IHEM   20887
INSTITUTO DE HISTOLOGIA Y EMBRIOLOGIA DE MENDOZA DR. MARIO H. BURGOS
Unidad Ejecutora - UE
artículos
Título:
Autophagy in Protists
Autor/es:
M DUSZENKO, M GINGER, A BRENNAND,M GUALDRÓN-LÓPEZ, M COLOMBO, G COOMBS,COPPENS, B JAYABALASINGHAM, G LANGSLEY,S DE CASTRO, R MENNA-BARRETO, J MOTTRAM, M NAVARRO, D RIGDEN, P ROMANO, V STOKA,B TURK AND P MICHELS
Revista:
AUTOPHAGY
Editorial:
LANDES BIOSCIENCE
Referencias:
Año: 2010 vol. 7 p. 127 - 158
ISSN:
1554-8627
Resumen:
‘Autophagy’ is the degradative process by which eukaryotic cells digest their own components using acid hydrolases within the lysosome. Originally thought to provide 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 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 utilise 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, suggests 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.