Center for Alternatives to Animal Testing (CAAT), Johns Hopkins University, Baltimore, MD, USA.
European Commission, Joint Research Centre (JRC), Ispra, Italy.
ALTEX. 2018;35(3):353-378. doi: 10.14573/altex.1710081. Epub 2018 Apr 13.
A major reason for the current reproducibility crisis in the life sciences is the poor implementation of quality control measures and reporting standards. Improvement is needed, especially regarding increasingly complex in vitro methods. Good Cell Culture Practice (GCCP) was an effort from 1996 to 2005 to develop such minimum quality standards also applicable in academia. This paper summarizes recent key developments in in vitro cell culture and addresses the issues resulting for GCCP, e.g. the development of induced pluripotent stem cells (iPSCs) and gene-edited cells. It further deals with human stem-cell-derived models and bioengineering of organo-typic cell cultures, including organoids, organ-on-chip and human-on-chip approaches. Commercial vendors and cell banks have made human primary cells more widely available over the last decade, increasing their use, but also requiring specific guidance as to GCCP. The characterization of cell culture systems including high-content imaging and high-throughput measurement technologies increasingly combined with more complex cell and tissue cultures represent a further challenge for GCCP. The increasing use of gene editing techniques to generate and modify in vitro culture models also requires discussion of its impact on GCCP. International (often varying) legislations and market forces originating from the commercialization of cell and tissue products and technologies are further impacting on the need for the use of GCCP. This report summarizes the recommendations of the second of two workshops, held in Germany in December 2015, aiming map the challenge and organize the process or developing a revised GCCP 2.0.
生命科学领域当前再现性危机的一个主要原因是质量控制措施和报告标准执行不力。需要进行改进,尤其是针对日益复杂的体外方法。良好的细胞培养实践(GCCP)是 1996 年至 2005 年期间制定最低质量标准的努力,这些标准也适用于学术界。本文总结了最近体外细胞培养的关键进展,并针对 GCCP 出现的问题进行了讨论,例如诱导多能干细胞(iPSC)和基因编辑细胞的发展。它还涉及人类干细胞衍生模型和器官型细胞培养的生物工程,包括类器官、器官芯片和人在芯片方法。在过去十年中,商业供应商和细胞库使人类原代细胞的应用更加广泛,增加了其使用量,但也需要针对 GCCP 提供具体的指导。包括高内涵成像和高通量测量技术在内的细胞培养系统的特性,越来越多地与更复杂的细胞和组织培养相结合,这对 GCCP 提出了进一步的挑战。基因编辑技术的广泛应用来生成和修改体外培养模型也需要讨论其对 GCCP 的影响。国际(通常是不同的)法规和源于细胞和组织产品和技术商业化的市场力量,进一步影响了使用 GCCP 的需求。本报告总结了第二次研讨会的建议,该研讨会于 2015 年 12 月在德国举行,旨在描绘挑战并组织制定修订后的 GCCP 2.0 的过程。