Folch Albert
Department of Biomedical Engineering, University of Washington, Seattle, WA, USA.
J Vis Exp. 2007(8):300. doi: 10.3791/300. Epub 2007 Oct 1.
The ability to culture cells has revolutionized hypothesis testing in basic cell and molecular biology research. It has become a standard methodology in drug screening, toxicology, and clinical assays, and is increasingly used in regenerative medicine. However, the traditional cell culture methodology essentially consisting of the immersion of a large population of cells in a homogeneous fluid medium and on a homogeneous flat substrate has become increasingly limiting both from a fundamental and practical perspective. Microfabrication technologies have enabled researchers to design, with micrometer control, the biochemical composition and topology of the substrate, and the medium composition, as well as the neighboring cell type in the surrounding cellular microenvironment. Additionally, microtechnology is conceptually well-suited for the development of fast, low-cost in vitro systems that allow for high-throughput culturing and analysis of cells under large numbers of conditions. In this interview, Albert Folch explains these limitations, how they can be overcome with soft lithography and microfluidics, and describes some relevant examples of research in his lab and future directions.
细胞培养能力彻底改变了基础细胞和分子生物学研究中的假设检验。它已成为药物筛选、毒理学和临床检测的标准方法,并越来越多地应用于再生医学。然而,传统的细胞培养方法主要是将大量细胞浸没在均匀的流体培养基中,并置于均匀的平坦基质上,从基础和实际角度来看,这种方法的局限性越来越大。微纳加工技术使研究人员能够以微米级的精度控制设计基质的生化组成和拓扑结构、培养基成分以及周围细胞微环境中的相邻细胞类型。此外,微技术在概念上非常适合开发快速、低成本的体外系统,该系统能够在大量条件下对细胞进行高通量培养和分析。在本次访谈中,阿尔伯特·福尔克解释了这些局限性、如何通过软光刻和微流控技术克服这些局限性,并介绍了他实验室的一些相关研究实例和未来方向。