{"title":"Acoustic virtual 3D scaffold for direct-interacting tumor organoid–immune cell coculture systems","authors":"Han Shan, Maike Chen, Shuang Zhao, Xiongwei Wei, Mingde Zheng, Yixin Li, Qibo Lin, Zixi Jiang, Ziyan Chen, Chunlong Fei, Zhaoxi Li, Zeyu Chen, Xiang Chen","doi":"10.1126/sciadv.adr4831","DOIUrl":null,"url":null,"abstract":"<div >Three-dimensional (3D) cell culture has revolutionized life sciences, particularly in organoid technologies. Traditional bioscaffold materials, however, complicate the detachment of tumor organoids and hamper the routine use of organoid–immune cell cocultures. Here, we show an acoustic virtual 3D scaffold (AV-Scaf) method to achieve 3D tumor organoid culture, enabling a direct-interacting tumor organoid–immune cell coculture system. The self-organization process of tumor cells is facilitated by a vortex acoustic field, which enables the cell bioassembly and ion channel activation. This approach can significantly enhance the influx of calcium ions, thereby accelerating intercellular interactions of cellular assemblies. We established scaffold-free melanoma and breast cancer organoids using AV-Scaf and cocultured melanoma organoids with T cells. We found that our coculture system resulted in a high activation state of T cells, characterized by notable up-regulation of granzyme B (2.82 to 17.5%) and interferon-γ (1.36 to 16%). AV-Scaf offers an efficient method for tumor organoid–immune cell studies, advancing cancer research and immunotherapy development.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"10 47","pages":""},"PeriodicalIF":11.7000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11584020/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.adr4831","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Three-dimensional (3D) cell culture has revolutionized life sciences, particularly in organoid technologies. Traditional bioscaffold materials, however, complicate the detachment of tumor organoids and hamper the routine use of organoid–immune cell cocultures. Here, we show an acoustic virtual 3D scaffold (AV-Scaf) method to achieve 3D tumor organoid culture, enabling a direct-interacting tumor organoid–immune cell coculture system. The self-organization process of tumor cells is facilitated by a vortex acoustic field, which enables the cell bioassembly and ion channel activation. This approach can significantly enhance the influx of calcium ions, thereby accelerating intercellular interactions of cellular assemblies. We established scaffold-free melanoma and breast cancer organoids using AV-Scaf and cocultured melanoma organoids with T cells. We found that our coculture system resulted in a high activation state of T cells, characterized by notable up-regulation of granzyme B (2.82 to 17.5%) and interferon-γ (1.36 to 16%). AV-Scaf offers an efficient method for tumor organoid–immune cell studies, advancing cancer research and immunotherapy development.
三维(3D)细胞培养给生命科学,尤其是类器官技术带来了革命性的变化。然而,传统的生物支架材料使肿瘤类器官的分离变得复杂,妨碍了类器官-免疫细胞共培养的常规使用。在这里,我们展示了一种声学虚拟三维支架(AV-Scaf)方法来实现三维肿瘤类器官培养,使肿瘤类器官-免疫细胞共培养系统能够直接相互作用。涡旋声场促进了肿瘤细胞的自组织过程,实现了细胞的生物组装和离子通道激活。这种方法可以大大增强钙离子的流入,从而加速细胞组装的细胞间相互作用。我们利用 AV-Scaf 建立了无支架的黑色素瘤和乳腺癌器官组织,并将黑色素瘤器官组织与 T 细胞进行了共培养。我们发现,我们的共培养系统导致了 T 细胞的高度活化状态,其特点是颗粒酶 B(2.82%-17.5%)和干扰素-γ(1.36%-16%)显著上调。AV-Scaf 为肿瘤类器官-免疫细胞研究提供了一种有效的方法,推动了癌症研究和免疫疗法的开发。
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.