Department of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio 44106, USA.
J Biomed Mater Res A. 2009 Dec 15;91(4):1210-20. 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-gamma (IFN-gamma) 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-gamma 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-gamma 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.
为了研究贴壁巨噬细胞和生物材料表面化学性质对淋巴细胞黏附和激活的影响,我们将淋巴细胞与单核细胞单独和共同共培养,直接共培养以及通过多孔膜 Transwell 间接共培养,共培养的生物材料表面包括疏水性、亲水性/中性、亲水性/阴离子性和亲水性/阳离子性表面。3 天后,利用免疫荧光和相差成像对贴壁细胞进行定量分析。培养 3、7 和 10 天后,通过 ELISA 定量检测分泌的干扰素-γ(IFN-γ)。无论是否存在巨噬细胞或异物巨细胞(FBGC),都只能检测到有限的直接黏附于生物材料的淋巴细胞。大多数黏附的淋巴细胞(>95%为 T 细胞而非自然杀伤细胞)主要与贴壁巨噬细胞和 FBGC 相互作用;>90%的相互作用发生在黏附巨噬细胞和 FBGC 水平较高的表面上,>55%的相互作用发生在黏附巨噬细胞和 FBGC 水平较低的表面上。亲水性/阴离子性表面促进了更多的巨噬细胞和 FBGC 黏附的淋巴细胞,但对淋巴细胞亚型的相互作用没有选择性。亲水性/中性表面对 CD4+T 淋巴细胞的相互作用具有选择性,而疏水性表面对 CD8+T 淋巴细胞的相互作用具有选择性。IFN-γ在直接和间接共培养物中产生,但在仅淋巴细胞和单核细胞的培养物中不产生,这表明淋巴细胞是通过巨噬细胞衍生的细胞因子而不是直接与生物材料接触而被激活的。与间接共培养物相比,直接与黏附的巨噬细胞/FBGC 相互作用增强了 IFN-γ的产生。这些结果表明,淋巴细胞更喜欢与黏附的巨噬细胞和 FBGC 相互作用,导致淋巴细胞激活,并且这些相互作用可以受到生物材料表面化学性质的影响。