Humbert Magali, Morán María, de la Cruz-Ojeda Patricia, Muntané Jordi, Wiedmer Tabea, Apostolova Nadezda, McKenna Sharon L, Velasco Guillermo, Balduini Walter, Eckhart Leopold, Janji Bassam, Sampaio-Marques Belém, Ludovico Paula, Žerovnik Eva, Langer Rupert, Perren Aurel, Engedal Nikolai, Tschan Mario P
TRANSAUTOPHAGY: European Network for Multidisciplinary Research and Translation of Autophagy Knowledge, COST Action CA15138, 08193 Barcelona, Spain.
Institute of Pathology, University of Bern, Murtenstrasse 31, CH-3008 Bern, Switzerland.
Biology (Basel). 2020 Mar 21;9(3):59. doi: 10.3390/biology9030059.
Autophagy is a highly conserved degradation mechanism that is essential for maintaining cellular homeostasis. In human disease, autophagy pathways are frequently deregulated and there is immense interest in targeting autophagy for therapeutic approaches. Accordingly, there is a need to determine autophagic activity in human tissues, an endeavor that is hampered by the fact that autophagy is characterized by the flux of substrates whereas histology informs only about amounts and localization of substrates and regulators at a single timepoint. Despite this challenging task, considerable progress in establishing markers of autophagy has been made in recent years. The importance of establishing clear-cut autophagy markers that can be used for tissue analysis cannot be underestimated. In this review, we attempt to summarize known techniques to quantify autophagy in human tissue and their drawbacks. Furthermore, we provide some recommendations that should be taken into consideration to improve the reliability and the interpretation of autophagy biomarkers in human tissue samples.
自噬是一种高度保守的降解机制,对维持细胞内稳态至关重要。在人类疾病中,自噬途径常常失调,因此针对自噬进行治疗的方法备受关注。因此,有必要确定人体组织中的自噬活性,但这一努力受到以下事实的阻碍:自噬的特征是底物的通量,而组织学仅能在单个时间点告知底物和调节因子的数量及定位。尽管这项任务具有挑战性,但近年来在建立自噬标志物方面已取得了相当大的进展。建立可用于组织分析的明确自噬标志物的重要性不可低估。在本综述中,我们试图总结用于量化人体组织中自噬的已知技术及其缺点。此外,我们提供了一些建议,在分析人体组织样本中的自噬生物标志物时,应予以考虑以提高其可靠性和解读能力。