Tasaki Akira, Yamanaka Naoki, Kubo Makoto, Matsumoto Kotaro, Kuroki Hideo, Nakamura Katsuya, Nakahara Chihiro, Onishi Hideya, Kuga Hirotaka, Baba Eishi, Tanaka Masao, Morisaki Takashi, Katano Mitsuo
Department of Cancer Therapy and Research, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8525, Japan.
J Immunol Methods. 2004 Apr;287(1-2):79-90. doi: 10.1016/j.jim.2004.01.014.
Dendritic cell-like cells (Mo-DCs) generated from peripheral blood monocytes with interleukin-4 (IL-4) and granulocyte-macrophage colony-stimulating factor (GM-CSF) have been used as tools to treat cancer patients (DC-vaccines). Because Mo-DCs have multiple antigen presentation-related functions, including phagocytosis, migration, cytokine production, and T cell stimulation, establishment of a method for simultaneously evaluating the various functions of Mo-DCs is important. We developed a new in vitro three-dimensional two-layer collagen matrix culture model that consists of a collagen gel containing Mo-DCs as the lower layer and a collagen gel containing necrotic GCTM-1 tumor cells and/or T cells as the upper layer. We used this system to observe simultaneously multiple functions of Mo-DCs by phase-contrast or fluorescence microscopy and to assess IL-12 secretion during more than 2 weeks of culture. We also observed interactions between Mo-DCs and necrotic GCTM-1 or T cells on an individual cell basis by time-lapse videomicroscopy. In addition, we collected Mo-DCs from the collagen gels by collagenase treatment and analyzed the expression of antigen presentation-related molecules such as HLA-DR, CD80, CD83, and CD86 on Mo-DCs. This model may be a useful tool for evaluation of the various functions of Mo-DCs used as DC vaccines and for studies of the complex behaviors of Mo-DCs in vivo.
由外周血单核细胞与白细胞介素-4(IL-4)和粒细胞巨噬细胞集落刺激因子(GM-CSF)生成的树突状细胞样细胞(Mo-DC)已被用作治疗癌症患者的工具(DC疫苗)。由于Mo-DC具有多种与抗原呈递相关的功能,包括吞噬作用、迁移、细胞因子产生和T细胞刺激,因此建立一种同时评估Mo-DC各种功能的方法很重要。我们开发了一种新的体外三维双层胶原基质培养模型,该模型由含有Mo-DC的胶原凝胶作为下层和含有坏死GCTM-1肿瘤细胞和/或T细胞的胶原凝胶作为上层组成。我们使用该系统通过相差显微镜或荧光显微镜同时观察Mo-DC的多种功能,并评估培养超过2周期间的IL-12分泌。我们还通过延时视频显微镜在单个细胞水平上观察Mo-DC与坏死GCTM-1或T细胞之间的相互作用。此外,我们通过胶原酶处理从胶原凝胶中收集Mo-DC,并分析Mo-DC上抗原呈递相关分子如HLA-DR、CD80、CD83和CD86的表达。该模型可能是评估用作DC疫苗的Mo-DC各种功能以及研究Mo-DC在体内复杂行为的有用工具。