Gupta L C, Singla S K, Tandon C, Jethi R K
Department of Biochemistry, Panjab University, Chandigarh-1 60014, India.
Magnes Res. 2004 Jun;17(2):67-71.
At physiological concentrations, Mg2+ has been found to be a potent inhibitor of collagen-induced in vitro mineralization. Mg2+ inhibits mineralization by competing with Ca2+ for specific phosphate independent Ca2+ binding sites of the catalytic matrix. Matrix bound Mg2+ subsequently reacts with HPO4(2-) to form MgHPO4 complex which can not be further converted to the matrix bound mineral phase. The matrix, as well as the mineral phase associated with the matrix, influence the rate of mineralization.
在生理浓度下,已发现Mg2+是胶原诱导的体外矿化的有效抑制剂。Mg2+通过与Ca2+竞争催化基质中特定的非磷酸依赖性Ca2+结合位点来抑制矿化。与基质结合的Mg2+随后与HPO4(2-)反应形成MgHPO4复合物,该复合物不能进一步转化为与基质结合的矿化相。基质以及与基质相关的矿化相都会影响矿化速率。