Osteogenic Cell Cultures Cannot Utilize Exogenous Sources of Synthetic Polyphosphate for Mineralization. Issue 12 (15th October 2014)
- Record Type:
- Journal Article
- Title:
- Osteogenic Cell Cultures Cannot Utilize Exogenous Sources of Synthetic Polyphosphate for Mineralization. Issue 12 (15th October 2014)
- Main Title:
- Osteogenic Cell Cultures Cannot Utilize Exogenous Sources of Synthetic Polyphosphate for Mineralization
- Authors:
- Ariganello, Marianne B.
Omelon, Sidney
Variola, Fabio
Wazen, Rima M.
Moffatt, Pierre
Nanci, Antonio - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jcb24886-sec-0001" sec-type="section"> <p>Phosphate is critical for mineralization and deficiencies in the regulation of free phosphate lead to disease. Inorganic polyphosphates (polyPs) may represent a physiological source of phosphate because they can be hydrolyzed by biological phosphatases. To investigate whether exogenous polyP could be utilized for mineral formation, mineralization was evaluated in two osteogenic cell lines, Saos‐2 and MC3T3, expressing different levels of tissue non‐specific alkaline phosphatase (tnALP). The role of tnALP was further explored by lentiviral‐mediated overexpression in MC3T3 cells. When cells were cultured in the presence of three different phosphate sources, there was a strong mineralization response with β‐glycerophosphate (βGP) and orthophosphate (Pi) but none of the cultures sustained mineralization in the presence of polyP (neither chain length 17‐Pi nor 42‐Pi). Even in the presence of mineralizing levels of phosphate, low concentrations of polyP (50 μM) were sufficient to inhibit mineral formation. Energy‐dispersive X‐ray spectroscopy confirmed the presence of apatite‐like mineral deposits in MC3T3 cultures supplemented with βGP, but not in those with polyP. While von Kossa staining was consistent with the presence or absence of mineral, an unusual Alizarin staining was obtained in polyP‐treated MC3T3 cultures. This staining pattern combined with low<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jcb24886-sec-0001" sec-type="section"> <p>Phosphate is critical for mineralization and deficiencies in the regulation of free phosphate lead to disease. Inorganic polyphosphates (polyPs) may represent a physiological source of phosphate because they can be hydrolyzed by biological phosphatases. To investigate whether exogenous polyP could be utilized for mineral formation, mineralization was evaluated in two osteogenic cell lines, Saos‐2 and MC3T3, expressing different levels of tissue non‐specific alkaline phosphatase (tnALP). The role of tnALP was further explored by lentiviral‐mediated overexpression in MC3T3 cells. When cells were cultured in the presence of three different phosphate sources, there was a strong mineralization response with β‐glycerophosphate (βGP) and orthophosphate (Pi) but none of the cultures sustained mineralization in the presence of polyP (neither chain length 17‐Pi nor 42‐Pi). Even in the presence of mineralizing levels of phosphate, low concentrations of polyP (50 μM) were sufficient to inhibit mineral formation. Energy‐dispersive X‐ray spectroscopy confirmed the presence of apatite‐like mineral deposits in MC3T3 cultures supplemented with βGP, but not in those with polyP. While von Kossa staining was consistent with the presence or absence of mineral, an unusual Alizarin staining was obtained in polyP‐treated MC3T3 cultures. This staining pattern combined with low Ca:P ratios suggests the persistence of Ca‐polyP complexes, even with high residual ALP activity. In conclusion, under standard culture conditions, exogenous polyP does not promote mineral deposition. This is not due to a lack of active ALP, and unless conditions that favor significant processing of polyP are achieved, its mineral inhibitory capacity predominates. J. Cell. Biochem. 115: 2089–2102, 2014. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of cellular biochemistry. Volume 115:Issue 12(2014:Dec.)
- Journal:
- Journal of cellular biochemistry
- Issue:
- Volume 115:Issue 12(2014:Dec.)
- Issue Display:
- Volume 115, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 115
- Issue:
- 12
- Issue Sort Value:
- 2014-0115-0012-0000
- Page Start:
- 2089
- Page End:
- 2102
- Publication Date:
- 2014-10-15
- Subjects:
- Cytochemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4644 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcb.24886 ↗
- Languages:
- English
- ISSNs:
- 0730-2312
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.010000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4273.xml