Martowicz Agnieszka, Kern Johann, Gunsilius Eberhard, Untergasser Gerold
Department of Internal Medicine V, Innsbruck Medical University; Division of Vascular Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institute.
Department of Internal Medicine V, Innsbruck Medical University; Oncotyrol GmbH.
J Vis Exp. 2015 May 1(99):e52665. doi: 10.3791/52665.
Multiple myeloma (MM), a malignant plasma cell disease, remains incurable and novel drugs are required to improve the prognosis of patients. Due to the lack of the bone microenvironment and auto/paracrine growth factors human MM cells are difficult to cultivate. Therefore, there is an urgent need to establish proper in vitro and in vivo culture systems to study the action of novel therapeutics on human MM cells. Here we present a model to grow human multiple myeloma cells in a complex 3D environment in vitro and in vivo. MM cell lines OPM-2 and RPMI-8226 were transfected to express the transgene GFP and were cultivated in the presence of human mesenchymal cells and collagen type-I matrix as three-dimensional spheroids. In addition, spheroids were grafted on the chorioallantoic membrane (CAM) of chicken embryos and tumor growth was monitored by stereo fluorescence microscopy. Both models allow the study of novel therapeutic drugs in a complex 3D environment and the quantification of the tumor cell mass after homogenization of grafts in a transgene-specific GFP-ELISA. Moreover, angiogenic responses of the host and invasion of tumor cells into the subjacent host tissue can be monitored daily by a stereo microscope and analyzed by immunohistochemical staining against human tumor cells (Ki-67, CD138, Vimentin) or host mural cells covering blood vessels (desmin/ASMA). In conclusion, the onplant system allows studying MM cell growth and angiogenesis in a complex 3D environment and enables screening for novel therapeutic compounds targeting survival and proliferation of MM cells.
多发性骨髓瘤(MM)是一种恶性浆细胞疾病,目前仍无法治愈,因此需要新型药物来改善患者的预后。由于缺乏骨微环境以及自身/旁分泌生长因子,人类MM细胞难以培养。因此,迫切需要建立合适的体外和体内培养系统,以研究新型治疗方法对人类MM细胞的作用。在此,我们展示了一种在体外和体内的复杂三维环境中培养人类多发性骨髓瘤细胞的模型。将MM细胞系OPM-2和RPMI-8226转染以表达转基因绿色荧光蛋白(GFP),并在人骨髓间充质细胞和I型胶原基质存在的情况下培养成三维球体。此外,将球体移植到鸡胚的绒毛尿囊膜(CAM)上,并通过立体荧光显微镜监测肿瘤生长。这两种模型都可以在复杂的三维环境中研究新型治疗药物,并通过转基因特异性GFP-ELISA对移植瘤匀浆后的肿瘤细胞数量进行定量。此外,每天可以通过立体显微镜监测宿主的血管生成反应以及肿瘤细胞向下方宿主组织的侵袭情况,并通过针对人类肿瘤细胞(Ki-67、CD138、波形蛋白)或覆盖血管的宿主壁细胞(结蛋白/平滑肌肌动蛋白)的免疫组织化学染色进行分析。总之,该移植系统能够在复杂的三维环境中研究MM细胞的生长和血管生成,并能够筛选针对MM细胞存活和增殖的新型治疗化合物。