| Literature DB >> 25982003 |
Werner E G Müller1, Emad Tolba2,3, Heinz C Schröder2, Xiaohong Wang4.
Abstract
The initial mineralization centers during human bone formation onto osteoblasts are composed of CaCO3 . Those bioseeds are enzymatically formed via carbonic anhydrase(s) in close association with the cell surface of the osteoblasts. Subsequently, the bicarbonate/carbonate anions are exchanged non-enzymatically by inorganic phosphate [Pi ]. One source for the supply of Pi is polyphosphate [polyP] which is a physiological polymer, formed in the osteoblasts as well as in the platelets. The energy-rich acid anhydride bonds within the polyP chain are cleaved by phosphatase(s); during this reaction free-energy might be released that could be re-used, as metabolic fuel, for the maintenance of the steady-state concentrations of the substrates/products during mineralization. Finally it is outlined that polyP, as a morphogenetically active scaffold, is even suitable for 3D cell printing.Entities:
Keywords: bone; morphogenetic activity; polyphosphate; regenerative medicine; tissue engineering
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Year: 2015 PMID: 25982003 DOI: 10.1002/mabi.201500100
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979