Abstract

Biomineralization is the process by which organisms produce hard inorganic matter from soft tissues with outstanding control of mineral deposition in time and space. For this purpose, organisms deploy a sophisticated “toolkit” that has resulted in significant evolutionary innovations, for which calcium phosphate (CaP) is the biomineral selected for the skeleton of vertebrates. While CaP mineral formation in aqueous media can be investigated by studying thermodynamics and kinetics of phase transitions in supersaturated solutions, biogenic mineralization requires coping with the inherent complexity of biological systems. This mainly includes compartmentalization and homeostatic processes used by organisms to regulate key physiological factors, including temperature, pH and ion concentration. A detailed analysis of the literature shows the emergence of two main views describing the mechanism of CaP biomineralization. The first one, more dedicated to the study of in vivo systems and supported by researchers in physiology, often involves matrix vesicles (MVs). The second one, more investigated by the physicochemistry community, involves collagen intrafibrillar mineralization particularly through in vitro acellular models. Herein, we show that there is an obvious need in the biological systems to control both where and when the mineral forms through an in-depth survey of the mechanism of CaP mineralization. This necessity could gather both communities of physiologists and physicochemists under a common interest for an enzymatic approach to better describe CaP biomineralization. Both homogeneous and heterogeneous enzymatic catalyses are conceivable for these systems, and a few preliminary promising results on CaP mineralization for both types of enzymatic catalysis are reported in this work. Through them, we aim to describe the relevance of our point of view and the likely findings that could be obtained when adding an enzymatic approach to the already rich and creative research field dealing with CaP mineralization. This complementary approach could lead to a better understanding of the biomineralization mechanism and inspire the biomimetic design of new materials.

Highlights

  • This paper aims to point out particular aspects, either experimental or conceptual, that are of primary importance to understanding the chemical and biochemical processes involved in calcium phosphate (CaP) biomineralization

  • We show the benefits of using an enzymatic approach to investigate the mechanism of CaP mineralization. Considering these aspects is essential to making progress in reconciling disparate physicochemical and physiological views with the aim to decipher the mechanism of CaP biomineralization

  • Via matrix vesicles (MVs) or intracellular CaP and within collagen fibrils, could, in harmony, explain the formation of the outstanding hybrid systems described above, these pathways need to accurately coincide in order to ensure the complete mineralization of the extracellular matrix (ECM) and yield these complex hybrid architectures

Read more

Summary

A Contribution to Reconcile the Physicochemical with the Physiological View

Citation: Guibert, C.; Landoulsi, J. Contribution to Reconcile the Physicochemical with the Physiological View. Int. J. Mol. Sci. Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in Sorbonne Université, CNRS, Laboratoire de Réactivité de Surface, LRS, F-75005 Paris, France Université de Technologie de Compiègne, CNRS, Laboratoire de Biomécanique & Bioingénierie, F-60205 Compiègne, France

Introduction
CaP Mineralization Process
Factors Influencing CaP Nucleation and Growth
Biogenic Mineralization
Collagen Fibrils
Intrafibrillar Mechanisms
Matrix Vesicles
Enzymatic Approach
Alkaline Phosphatase
Homogeneous Catalysis
Heterogeneous Catalysis
Findings
Confinement
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call