Porous Implants Modulate Healing and Induce Shifts in Local Macrophage Polarization in the Foreign Body Reaction

The foreign body reaction (FBR) to implanted materials is of critical importance when medical devices require biological integration and vascularization to support their proper function (e.g., transcutaneous devices, implanted drug delivery systems, tissue replacements, and sensors). One class of materials that improves FBR outcomes is made by sphere-templating, resulting in porous structures with uniform, interconnected 34 μm pores. With these materials we observe reduced fibrosis and increased vascularization. We hypothesized that improved healing is a result of a shift in macrophage polarization, often measured as the ratio of M1 pro-inflammatory cells to M2 pro-healing cells. In this study, macrophage polarity of 34 μm porous implants was compared to non-porous and 160 μm porous implants in subcutaneous mouse tissue. Immunohistochemistry revealed that macrophages in implant pores displayed a shift towards an M1 phenotype compared to externalized cells. Macrophages in 34 μm porous implants had up to 63% greater expression of M1 markers and up to 85% reduction in M2 marker expression (p < 0.05). Macrophages immediately outside the porous structure, in contrast, showed a significant enrichment in M2 phenotypic cells. This study supports a role for macrophage polarization in driving the FBR to implanted materials.

[1]  Ming-Huei Cheng,et al.  The role of pore size on vascularization and tissue remodeling in PEG hydrogels. , 2011, Biomaterials.

[2]  Il Keun Kwon,et al.  Proteomic analysis and quantification of cytokines and chemokines from biomaterial surface-adherent macrophages and foreign body giant cells. , 2007, Journal of biomedical materials research. Part A.

[3]  James M. Anderson,et al.  Biological Responses to Materials , 2001 .

[4]  David Julius,et al.  Cellular and Molecular Mechanisms of Pain , 2009, Cell.

[5]  J. Triffitt,et al.  A review on macrophage responses to biomaterials , 2006, Biomedical Materials.

[6]  W Kenneth Ward,et al.  The effect of microgeometry, implant thickness and polyurethane chemistry on the foreign body response to subcutaneous implants. , 2002, Biomaterials.

[7]  J W Eaton,et al.  Natural Responses to Unnatural Materials: A Molecular Mechanism for Foreign Body Reactions , 1999, Molecular medicine.

[8]  M. Harmsen,et al.  Cytokine and chemokine dynamics differ between rats and mice after collagen implantation , 2007, Journal of tissue engineering and regenerative medicine.

[9]  H. van Goor,et al.  Macrophage diversity in renal injury and repair. , 2008, The Journal of clinical investigation.

[10]  J. Tidball,et al.  Regulatory interactions between muscle and the immune system during muscle regeneration. , 2010, American journal of physiology. Regulatory, integrative and comparative physiology.

[11]  M. Bissell Cellular Plasticity of Inflammatory Myeloid Cells in the Peritoneal Foreign Body Response , 2011 .

[12]  A. Hiltner,et al.  Role for interleukin-4 in foreign-body giant cell formation on a poly(etherurethane urea) in vivo. , 1995, Journal of biomedical materials research.

[13]  M. Textor,et al.  Effect of titanium surface topography on macrophage activation and secretion of proinflammatory cytokines and chemokines. , 2004, Journal of biomedical materials research. Part A.

[14]  T. Gotoh,et al.  Shifts in macrophage phenotypes and macrophage competition for arginine metabolism affect the severity of muscle pathology in muscular dystrophy. , 2008, Human molecular genetics.

[15]  J. Santerre,et al.  Effect of polyurethane chemistry and protein coating on monocyte differentiation towards a wound healing phenotype macrophage. , 2009, Biomaterials.

[16]  Peter Thomsen,et al.  The inflammatory cell influx and cytokines changes during transition from acute inflammation to fibrous repair around implanted materials , 2006, Journal of biomaterials science. Polymer edition.

[17]  R. Bellamkonda,et al.  Effect of modulating macrophage phenotype on peripheral nerve repair. , 2012, Biomaterials.

[18]  Uwe Klinge,et al.  The lightweight and large porous mesh concept for hernia repair , 2005, Expert review of medical devices.

[19]  James M. Anderson,et al.  Quantitative in vivo cytokine analysis at synthetic biomaterial implant sites. , 2008, Journal of biomedical materials research. Part A.

[20]  Alberto Mantovani,et al.  Tumour-associated macrophages are a distinct M2 polarised population promoting tumour progression: potential targets of anti-cancer therapy. , 2006, European journal of cancer.

[21]  P. McLaughlin,et al.  Effect of biomaterial surface charge on the inflammatory response: evaluation of cellular infiltration and TNF alpha production. , 1996, Journal of biomedical materials research.

[22]  W. Kao,et al.  In vivo modulation of host response and macrophage behavior by polymer networks grafted with fibronectin-derived biomimetic oligopeptides: the role of RGD and PHSRN domains. , 2001, Biomaterials.

[23]  Silvano Sozzani,et al.  The chemokine system in diverse forms of macrophage activation and polarization. , 2004, Trends in immunology.

[24]  A. F. Recum,et al.  The influence of micro-topography on cellular response and the implications for silicone implants , 1996 .

