4.6 Article

Proteomic Analysis of Mesenchymal Stem Cells and Monocyte Co-Cultures Exposed to a Bioactive Silica-Based Sol-Gel Coating

Journal

ACS BIOMATERIALS SCIENCE & ENGINEERING
Volume 9, Issue 6, Pages 3306-3319

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.3c00254

Keywords

biomaterials; osteoimmunology; co-cultures; proteomics; sol-gel coatings

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New methodologies, such as proteomics, are necessary to improve in vitro characterization methods and better model natural tissues by analyzing cell-material interactions. In this study, label-free liquid chromatography tandem mass spectrometry proteomic methods were used to characterize the effects of a bioactive sol-gel coating on co-cultured human mesenchymal stem cells (MSCs) and CD14(+) monocytes. The results showed that the material mainly affected cell adhesion, while both cellular cross-talk and the material impacted inflammation.
New methodologiescapable of extensively analyzing thecell-materialinteractions are necessary to improve current in vitro characterizationmethods, and proteomics is a viable alternative. Also, many studiesare focused on monocultures, even though co-cultures model betterthe natural tissue. For instance, human mesenchymal stem cells (MSCs)modulate immune responses and promote bone repair through interactionwith other cell types. Here, label-free liquid chromatography tandemmass spectroscopy proteomic methods were applied for the first timeto characterize HUCPV (MSC) and CD14(+) monocytes co-culturesexposed to a bioactive sol-gel coating (MT). PANTHER, DAVID,and STRING were employed for data integration. Fluorescence microscopy,enzyme-linked immunosorbent assay, and ALP activity were measuredfor further characterization. Regarding the HUCPV response, MT mainlyaffected cell adhesion by decreasing integrins, RHOC, and CAD13 expression.In contrast, MT augmented CD14(+) cell areas and integrins,Rho family GTPases, actins, myosins, and 14-3-3 expression. Also,anti-inflammatory (APOE, LEG9, LEG3, and LEG1) and antioxidant (peroxiredoxins,GSTO1, GPX1, GSHR, CATA, and SODM) proteins were overexpressed. Onco-cultures, collagens (CO5A1, CO3A1, CO6A1, CO6A2, CO1A2, CO1A1,and CO6A3), cell adhesion, and pro-inflammatory proteins were downregulated.Thus, cell adhesion appears to be mainly regulated by the material,while inflammation is impacted by both cellular cross-talk and thematerial. Altogether, we conclude that applied proteomic approachesshow its potential in biomaterial characterization, even in complexsystems.

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