Complex effects of Mg-biomaterials on the osteoblast cell machinery: A proteomic study
Divalent cations
Proteomics
Integrins
0303 health sciences
Osteoblasts
Cell-material interactions
Cell adhesion
cell adhesion
Biocompatible Materials
divalent cations
osteogenesis
Biomaterials
03 medical and health sciences
proteomics
Osteogenesis
Tandem Mass Spectrometry
cell–material interactions
Humans
biomaterials
Chromatography, Liquid
DOI:
10.1016/j.bioadv.2022.212826
Publication Date:
2022-04-26T00:42:15Z
AUTHORS (10)
ABSTRACT
The cell-biomaterial interface is highly complex; thousands of molecules and many processes participate in its formation. Growing demand for improved biomaterials has highlighted the need to understand the structure and functions of this interface. Proteomic methods offer a viable alternative to the traditional in vitro techniques for analyzing such systems. Magnesium is a promoter of cell adhesion and osteogenesis. Here, we used the LC-MS/MS to compare the protein expression profiles of human osteoblasts (HOb) exposed to sol-gel coatings without (MT) and with Mg (MT1.5Mg) for 1, 3, and 7 days. PANTHER, DAVID, and IPA databases were employed for protein identification and data analysis. Confocal microscopy and gene expression analysis were used for further characterization. Exposure to MT1.5Mg increased the HOb cell area and the expression of SP7, RUNX2, IBP3, COL3A1, MXRA8, and FBN1 genes. Proteomic analysis showed that MT1.5Mg affected the early osteoblast maturation (PI3/AKT, mTOR, ERK/MAPK), insulin metabolism, cell adhesion (integrin, FAK, actin cytoskeleton regulation) and oxidative stress pathways. Thus, the effects of Mg on cell adhesion and osteogenesis are rather complex, affecting several pathways rather than single processes. Our analysis also confirms the potential of proteomics in biomaterial characterization, showing a good correlation with in vitro results.
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