Life Sciences Institute and Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt; Department of Experimental Oncology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Autophagy. 2021 Jan;17(1):1-382. doi: 10.1080/15548627.2020.1797280. Epub 2021 Feb 8.
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.
2008 年,我们发布了第一套标准化自噬研究的指南。自那时以来,这个主题越来越受到关注,许多科学家也进入了这个领域。我们的知识库和相关新技术也在不断扩展。因此,定期制定用于监测不同生物体中自噬的更新指南非常重要。尽管有很多综述,但对于评估自噬的可接受方法,特别是在多细胞真核生物中,仍然存在混淆。在这里,我们为研究人员提供了一套指南,用于选择和解释检查自噬和相关过程的方法,以及为评论者提供对关注这些过程的报告进行现实和合理的评论。这些指南并不是一套教条式的规则,因为任何测定方法的适当性在很大程度上取决于要提出的问题和所使用的系统。此外,没有任何单一的测定方法适用于每种情况,需要使用多种技术来正确监测每种实验条件下的自噬。最后,自噬机制的几个核心组成部分与不同的自噬过程(经典和非经典自噬)有关,这意味着阻断自噬的遗传方法应该依赖于靶向两个或更多理想地参与途径不同步骤的自噬相关基因。类似地,由于参与自噬的多种蛋白质也调节包括细胞凋亡在内的其他细胞途径,并非所有蛋白质都可以用作自噬反应的特异性标志物。在这里,我们批判性地讨论了评估自噬的当前方法以及它们可以或不能提供的信息。我们的最终目标是鼓励该领域的智力和技术创新。