The proposed studies continue to address the hypotheses that the monocyte/macrophage is the major cellular component controlling the tissue/material inflammatory, foreign body, and wound healing responses, and that monocyte, macrophage, and foreign body giant cell (FBGC) adhesion receptor/biomaterial surface interactions and cytokine production are differentially affected by material surface properties. In the present application, our objectives have been significantly expanded to encompass the influences of biomaterial surface chemistries or inflammatory monocyte/macrophage recruitment, chemokine and matrix proteinase production, matrix deposition mechanisms of apoptosis, and the responses of wound healing cells. Therefore, the specific aims of this project have been designed to address the effects of material surface chemistry on major biological response mechanism, that represent multiple and interrelated aspects of the foreign body reaction.
The specific aims of the project are: 1) To determine the mechanisms of monocyte/macrophage recruitment, activation, and production of chemokines and cytokines; 2) To elucidate the mechanisms of monocyte, macrophage, and FBGC adhesion, matrix production, ant matrix proteolysis; 3) To investigate the mechanisms of monocyte/macrophage-derived chemokine, cytokine, and matrix/matrix proteinase-mediated wound healing responses; and 4) To determine the material-dependent cellular mechanisms by which the presence of adherent macrophages and FBGC can be controlled with apoptosis. Based on the results of our previous studies, four different model surface-modified material systems for inflammatory and wound healing interactions have been selected for this investigation. These material systems provide for a wide range of surface chemistries currently being used in clinical devices and prostheses as well as in the development ot new materials and devices. The model surface-modified systems are: 1) RGD-modified surfaces; 2) photopolymerized graft polymers; 3) silane-modified molecularly engineered surfaces; and 4) temperature responsive surfaces. Correlative in vitro cell culture and in vivo murine cage and subcutaneous implant models will be utilized to address the hypotheses and specific aims with state-of-the-art gene expression array analysis, flow cytometry, fluorescence confocal scanning laser microscopy (FCSLM), cell migration assays, ELISAs, functional inhibition studies, metabolic labeling, immunohistochemical analysis, and apoptosis assessment.
| Chang, David T; Colton, Erica; Anderson, James M (2009) Paracrine and juxtacrine lymphocyte enhancement of adherent macrophage and foreign body giant cell activation. J Biomed Mater Res A 89:490-8 |
| Brodbeck, William G; Anderson, James M (2009) Giant cell formation and function. Curr Opin Hematol 16:53-7 |
| Chang, David T; Colton, Erica; Matsuda, Takehisa et al. (2009) Lymphocyte adhesion and interactions with biomaterial adherent macrophages and foreign body giant cells. J Biomed Mater Res A 91:1210-20 |
| Anderson, James M; Rodriguez, Analiz; Chang, David T (2008) Foreign body reaction to biomaterials. Semin Immunol 20:86-100 |
| Chang, David T; Jones, Jacqueline A; Meyerson, Howard et al. (2008) Lymphocyte/macrophage interactions: biomaterial surface-dependent cytokine, chemokine, and matrix protein production. J Biomed Mater Res A 87:676-87 |
| Fujii, Yasuo; Anderson, James M; Matsuda, Takehisa (2008) Antibody-bound cell microarray for immunophenotyping: surface modification and lymphocyte subpopulations. J Biomed Mater Res B Appl Biomater 87:525-37 |
| Jones, Jacqueline A; Qin, L Abby; Meyerson, Howard et al. (2008) Instability of self-assembled monolayers as a model material system for macrophage/FBGC cellular behavior. J Biomed Mater Res A 86:261-8 |
| Jones, Jacqueline A; McNally, Amy K; Chang, David T et al. (2008) Matrix metalloproteinases and their inhibitors in the foreign body reaction on biomaterials. J Biomed Mater Res A 84:158-66 |
| McNally, Amy K; Macewan, Sarah R; Anderson, James M (2008) Foreign body-type multinucleated giant cell formation requires protein kinase C beta, delta, and zeta. Exp Mol Pathol 84:37-45 |
| McNally, Amy K; Jones, Jacqueline A; Macewan, Sarah R et al. (2008) Vitronectin is a critical protein adhesion substrate for IL-4-induced foreign body giant cell formation. J Biomed Mater Res A 86:535-43 |
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