Institut de Recherche en Immunologie et en Cancérologie, Université de Montréal.
Terry Fox Laboratory, British Columbia Cancer Agency.
J Vis Exp. 2023 Jul 21(197). doi: 10.3791/64770.
The advancement of cell transplantation approaches requires model systems that allow an accurate assessment of transplanted cell functional potency. For the central nervous system, although xenotransplantation remains state-of-the-art, such models are technically challenging, limited in throughput, and expensive. Moreover, the environmental signals present do not perfectly cross-react with human cells. This paper presents an inexpensive, accessible, and high-throughput-compatible model for the transplantation and tracking of human neural cells into human cerebral organoids. These organoids can be easily generated from human induced pluripotent stem cells using commercial kits and contain the key cell types of the cerebrum. We first demonstrate this transplant protocol with the injection of EGFP-labeled human iPSC-derived neural progenitor cells (NPCs) into these organoids. We next discuss considerations for tracking the growth of these cells in the organoid by live-cell fluorescence microscopy and demonstrate the tracking of transplanted EGFP-labeled NPCs in an organoid over a 4 month period. Finally, we present a protocol for the sectioning, cyclic immunofluorescent staining, and imaging of the transplanted cells in their local context. The organoid transplantation model presented here allows the long-term (at least 4 months) tracking of transplanted human cells directly in a human microenvironment with an inexpensive and simple-to-perform protocol. It, thus, represents a useful model both for neural cell therapies (transplants) and, likely, for modeling central nervous system (CNS) tumors in a more microenvironmentally accurate manner.
细胞移植方法的进步需要模型系统,这些系统可以准确评估移植细胞的功能效力。对于中枢神经系统,虽然异种移植仍然是最先进的,但这些模型在技术上具有挑战性、通量有限且昂贵。此外,存在的环境信号与人类细胞不完全交叉反应。本文提出了一种廉价、可及且与高通量兼容的模型,用于将人类神经细胞移植和追踪到人类大脑类器官中。这些类器官可以使用商业试剂盒从人类诱导多能干细胞轻松生成,并且包含大脑的关键细胞类型。我们首先使用 EGFP 标记的人类 iPSC 衍生的神经祖细胞 (NPC) 注射到这些类器官中来演示这种移植方案。接下来,我们讨论了通过活细胞荧光显微镜追踪这些细胞在类器官中的生长的注意事项,并展示了在 4 个月的时间内追踪移植的 EGFP 标记 NPC 在类器官中的生长情况。最后,我们提出了一种用于在其局部环境中对移植细胞进行切片、循环免疫荧光染色和成像的方案。这里提出的类器官移植模型允许使用一种廉价且易于执行的方案,直接在人类微环境中对移植的人类细胞进行长期(至少 4 个月)追踪。因此,它代表了神经细胞疗法(移植)的有用模型,并且可能更准确地模拟中枢神经系统 (CNS) 肿瘤。