[25]  A. Dunne,et al.  The Interleukin-1 Receptor/Toll-Like Receptor Superfamily: Signal Transduction During Inflammation and Host Defense , 2000, Science's STKE.

[26]  S. Badylak,et al.  Macrophage phenotype as a determinant of biologic scaffold remodeling. , 2008, Tissue engineering. Part A.

[27]  George P McCabe,et al.  Macrophage phenotype and remodeling outcomes in response to biologic scaffolds with and without a cellular component. , 2009, Biomaterials.

[28]  Patrick M Flood,et al.  The role of titanium surface topography on J774A.1 macrophage inflammatory cytokines and nitric oxide production. , 2006, Biomaterials.

[29]  D. Mosser,et al.  The many faces of macrophage activation , 2003, Journal of leukocyte biology.

[30]  C. Nathan,et al.  Nitric oxide and macrophage function. , 1997, Annual review of immunology.

[31]  Buddy D. Ratner,et al.  A paradigm shift: biomaterials that heal , 2007 .

[32]  P. Tengvall,et al.  In vivo cell recruitment, cytokine release and chemiluminescence response at gold, and thiol functionalized surfaces. , 1999, Biomaterials.

[33]  T. V. van Kooten,et al.  The influence of micro-topography on cellular response and the implications for silicone implants. , 1995, Journal of Biomaterials Science. Polymer Edition.

[34]  W M Reichert,et al.  Engineering the tissue which encapsulates subcutaneous implants. III. Effective tissue response times. , 1998, Journal of biomedical materials research.

[35]  Lauran R. Madden,et al.  Proangiogenic scaffolds as functional templates for cardiac tissue engineering , 2010, Proceedings of the National Academy of Sciences.

[36]  S Gordon,et al.  Interleukin 4 potently enhances murine macrophage mannose receptor activity: a marker of alternative immunologic macrophage activation , 1992, The Journal of experimental medicine.

[37]  James M. Anderson,et al.  Foreign body reaction to biomaterials. , 2008, Seminars in immunology.

[38]  Julie H. Campbell,et al.  Gene expression profile of the fibrotic response in the peritoneal cavity. , 2010, Differentiation; research in biological diversity.

[39]  Jessica K. Alexander,et al.  Identification of Two Distinct Macrophage Subsets with Divergent Effects Causing either Neurotoxicity or Regeneration in the Injured Mouse Spinal Cord , 2009, The Journal of Neuroscience.

[40]  R. C. Johnson,et al.  Neovascularization of synthetic membranes directed by membrane microarchitecture. , 1995, Journal of biomedical materials research.

[41]  Alberto Mantovani,et al.  Transcriptional Profiling of the Human Monocyte-to-Macrophage Differentiation and Polarization: New Molecules and Patterns of Gene Expression1 , 2006, The Journal of Immunology.

[42]  I Rovira,et al.  Nitric oxide , 2021, Reactions Weekly.

[43]  Jacqueline A. Jones,et al.  Phenotypic dichotomies in the foreign body reaction. , 2007, Biomaterials.

[44]  T. Wynn,et al.  Cellular and molecular mechanisms of fibrosis , 2008, The Journal of pathology.

[45]  S. Forbes,et al.  Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair. , 2005, The Journal of clinical investigation.

[46]  H. Anders,et al.  Renal microenvironments and macrophage phenotypes determine progression or resolution of renal inflammation and fibrosis. , 2011, Kidney international.

[47]  Helen H. Hobbs,et al.  Identification of Scavenger Receptor SR-BI as a High Density Lipoprotein Receptor , 1996, Science.

[48]  T. Wynn,et al.  Obstacles and opportunities for understanding macrophage polarization , 2011, Journal of leukocyte biology.

[49]  Takehisa Matsuda,et al.  In vivo leukocyte cytokine mRNA responses to biomaterials are dependent on surface chemistry. , 2003, Journal of biomedical materials research. Part A.

[50]  G. Zlabinger,et al.  Human adipose tissue macrophages are of an anti-inflammatory phenotype but capable of excessive pro-inflammatory mediator production , 2007, International Journal of Obesity.

[51]  J. Stenken,et al.  Multiplexed cytokine detection of interstitial fluid collected from polymeric hollow tube implants--a feasibility study. , 2008, Cytokine.

[52]  J M Anderson,et al.  Protein-mediated macrophage adhesion and activation on biomaterials: a model for modulating cell behavior , 1999, Journal of materials science. Materials in medicine.

[53]  I. Charles,et al.  Nitric oxide synthase is expressed in human macrophages during foreign body inflammation. , 1997, The American journal of pathology.

[54]  Yan Shi,et al.  Inflammasome components Asc and caspase-1 mediate biomaterial-induced inflammation and foreign body response , 2011, Proceedings of the National Academy of Sciences.

[55]  M. Harmsen,et al.  Cellular and molecular dynamics in the foreign body reaction. , 2006, Tissue engineering.

[56]  I. Nolte,et al.  A comparison of different nanostructured biomaterials in subcutaneous tissue , 2008, Journal of materials science. Materials in medicine.

[57]  C. Isacke,et al.  The mannose receptor family. , 2002, Biochimica et biophysica acta.

[58]  Bruce Klitzman,et al.  In vivo cytokine-associated responses to biomaterials. , 2009, Biomaterials.