The neuronal form of adaptor protein-3 is required for synaptic vesicle formation from endosomes

被引:72
作者
Blumstein, J
Faundez, V
Nakatsu, F
Saito, T
Ohno, H
Kelly, RB [1 ]
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[2] Emory Univ, Dept Cell Biol, Atlanta, GA 30322 USA
[3] Kanazawa Univ, Canc Res Inst, Div Mol Membrane Biol, Kanazawa, Ishikawa 9200934, Japan
[4] Chiba Univ, Grad Sch Med, Dept Mol Genet, Chiba 2608670, Japan
关键词
adaptor protein; synaptic vesicle; AP-3; endosome; brain; neuronal isoforms;
D O I
10.1523/JNEUROSCI.21-20-08034.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Heterotetrameric adaptor complexes vesiculate donor membranes. One of the adaptor protein complexes, AP-3, is present in two forms; one form is expressed in all tissues of the body, whereas the other is restricted to brain. Mice lacking both the ubiquitous and neuronal forms of AP-3 exhibit neurological disorders that are not observed in mice that are mutant only in the ubiquitous form. To begin to understand the role of neuronal AP-3 in neurological disease, we investigated its function in in vitro assays as well as its localization in neural tissue. In the presence of GTP gammaS both ubiquitous and neuronal forms of AP-3 can bind to purified synaptic vesicles. However, only the neuronal form of AP-3 can produce synaptic vesicles from endosomes in vitro. We also identified that the expression of neuronal AP-3 is limited to varicosities of neuronal-like processes and is expressed in most axons of the brain. Although the AP-2/clathrin pathway is the major route of vesicle production and the relatively minor neuronal AP-3 pathway is not necessary for viability, the absence of the latter could lead to the neurological abnormalities seen in mice lacking the expression of AP-3 in brain. In this study we have identified the first brain-specific function for a neuronal adaptor complex.
引用
收藏
页码:8034 / 8042
页数:9
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