Interfaculty Institute for Biochemistry, University of Tübingen, Tübingen, Germany.
Autophagy. 2011 Feb;7(2):127-58. doi: 10.4161/auto.7.2.13310. Epub 2011 Feb 1.
Autophagy is the degradative process by which eukaryotic cells digest their own components using acid hydrolases within the lysosome. Originally thought to function almost exclusively in providing starving cells with nutrients taken from their own cellular constituents, autophagy is in fact involved in numerous cellular events including differentiation, turnover of macromolecules and organelles, and defense against parasitic invaders. During the last 10-20 years, molecular components of the autophagic machinery have been discovered, revealing a complex interactome of proteins and lipids, which, in a concerted way, induce membrane formation to engulf cellular material and target it for lysosomal degradation. Here, our emphasis is autophagy in protists. We discuss experimental and genomic data indicating that the canonical autophagy machinery characterized in animals and fungi appeared prior to the radiation of major eukaryotic lineages. Moreover, we describe how comparative bioinformatics revealed that this canonical machinery has been subject to moderation, outright loss or elaboration on multiple occasions in protist lineages, most probably as a consequence of diverse lifestyle adaptations. We also review experimental studies illustrating how several pathogenic protists either utilize autophagy mechanisms or manipulate host-cell autophagy in order to establish or maintain infection within a host. The essentiality of autophagy for the pathogenicity of many parasites, and the unique features of some of the autophagy-related proteins involved, suggest possible new targets for drug discovery. Further studies of the molecular details of autophagy in protists will undoubtedly enhance our understanding of the diversity and complexity of this cellular phenomenon and the opportunities it offers as a drug target.
自噬是真核细胞利用溶酶体中的酸水解酶消化自身成分的降解过程。最初认为自噬几乎完全是为了给饥饿的细胞提供营养,这些营养来自于自身细胞成分,但实际上自噬参与了许多细胞事件,包括分化、大分子和细胞器的更新以及抵御寄生虫入侵。在过去的 10-20 年中,自噬机制的分子成分已经被发现,揭示了一个复杂的蛋白质和脂质相互作用网络,它们协同诱导膜的形成,吞噬细胞物质并将其靶向溶酶体降解。在这里,我们重点讨论原生动物中的自噬。我们讨论了实验和基因组数据,表明在主要真核生物谱系辐射之前,就已经出现了动物和真菌中所描述的典型自噬机制。此外,我们还描述了比较生物信息学如何揭示这种典型的机制已经在原生动物谱系中多次被修饰、完全丢失或复杂化,这很可能是由于不同生活方式的适应。我们还回顾了一些实验研究,这些研究说明了几种致病原生动物是如何利用自噬机制或操纵宿主细胞的自噬,以在宿主中建立或维持感染。自噬对于许多寄生虫的致病性的重要性,以及参与其中的一些自噬相关蛋白的独特特征,表明可能有新的药物发现靶点。进一步研究原生动物中自噬的分子细节无疑将增强我们对这种细胞现象的多样性和复杂性的理解,并为其作为药物靶点提供机会。