Making autophagosomes: localized synthesis of phosphatidylinositol 3-phosphate holds the clue.

Abstract

Autophagy presents a topological challenge for the cell because it requires delivery of cytosolic material to the lumen of a membrane-bound compartment, the lysosome. This is solved in an ingenious way by the formation of a double-membrane vesicle, the autophagosome, which captures cytosolic proteins and organelles during its transformation from a planar membrane disk into a sphere. In this way, cytosolic material first becomes lumenal and is then delivered for degradation to the lysosome. An unsolved set of questions in autophagy concerns the membrane of the autophagosome: what are the signals for its formation and what is its identity? Recently we provided some clues that may help answer these questions. By following the dynamics of several phosphatidylinositol 3-phosphate (PI3P)-binding proteins during amino acid starvation (and autophagy induction) we concluded that at least some autophagosomes are formed in a starvation-induced, PI3P-enriched membrane compartment dynamically connected to the endoplasmic reticulum (ER). We termed the membranes of this compartment omegasomes (from their omega-like shape). Our data suggest that PI3P is important for providing localization clues and perhaps for facilitating the fusion step at the final stage of autophagosome formation.

• Authors: Simon Walker, Priya Chandra, Maria Manifava, Elizabeth Axe, Nicholas T Ktistakis
• Journal: Autophagy (Autophagy) Vol. 4 Issue 8 Pg. 1093-6 (Nov 2008) ISSN: 1554-8635 [Electronic] United States
• PMID: 18927492 (Publication Type: Journal Article)

Chemical References

• Amino Acids
• Phosphatidylinositol Phosphates
• Proteins
• phosphatidylinositol 3-phosphate

Topics

• Amino Acids (metabolism)
• Autophagy
• Cell Membrane (metabolism)
• Endoplasmic Reticulum (metabolism)
• Humans
• Phagosomes (metabolism)
• Phosphatidylinositol Phosphates (biosynthesis)
• Proteins (metabolism)