in α-minimum essential medium supplemented with 10% foetal bovine serum (standard medium) and in the presence of ascorbic acid (AA, 50 μg ml −1), β-glycerophosphate ( βGP, 10 mmol) and dexamethasone (Dex, 10 nmol) under selected experimental conditions. Cultures were compared concerning cell morphology, cell growth, ALP activity and ability to form calcium phosphate deposits. Cells growing in the various experimental conditions proliferated gradually with the incubation time and presented high ALP activity. Cultures grown in standard medium and in the presence of either AA or Dex failed to form calcium phosphate deposits. Cultures grown in the presence of βGP, βGP+AA and βGP+AA+Dex, i.e. in the presence of a source of phosphate ions, showed the formation of a mineralised extracellular matrix. The presence of Dex resulted in a significant induction in the ALP activity and ability to form mineral deposits. The behaviour of the various cell cultures is in agreement with previous studies stating a reciprocal and functionally coupled relationship between proliferation and differentiation, i.e. cultures grown in a medium containing βGP presented a less proliferative but more differentiated osteoblastic cell population, as compared to cultures lacking the mineralisation process.
ISSN:0142-9612
1878-5905
DOI:10.1016/S0142-9612(99)00192-1