Lymphocyte adhesion and interactions with biomaterial adherent macrophages and foreign body giant cells

• Published in: Journal of biomedical materials research. Part A Vol. 91A; no. 4; pp. 1210 - 1220
• Main Authors: Chang, David T., Colton, Erica, Matsuda, Takehisa, Anderson, James M.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.12.2009
• Subjects: Activation; Adhesion; Biocompatible Materials - pharmacology; Biomaterials; Biomedical materials; Cell Adhesion - drug effects; Cell Communication - drug effects; cytokines; Fluorescent Antibody Technique; Giant Cells, Foreign-Body - cytology; Giant Cells, Foreign-Body - drug effects; Giant Cells, Foreign-Body - metabolism; Humans; lymphocyte activation; Lymphocyte Count; Lymphocyte Subsets - cytology; Lymphocyte Subsets - drug effects; Lymphocyte Subsets - metabolism; Lymphocytes; Lymphocytes - cytology; Lymphocytes - drug effects; Lymphocytes - metabolism; Lymphokines - biosynthesis; Macrophages; Macrophages - cytology; Macrophages - drug effects; Macrophages - metabolism; macrophages and foreign body giant cells; Surface chemistry; Surface Properties - drug effects; Surgical implants
• ISSN: 1549-3296; 1552-4965; 1552-4965
• DOI: 10.1002/jbm.a.32218

To characterize the effects of adherent macrophages and biomaterial surface chemistries on lymphocyte adhesion and activation, lymphocytes were co‐cultured with monocytes alone and together, directly and separated by a porous membrane transwell on hydrophobic, hydrophilic/neutral, hydrophilic/anionic, and hydrophilic/cationic biomaterial surfaces. Surface adherent cells were quantitatively analyzed after 3 days utilizing immunofluorescence and phase contrast imaging. After periods of 3, 7, and 10 days, secreted interferon‐γ (IFN‐γ) was quantified by ELISA. Limited direct biomaterial‐adherent lymphocytes were identified regardless of the presence of macrophages or foreign body giant cells (FBGC). The majority of adherent lymphocytes, which were T cells (>95%) rather than natural killer cells, predominantly interacted with adherent macrophages and FBGCs; greater than 90% were interacting on surfaces with higher levels of adherent macrophages and FBGCs and greater than 55% were interacting on surfaces with lower levels of macrophages and FBGCs. The hydrophilic/anionic surface promoted higher levels of macrophage‐ and FBGC‐adherent lymphocytes but was nonselective for lymphocyte subtype interactions. The hydrophilic/neutral surface was selective for CD4+ T lymphocyte interactions while the hydrophobic surface was selective for CD8+ T lymphocyte interactions. IFN‐γ was produced in direct and indirect co‐cultures but not in lymphocyte‐ and monocyte‐only cultures suggesting that lymphocytes are activated via macrophage‐derived cytokines rather than direct biomaterial contact. Direct lymphocyte interactions with adherent macrophages/FBGCs enhanced IFN‐γ production relative to indirect co‐cultures. These results suggest that lymphocytes prefer interactions with adherent macrophages and FBGCs, resulting in lymphocyte activation, and these interactions can be influenced by biomaterial surface chemistries. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2009