Amphiphysins: Raising the BAR for synaptic vesicle recycling and membrane dynamics

被引:72
作者
Zhang, B [1 ]
Zelhof, AC
机构
[1] Univ Texas, Neurobiol Sect, Austin, TX 78712 USA
[2] Univ Texas, Sect Mol Cell & Dev Biol, Austin, TX 78712 USA
[3] Univ Texas, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[4] Univ Texas, Inst Neurosci, Austin, TX 78712 USA
[5] Univ Calif San Diego, Dept Biol, La Jolla, CA 92093 USA
关键词
actin cytoskeleton; clathrin; Drosophila; endocytosis; morphogenesis; muscle T-tubules; photoreceptor; synapse;
D O I
10.1034/j.1600-0854.2002.30702.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Amphiphysins, members of the BAR (Bin-Amphiphysin-Rvsp) protein super family, have been postulated to play a key role in clathrin-mediated endocytosis of synaptic vesicles (SVs). This review focuses on recent genetic studies of the role of amphiphysins in SV recycling and membrane morphogenesis. In the mouse, brain-specific amphiphysin I and II regulate, but are not essential for, SV recycling. The role of this regulation appears important, as mice deficient in these proteins have seizures and are deficient in learning and memory. In the fruit fly Drosophila melanogaster, amphiphysin is found in muscles and is enriched at postsynaptic membranes of neuromuscular junctions (NMJs); however, it does not play a role in SV recycling. Rather, amphiphysin in fly muscles appears to regulate the organization and structure of the muscle T-tubule system and possibly the subsynaptic reticulum. Amphiphysin is also involved in membrane organization in both neurons and non-neuronal cells in Drosophila. These studies reveal pleiotropic functions for amphiphysins in clathrin-mediated endocytosis and the regulation of membrane dynamics, perhaps through the actin cytoskeleton.
引用
收藏
页码:452 / 460
页数:9
相关论文
共 76 条
[1]   DEFINING PROTEIN INTERACTIONS WITH YEAST ACTIN IN-VIVO [J].
AMBERG, DC ;
BASART, E ;
BOTSTEIN, D .
NATURE STRUCTURAL BIOLOGY, 1995, 2 (01) :28-35
[2]   Clathrin function in yeast endocytosis [J].
Baggett, JJ ;
Wendland, B .
TRAFFIC, 2001, 2 (05) :297-302
[3]   ALTERATION OF A YEAST SH3 PROTEIN LEADS TO CONDITIONAL VIABILITY WITH DEFECTS IN CYTOSKELETAL AND BUDDING PATTERNS [J].
BAUER, F ;
URDACI, M ;
AIGLE, M ;
CROUZET, M .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (08) :5070-5084
[4]   Amphiphysin I is associated with coated endocytic intermediates and undergoes stimulation-dependent dephosphorylation in nerve terminals [J].
Bauerfeind, R ;
Takei, K ;
De Camilli, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (49) :30984-30992
[5]   QUANTITATIVE ASPECTS OF TRANSMITTER RELEASE [J].
BITTNER, GD ;
KENNEDY, D .
JOURNAL OF CELL BIOLOGY, 1970, 47 (03) :585-+
[6]  
Bon E, 2000, YEAST, V16, P1229, DOI 10.1002/1097-0061(20000930)16:13<1229::AID-YEA618>3.0.CO
[7]  
2-Q
[8]   The yeast Rvs161 and Rvs167 proteins are involved in secretory vesicles targeting the plasma membrane and in cell integrity [J].
Breton, AM ;
Schaeffer, J ;
Aigle, M .
YEAST, 2001, 18 (11) :1053-1068
[9]   Sequential steps in clathrin-mediated synaptic vesicle endocytosis [J].
Brodin, L ;
Löw, P ;
Shupliakov, O .
CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (03) :312-320
[10]   Biological basket weaving: Formation and function of clathrin-coated vesicles [J].
Brodsky, FM ;
Chen, CY ;
Knuehl, C ;
Towler, MC ;
Wakeham, DE .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2001, 17 :517-568