Influence of biodegradable and non-biodegradable material surfaces on the differentiation of human monocyte-derived macrophages
- PMID: 17924965
- DOI: 10.1111/j.1432-0436.2007.00221.x
Influence of biodegradable and non-biodegradable material surfaces on the differentiation of human monocyte-derived macrophages
Abstract
Monocyte-derived macrophages (MDM) and multinucleated foreign body giant cells (FBGC) are the primary cell types that remain at the cell-material interface of polyurethane (PU)-based medical devices as a result of chronic inflammatory responses. In vitro studies have demonstrated that MDM possess degradative potential toward PU, which can result in device failure. Because most studies have followed the degradation potential, morphology, and function of these cells only once fully differentiated, the current study investigated the influence of a non-degradable control tissue culture-grade polystyrene (TCPS) surface relative to two degradable model polycarbonate-urethanes (PCNU), of different chemistry, on various parameters of MDM morphology and function during a 14-day differentiation time course. The differentiation of human monocytes isolated from whole blood on PCNU materials resulted in increased cell attachment, decreased multinucleation, and significant decreases in cell spreading when compared with cells differentiated on TCPS. Actin-stained podosome-like cell adhesion structures were increased in PCNU-adherent cells, accompanied by an alteration in beta-actin and vinculin protein expression. The expression of the CD68 macrophage marker was reduced when cells were adherent to the PCNU materials and compared with TCPS, suggesting altered cell activation by the degradable relative to non-degradable materials. The degradative potential of these cells was altered by the material surface they were exposed to as measured by esterase activity and protein expression of monocyte-specific esterase. This was also supported by physical material breakdown evident in scanning electron microscopy images that illustrated holes in the PCNU films generated by the presence of differentiating MDM. It was concluded from these studies that PCNU materials significantly alter the function and morphology of differentiating MDM. This must be taken into consideration when studying cell-material interactions because these cells will receive cues from their immediate environment (including the biomaterial) upon differentiation, thereby affecting their resulting phenotype.
Similar articles
-
Effect of polyurethane chemistry and protein coating on monocyte differentiation towards a wound healing phenotype macrophage.Biomaterials. 2009 Oct;30(29):5497-504. doi: 10.1016/j.biomaterials.2009.07.010. Epub 2009 Jul 26. Biomaterials. 2009. PMID: 19635633
-
The human macrophage response during differentiation and biodegradation on polycarbonate-based polyurethanes: dependence on hard segment chemistry.Biomaterials. 2005 Dec;26(35):7357-66. doi: 10.1016/j.biomaterials.2005.05.048. Biomaterials. 2005. PMID: 16005062
-
Differentiation of monocytes on a degradable, polar, hydrophobic, ionic polyurethane: Two-dimensional films vs. three-dimensional scaffolds.Acta Biomater. 2011 Jan;7(1):115-22. doi: 10.1016/j.actbio.2010.08.014. Epub 2010 Aug 20. Acta Biomater. 2011. PMID: 20728587
-
Synthesis of cholesterol esterase by monocyte-derived macrophages: a potential role in the biodegradation of poly(urethane)s.J Biomater Appl. 1999 Jan;13(3):187-205. doi: 10.1177/088532829901300302. J Biomater Appl. 1999. PMID: 9934625 Review.
-
Macrophages: development and tissue specialization.Annu Rev Immunol. 2015;33:643-75. doi: 10.1146/annurev-immunol-032414-112220. Annu Rev Immunol. 2015. PMID: 25861979 Review.
Cited by
-
Comparison of different cell culture plates for the enrichment of non-adherent human mononuclear cells.Exp Ther Med. 2019 Mar;17(3):2004-2012. doi: 10.3892/etm.2019.7204. Epub 2019 Jan 25. Exp Ther Med. 2019. PMID: 30867690 Free PMC article.
-
Characterization and biocompatibility studies of new degradable poly(urea)urethanes prepared with arginine, glycine or aspartic acid as chain extenders.J Mater Sci Mater Med. 2013 Jul;24(7):1733-44. doi: 10.1007/s10856-013-4931-4. Epub 2013 Apr 25. J Mater Sci Mater Med. 2013. PMID: 23615787
-
Polymer-free corticosteroid dimer implants for controlled and sustained drug delivery.Nat Commun. 2021 May 17;12(1):2875. doi: 10.1038/s41467-021-23232-7. Nat Commun. 2021. PMID: 34001908 Free PMC article.
-
Elastase-sensitive elastomeric scaffolds with variable anisotropy for soft tissue engineering.Pharm Res. 2008 Oct;25(10):2400-12. doi: 10.1007/s11095-008-9628-x. Epub 2008 May 29. Pharm Res. 2008. PMID: 18509596 Free PMC article.
-
Macrophage differentiation and polarization on a decellularized pericardial biomaterial.Biomaterials. 2011 Jan;32(2):439-49. doi: 10.1016/j.biomaterials.2010.09.004. Epub 2010 Oct 12. Biomaterials. 2011. PMID: 20933269 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources