Bertillot Fabien, Attieh Youmna, Delarue Morgan, Gurchenkov Basile G, Descroix Stephanie, Vignjevic Danijela Matic, Ferraro Davide
Institut Curie, PSL Research University, CNRS, UMR 144, 12 rue Lhomond, 75005, Paris, France.
Physics Department, University of California, Berkeley, CA, USA.
Methods Mol Biol. 2017;1612:269-279. doi: 10.1007/978-1-4939-7021-6_20.
During tumor progression, cancer cells acquire the ability to escape the primary tumor and invade adjacent tissues. They migrate through the stroma to reach blood or lymphatics vessels that will allow them to disseminate throughout the body and form metastasis at distant organs. To assay invasion capacity of cells in vitro, multicellular spheroids of cancer cells, mimicking primary tumor, are commonly embedded in collagen I extracellular matrix, which mimics the stroma. However, due to their higher density, spheroids tend to sink at the bottom of the collagen droplets, resulting in the spreading of the cells on two dimensions. We developed an innovative method based on droplet microfluidics to embed and control the position of multicellular spheroids inside spherical droplets of collagen. In this method cancer cells are exposed to a uniform three-dimensional (3D) collagen environment resulting in 3D cell invasion.
在肿瘤进展过程中,癌细胞获得了逃离原发肿瘤并侵入邻近组织的能力。它们穿过基质到达血管或淋巴管,这些血管和淋巴管会使癌细胞扩散到全身并在远处器官形成转移灶。为了在体外检测细胞的侵袭能力,通常将模拟原发肿瘤的癌细胞多细胞球体嵌入模拟基质的I型胶原细胞外基质中。然而,由于球体密度较高,它们往往会沉到胶原液滴底部,导致细胞在二维平面上扩散。我们开发了一种基于液滴微流控的创新方法,用于在球形胶原液滴中嵌入并控制多细胞球体的位置。在这种方法中,癌细胞暴露于均匀的三维(3D)胶原环境中,从而实现3D细胞侵袭。