TY - JOUR
T1 - Autophagy in protists
AU - Duszenko, Michael
AU - Ginger, Michael L.
AU - Brennand, Ana
AU - Gualdrón-López, Melisa
AU - Colombo, Maria Isabel
AU - Coombs, Graham H.
AU - Coppens, Isabelle
AU - Jayabalasingham, Bamini
AU - Langsley, Gordon
AU - De Castro, Solange Lisboa
AU - Menna-Barreto, Rubem
AU - Mottram, Jeremy C.
AU - Navarro, Miguel
AU - Rigden, Daniel J.
AU - Romano, Patricia S.
AU - Stoka, Veronika
AU - Turk, Boris
AU - Michels, Paul A.M.
N1 - Funding Information:
of parasites as a result of ain the previous sections. F%dminor T.bPistration orucei, thOf DHe examPA or nple is tUeurhe kEopep-illing JTand FScienURItifiqSA) aue’ (JnFCd the BRS-FNVelgiRS) aUan Ind aFnteruniversity Attraction Poles-ssociated foundations (FRSM tides,120,121 while for T. cruzi the same was achieved with lyso-Federal Office for Scientific, Technical and Cultural Affairs for phospholipid analogues and naphtoimidazoles.127,130 However, support of their research on autophagy in trypanosomes; M.L.G. similar data regarding the induction of autophagic cell death of the Royal Society for an University Research Fellowship; G.L. the Leishmania parasites by administration of compounds are not Wellcome Trust for a Special Initiative grant (075820/A/04/Z) available. for support for ‘An integrated approach for the development of Apicomplexan parasites also undergo major morphologi-sustainable methods to control tropical theileriosis’; J.C.M. and cal changes during the differentiation between the successive G.H.C. the Medical Research Council for support (G0700127); life-cycle stages. For Plasmodium, it has been discussed above M.N. the MICINN for support (SAF2009-07587); B.T. and that, during the sporozoite-to-trophozoite conversion, important V.S. the Slovenian Research Agency for research grants (P1-0140, interior remodeling occurs involving the elimination of many J1-9520, J3-2258); S.L.d.C. and R.M.B. the Brazilian agencies organelles. Morphological analysis, in conjunction with immuno-CNPq and Faperj; M.I.C. and P.R. the ANPCYT (PICT 2005 # labeling with anti-ATG8, indicates that this conversion involves 38420) and Comisión Nacional Salud Investiga in Argentina for autophagy. Although the essentiality of autophagy for this dif-research grants; B.T. and V.S. would like to thank Vito Turk for ferentiation has not yet been demonstrated by genetic means, the valuable discussions.
PY - 2011/2
Y1 - 2011/2
N2 - 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 past 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.
AB - 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 past 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.
KW - Apicomplexa
KW - Autophagy
KW - Drug discovery
KW - Evolution
KW - Free-living protist
KW - Life-cycle differentiation
KW - Parasitic protist
KW - Pexophagy
KW - Trypanosomatidae
KW - Ubiquitination
UR - http://www.scopus.com/inward/record.url?scp=79551573171&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79551573171&partnerID=8YFLogxK
U2 - 10.4161/auto.7.2.13310
DO - 10.4161/auto.7.2.13310
M3 - Review article
C2 - 20962583
AN - SCOPUS:79551573171
SN - 1554-8627
VL - 7
SP - 127
EP - 158
JO - Autophagy
JF - Autophagy
IS - 2
ER -