Microgravity-cultured glioblastoma organoids integrated with microfluidic chip for CAR-γδ T evaluation.
Ontology highlight
ABSTRACT: Tumor organoids mimicking the tumor microenvironment (TME) are key tools for tumor immunity research and personalized cancer therapy development. We integrated microgravity culture with microfluidic chip technology (Micro-GRA& FLU) to establish a platform for evaluating chimeric antigen receptor (CAR)-γδ T cell efficacy under physiological-like conditions. Patient-derived glioblastoma (GBM) cells were microgravity-cultured into glioblastoma organoids (GBOs). Pathological analysis validated GBO similarity to matched GBM in immune cell phenotypes. Microfluidic chips assessed CAR-γδ T cell cytotoxicity against GBOs. The low-cost, easy-to-operate microgravity system generated viable, uniform GBOs that retained GBM TME features. CAR-γδ T cells showed strong cytotoxicity against GBOs in microflu
SUBMITTER: Zhu G
PROVIDER: S-EPMC12717136 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA