Müller Werner E G, Tolba Emad, Schröder Heinz C, Wang Xiaohong
ERC Advanced Investigator Grant Research Group at the Institute for Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, Duesbergweg 6, D-55128 Mainz, Germany.
Biomaterials Department, Inorganic Chemical Industries Division, National Research Center, Doki Cairo, 11884, Egypt.
Macromol Biosci. 2015 Sep;15(9):1182-97. doi: 10.1002/mabi.201500100. Epub 2015 May 15.
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.
人类骨形成过程中在成骨细胞上的初始矿化中心由碳酸钙组成。这些生物种子通过碳酸酐酶与成骨细胞的细胞表面紧密结合而酶促形成。随后,碳酸氢根/碳酸根阴离子通过无机磷酸盐[Pi]进行非酶交换。Pi的一个来源是多聚磷酸盐[polyP],它是一种生理聚合物,在成骨细胞和血小板中形成。多聚P链内富含能量的酸酐键被磷酸酶裂解;在此反应过程中可能会释放自由能,该自由能可作为代谢燃料被重新利用,以维持矿化过程中底物/产物的稳态浓度。最后概述了多聚P作为一种具有形态发生活性的支架,甚至适用于3D细胞打印。