1. Membrane origin for autophagy - PubMed (original) (raw)

Review

1. Membrane origin for autophagy

Fulvio Reggiori. Curr Top Dev Biol. 2006.

Abstract

Autophagy is a degradative transport route conserved among all eukaryotic organisms. During starvation, cytoplasmic components are randomly sequestered into large double-membrane vesicles called autophagosomes and delivered into the lysosome/vacuole where they are destroyed. Cells are able to modulate autophagy in response to their needs, and under certain circumstances, cargoes, such as aberrant protein aggregates, organelles, and bacteria can be selectively and exclusively incorporated into autophagosomes. As a result, this pathway plays an active role in many physiological processes, and it is induced in numerous pathological situations because of its ability to rapidly eliminate unwanted structures. Despite the advances in understanding the functions of autophagy and the identification of several factors, named Atg proteins that mediate it, the mechanism that leads to autophagosome formation is still a mystery. A major challenge in unveiling this process arises from the fact that the origin and the transport mode of the lipids employed to compose these structures is unknown. This compendium will review and analyze the current data about the possible membrane source(s) with a particular emphasis on the yeast Saccharomyces cerevisiae, the leading model organism for the study of autophagosome biogenesis, and on mammalian cells. The information acquired investigating the pathogens that subvert autophagy in order to replicate in the host cells will also be discussed because it could provide important hints for solving this mystery.

PubMed Disclaimer

Figures

Figure 1

Conceptual model for autophagy. The basic mechanism of autophagy is the sequestration of the cargo material (bulk cytoplasm, protein aggregates, organelles, or pathogens) by a cytosolic double‐membrane vesicle named an autophagosome. Extracellular stimuli or the recognition of a specific intracellular cargo induce the expansion of the isolation membrane. Upon vesicle completion, the autophagosome docks with the lysosome/vacuole and successively fuses with it. In this way the inner vesicle is liberated inside the vacuole where it is finally consumed together with the cargo by resident hydrolases. This schematic represents nonspecific autophagy and does not show specific types of autophagy including the Cvt pathway.

Figure 2

Autophagosome maturation in mammalian cells. Once sealed, the autophagosome (or AVi) fuses with endosome‐ and/or TGN‐derived transport vesicles and the MVB becoming an amphisome (or early AVd). This event leads to the acquisition of hydrolytic enzymes that initiate the consumption of the autophagosome cargo. The amphisome then fuses with a lysosome generating a new organelle termed autolysosome (or late AVd) where the degradation of the content of the initial autophagosome is completed.

References

1. Abeliovich H., Darsow T., Emr S.D. Cytoplasm to vacuole trafficking of aminopeptidase I requires a t‐SNARE‐Sec1p complex composed of Tlg2p and Vps45p. EMBO J. 1999;18:6005–6016. - PMC - PubMed
1. Abeliovich H., Dunn W.A., Jr., Kim J., Klionsky D.J. Dissection of autophagosome biogenesis into distinct nucleation and expansion steps. J. Cell Biol. 2000;151:1025–1034. - PMC - PubMed
1. Amer A.O., Swanson M.S. Autophagy is an immediate macrophage response to Legionella pneumophila. Cell. Microbiol. 2005;7:765–778. - PMC - PubMed
1. Ano Y., Hattori T., Oku M., Mukaiyama H., Baba M., Ohsumi Y., Kato N., Sakai Y. A sorting nexin PpAtg24 regulates vacuolar membrane dynamics during pexophagy via binding to phosphatidylinositol‐3‐phosphate. Mol. Biol. Cell. 2005;16:446–457. - PMC - PubMed
1. Aplin A., Jasionowski T., Tuttle D.L., Lenk S.E., Dunn W.A., Jr. Cytoskeletal elements are required for the formation and maturation of autophagic vacuoles. J. Cell. Physiol. 1992;152:458–466. - PubMed

1. Membrane origin for autophagy - PubMed (original) (raw)