Department of Neuroscience and Mahoney Institute for Neurosciences, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Nat Protoc. 2020 Dec;15(12):4000-4033. doi: 10.1038/s41596-020-0402-9. Epub 2020 Nov 9.
Glioblastoma tumors exhibit extensive inter- and intratumoral heterogeneity, which has contributed to the poor outcomes of numerous clinical trials and continues to complicate the development of effective therapeutic strategies. Most in vitro models do not preserve the cellular and mutational diversity of parent tumors and often require a lengthy generation time with variable efficiency. Here, we describe detailed procedures for generating glioblastoma organoids (GBOs) from surgically resected patient tumor tissue using a chemically defined medium without cell dissociation. By preserving cell-cell interactions and minimizing clonal selection, GBOs maintain the cellular heterogeneity of parent tumors. We include details of how to passage and cryopreserve GBOs for continued use, biobanking and long-term recovery. In addition, we describe procedures for investigating patient-specific responses to immunotherapies by co-culturing GBOs with chimeric antigen receptor (CAR) T cells. It takes ~2-4 weeks to generate GBOs and 5-7 d to perform CAR T cell co-culture using this protocol. Competence with human cell culture, tissue processing, immunohistology and microscopy is required for optimal results.
胶质母细胞瘤肿瘤表现出广泛的肿瘤内和肿瘤间异质性,这导致了许多临床试验的不良结果,并继续使有效的治疗策略的发展复杂化。大多数体外模型不能保留亲本肿瘤的细胞和突变多样性,并且通常需要具有可变效率的较长的生成时间。在这里,我们描述了使用无细胞解离的化学定义培养基从手术切除的患者肿瘤组织中生成胶质母细胞瘤类器官 (GBO) 的详细程序。通过保留细胞-细胞相互作用并最小化克隆选择,GBO 保持亲本肿瘤的细胞异质性。我们包括有关如何传代和冷冻保存 GBO 以继续使用、生物库和长期恢复的详细信息。此外,我们描述了通过将 GBO 与嵌合抗原受体 (CAR) T 细胞共培养来研究患者对免疫疗法的特异性反应的程序。使用此方案生成 GBO 大约需要 2-4 周,而进行 CAR T 细胞共培养则需要 5-7 天。需要具备人体细胞培养、组织处理、免疫组织化学和显微镜的能力才能获得最佳结果。