Université Grenoble Alpes, INSERM, CEA, BIG, F-38000 Grenoble, France.
Université Grenoble Alpes, F-38000 Grenoble, France; TIMC-IMAG/CNRS UMR 5525, F-38041 Grenoble, France.
Trends Biotechnol. 2017 Nov;35(11):1035-1048. doi: 10.1016/j.tibtech.2017.08.003. Epub 2017 Sep 17.
We highlight the disposition of various cell types to self-organize into complex organ-like structures without necessarily the support of any stromal cells, provided they are placed into permissive 3D culture conditions. The goal of generating organoids reproducibly and efficiently has been hampered by poor understanding of the exact nature of the intrinsic cell properties at the origin of organoid generation, and of the signaling pathways governing their differentiation. Using microtechnologies like microfluidics to engineer organoids would create opportunities for single-cell genomics and high-throughput functional genomics to exhaustively characterize cell intrinsic properties. A more complete understanding of the development of organoids would enhance their relevance as models to study organ morphology, function, and disease and would open new avenues in drug development and regenerative medicine.
我们强调了各种细胞类型的特性,即它们可以在没有任何基质细胞支持的情况下,自行组织成为复杂的类器官结构,只要它们被放置在允许的 3D 培养条件下。然而,由于对类器官生成中固有细胞特性的确切性质以及控制其分化的信号通路的理解不足,因此难以有效地重复生成类器官。使用微流控等微技术来设计类器官将为单细胞基因组学和高通量功能基因组学提供机会,从而详尽地描述细胞内在特性。更深入地了解类器官的发育将增强它们作为研究器官形态、功能和疾病模型的相关性,并为药物开发和再生医学开辟新途径。