Autophagic tubes:: Vacuolar invaginations involved in lateral membrane sorting and inverse vesicle budding

被引:137
作者
Müller, O
Sattler, T
Flötenmeyer, M
Schwarz, H
Plattner, H
Mayer, A
机构
[1] Max Planck Gesell, Friedrich Miescher Lab, D-72076 Tubingen, Germany
[2] Fachbereich Biol, D-78457 Constance, Germany
[3] Max Planck Inst Entwicklungsbiol, D-72076 Tubingen, Germany
关键词
microautophagocytosis; lysosome; yeast; proteolysis; budding;
D O I
10.1083/jcb.151.3.519
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Many intracellular compartments of eukaryotic cells do not adopt a spherical shape, which would be expected in the absence of mechanisms organizing their structure. However, little is known about the principles determining the shape of organelles. We have observed very defined structural changes of vacuoles, the lysosome equivalents of yeast. The vacuolar membrane can form a large tubular invagination from which vesicles bud off into the lumen of the organelle. Formation of the tube is regulated via the Apg/Aut pathway. Its lumen is continuous with the cytosol, making this inverse budding reaction equivalent to microautophagocytosis. The tube is highly dynamic, often branched, and defined by a sharp kink of the vacuolar membrane at the site of invagination. The tube is formed by vacuoles in an autonomous fashion. It persists after vacuole isolation and, therefore, is independent of surrounding cytoskeleton. There is a striking lateral heterogeneity along the tube, with a high density of transmembrane particles at the base and a smooth zone devoid of transmembrane particles at the tip where budding occurs. We postulate a lateral sorting mechanism along the tube that mediates a depletion of large transmembrane proteins at the tip and results in the inverse budding of Lipid-rich vesicles into the lumen of the organelle.
引用
收藏
页码:519 / 528
页数:10
相关论文
共 51 条
[1]   Cytoplasm to vacuole trafficking of aminopeptidase I requires a t-SNARE-Sec1p complex composed of Tlg2p and Vps45p [J].
Abeliovich, H ;
Darsow, T ;
Emr, SD .
EMBO JOURNAL, 1999, 18 (21) :6005-6016
[2]   Analysis of the membrane structures involved in autophagy in yeast by freeze-replica method [J].
Baba, M ;
Osumi, M ;
Ohsumi, Y .
CELL STRUCTURE AND FUNCTION, 1995, 20 (06) :465-471
[3]   ULTRASTRUCTURAL ANALYSIS OF THE AUTOPHAGIC PROCESS IN YEAST - DETECTION OF AUTOPHAGOSOMES AND THEIR CHARACTERIZATION [J].
BABA, M ;
TAKESHIGE, K ;
BABA, N ;
OHSUMI, Y .
JOURNAL OF CELL BIOLOGY, 1994, 124 (06) :903-913
[4]   Functions of lipid rafts in biological membranes [J].
Brown, DA ;
London, E .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 :111-136
[5]   Retrograde traffic out of the yeast vacuole to the TGN occurs via the prevacuolar/endosomal compartment [J].
Bryant, NJ ;
Piper, RC ;
Weisman, LS ;
Stevens, TH .
JOURNAL OF CELL BIOLOGY, 1998, 142 (03) :651-663
[6]   REGULATED IMPORT AND DEGRADATION OF A CYTOSOLIC PROTEIN IN THE YEAST VACUOLE [J].
CHIANG, HL ;
SCHEKMAN, R .
NATURE, 1991, 350 (6316) :313-318
[7]   Lysosomes, a meeting point of proteins, chaperones, and proteases [J].
Cuervo, AM ;
Dice, JF .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1998, 76 (01) :6-12
[8]   THE MICROTUBULE-DEPENDENT FORMATION OF A TUBULOVESICULAR NETWORK WITH CHARACTERISTICS OF THE ER FROM CULTURED-CELL EXTRACTS [J].
DABORA, SL ;
SHEETZ, MP .
CELL, 1988, 54 (01) :27-35
[9]   Regulation of endocytosis, exocytosis, and shape by membrane tension [J].
Dai, J ;
Sheetz, MP .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1995, 60 :567-571
[10]   A multispecificity syntaxin homologue, Vam3p, essential for autophagic and biosynthetic protein transport to the vacuole [J].
Darsow, T ;
Rieder, SE ;
Emr, SD .
JOURNAL OF CELL BIOLOGY, 1997, 138 (03) :517-529