Roles of ATP in depletion and replenishment of the releasable pool of synaptic vesicles

被引:73
作者
Heidelberger, R
Sterling, P
Matthews, G
机构
[1] Univ Texas, Sch Med, Dept Neurobiol & Anat, Houston, TX 77030 USA
[2] Univ Texas, Sch Med, WM Keck Ctr Neurobiol Learning & Memory, Houston, TX 77030 USA
[3] Univ Penn, Dept Neurosci, Philadelphia, PA 19104 USA
[4] SUNY Stony Brook, Dept Neurobiol & Behav, Stony Brook, NY 11794 USA
关键词
D O I
10.1152/jn.2002.88.1.98
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synaptic terminals of retinal bipolar neurons contain a pool of readily releasable synaptic vesicles that undergo rapid calcium-dependent release. ATP hydrolysis is required for the functional refilling of this vesicle pool. However, it was unclear which steps required ATP hydrolysis: delivery of vesicles to their anatomical release sites or preparation of synaptic vesicles and/or the secretory apparatus for fusion. To address this, we dialyzed single synaptic terminals with ATP or the poorly hydrolyzable analogue ATP-gammaS and examined the size of the releasable pool, refilling of the releasable pool, and the number of vesicles at anatomical active zones. After minutes of dialysis with ATP-gammaS, vesicles already in the releasable pool could still be discharged. This pool was not functionally refilled despite the fact that its anatomical correlate, the number of synaptic vesicles tethered to active zone synaptic ribbons, was completely normal. We conclude 1) because the existing releasable pool is stable during prolonged inhibition of ATP hydrolysis, whereas entry into the functional pool is blocked, a vesicle on entering the pool will tend to remain there until it fuses; 2) because the anatomical pool is unaffected by inhibition of ATP hydrolysis, failure to refill the functional pool is not caused by failure of vesicle movement; 3) local vesicle movements important for pool refilling and fusion are independent of conventional ATP-dependent motor proteins; and 4) ATP hydrolysis is required for the biochemical transition of vesicles and/or release sites to fusion-competent status.
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页码:98 / 106
页数:9
相关论文
共 62 条
[1]   CAPS (mammalian UNC-31) protein localizes to membranes involved in dense-core vesicle exocytosis [J].
Berwin, B ;
Floor, E ;
Martin, TFJ .
NEURON, 1998, 21 (01) :137-145
[2]   Kinesin- and myosin-driven steps of vesicle recruitment for Ca2+-regulated exocytosis [J].
Bi, GQ ;
Morris, RL ;
Liao, GC ;
Alderton, JM ;
Scholey, JM ;
Steinhardt, RA .
JOURNAL OF CELL BIOLOGY, 1997, 138 (05) :999-1008
[3]   A genomic perspective on membrane compartment organization [J].
Bock, JB ;
Matern, HT ;
Peden, AA ;
Scheller, RH .
NATURE, 2001, 409 (6822) :839-841
[4]   Differential expression of the presynaptic cytomatrix protein bassoon among ribbon synapses in the mammalian retina [J].
Brandstätter, JH ;
Fletcher, EL ;
Garner, CC ;
Gundelfinger, ED ;
Wässle, H .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (10) :3683-3693
[5]   ENZYMATIC DIGESTION OF SYNAPTIC RIBBONS IN AMPHIBIAN RETINAL PHOTORECEPTORS [J].
BUNT, AH .
BRAIN RESEARCH, 1971, 25 (03) :571-+
[6]   RELAXATION OF MUSCLE-FIBERS WITH ADENOSINE 5'-[GAMMA-THIO]TRIPHOSPHATE (ATP[GAMMA-S]) AND BY LASER PHOTOLYSIS OF CAGED ATP[GAMMA-S] - EVIDENCE FOR CA-2+-DEPENDENT AFFINITY OF RAPIDLY DETACHING ZERO-FORCE CROSS-BRIDGES [J].
DANTZIG, JA ;
WALKER, JW ;
TRENTHAM, DR ;
GOLDMAN, YE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (18) :6716-6720
[7]   Localization of the presynaptic cytomatrix protein piccolo at ribbon and conventional synapses in the rat retina:: Comparison with bassoon [J].
Dick, O ;
Hack, I ;
Altrock, WD ;
Garner, CC ;
Gundelfinger, ED ;
Brandstätter, JH .
JOURNAL OF COMPARATIVE NEUROLOGY, 2001, 439 (02) :224-234
[8]  
Gillis Kevin D., 1995, P155
[9]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[10]   Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy [J].
Hanson, PI ;
Roth, R ;
Morisaki, H ;
Jahn, R ;
Heuser, JE .
CELL, 1997, 90 (03) :523-535