Liprin-α/SYD-2 determines the size of dense projections in presynaptic active zones inC. elegans

2013 ◽  
Vol 143 (1) ◽  
pp. 1431OIA55
Author(s):  
Maike Kittelmann ◽  
Jan Hegermann ◽  
Alexandr Goncharov ◽  
Hidenori Taru ◽  
Mark H. Ellisman ◽  
...  
1983 ◽  
Vol 218 (1211) ◽  
pp. 253-258 ◽  

The morphological mechanisms involved in translocation of the synaptic vesicle to the presynaptic membrane, release of transmitter from the vesicle and recycling of the vesicle membrane are still far from understood. However, there is strong evidence that vesicles move along the surfaces of a specific set of highly labile presynaptic microtubules that direct the vesicles to the active zones. These microtubules are focused in a precise geometrical array, which is in register with and in contact with presynaptic dense projections of the central nervous system synapse or presynaptic dense bars of the motor endplate. These dense complexes constitute the presynaptic grid or active zones. The regular arrays of dense projections or bars are in turn coincident with rings or chains of synaptic vesicles mobilized at release sites on the presynaptic membrane (having arrived at these precise points by microtubule translocation). Thus it is suggested that the presynaptic microtubules not only translocate synaptic vesicles, but because of their ordered arrays determine, in ontogeny, the ordered structure of the presynaptic grid.


2013 ◽  
Vol 203 (5) ◽  
pp. 849-863 ◽  
Author(s):  
Maike Kittelmann ◽  
Jan Hegermann ◽  
Alexandr Goncharov ◽  
Hidenori Taru ◽  
Mark H. Ellisman ◽  
...  

Synaptic vesicle (SV) release is spatially and temporally regulated by a network of proteins that form the presynaptic active zone (AZ). The hallmark of most AZs is an electron-dense projection (DP) surrounded by SVs. Despite their importance for our understanding of triggered SV release, high-resolution analyses of DP structures are limited. Using electron microscopy, we show that DPs at Caenorhabditis elegans neuromuscular junctions (NMJs) were highly structured, composed of building units forming bays in which SVs are docked to the AZ membrane. Furthermore, larger ribbonlike DPs that were multimers of the NMJ building unit are found at synapses between inter- and motoneurons. We also demonstrate that DP size is determined by the activity of the AZ protein SYD-2/Liprin-α. Whereas loss of syd-2 function led to smaller DPs, syd-2 gain-of-function mutants displayed larger ribbonlike DPs through increased recruitment of ELKS-1/ELKS. Therefore, our data suggest that a main role of SYD-2/Liprin-α in synaptogenesis is to regulate the polymerization of DPs.


2015 ◽  
pp. 26-30
Author(s):  
A. V. Podnebesnykh ◽  
S. V. Kuznetsov ◽  
V. P. Ovchinnikov

On the example of the group of fields in the West Siberia North the basic types of secondary changes in reservoir rocks are reviewed. Some of the most common types of such changes in the West Siberian plate territory include the processes of zeolitization, carbonation and leaching. These processes have, as a rule, a regional character of distribution and are confined to the tectonically active zones of the earth's crust. Due to formation of different mineral paragenesises the secondary processes differently affect the reservoir rocks porosity and permeability: thus, zeolitization and carbonization promote to reducing the porosity and permeability and leaching improvement. All this, ultimately leads to a change of the oil recovery factor and hydrocarbons production levels. Study and taking into account of the reservoir rocks secondary change processes can considerably influence on placement of operating well stock and on planning of geological and technological actions.


1993 ◽  
Vol 58 (3) ◽  
pp. 496-505
Author(s):  
Ondřej Wein

Partial blocking of the transport surface under the stagnant (nerst) layer is simulated by periodically alternating bands of perfectly insulating zones and active zones with a constant potential of driving force. The numeric solution of the corresponding two-dimensional elliptic problem is represented by a simple empirical correlation for the transfer coefficients. The result is interpreted in terms of a simple electrochemical problem about limiting diffusion currents at electrodes with non-uniform surface activity.


Neuron ◽  
2006 ◽  
Vol 51 (2) ◽  
pp. 275 ◽  
Author(s):  
Dhananjay A. Wagh ◽  
Tobias M. Rasse ◽  
Esther Asan ◽  
Alois Hofbauer ◽  
Isabell Schwenkert ◽  
...  

1982 ◽  
Vol 94 (1) ◽  
pp. 88-96 ◽  
Author(s):  
G P Miljanich ◽  
A R Brasier ◽  
R B Kelly

During transmitter release, synaptic vesicle membrane is specifically inserted into the nerve terminal plasma membrane only at specialized sites or "active zones." In an attempt to obtain a membrane fraction enriched in active zones, we have utilized the electric organ of the marine ray. From this organ, a fraction enriched in nerve terminals (synaptosomes) was prepared by conventional means. These synaptosomes were bound to microscopic beads by an antiserum to purified electric organ synaptic vesicles (anti-SV). The success of this immunoadsorption procedure was demonstrated by increased specific activities of bead-bound nerve terminal cytoplasmic markers and decreased specific activities of markers for contaminating membranes. To obtain a presynaptic plasma membrane (PSPM) fraction, we lysed the bead-bound synaptosomes by hypoosmotic shock and sonication, resulting in complete release of cytoplasmic markers. When the synaptosomal fraction was surface-labeled with iodine before immunoadsorption, 10% of this label remained bead-bound after lysis, compared with 2% of the total protein, indicating an approximately fivefold enrichment of bead-bound plasma membrane. Concomitantly, the specific activity of bead-bound anti-SV increased approximately 30-fold, indicating an enrichment of plasma membrane which contained inserted synaptic vesicle components. This PSPM preparation is not simply synaptic vesicle membrane since two-dimensional electrophoresis revealed that the polypeptides of the surface-iodinated PSPM preparation include both vesicle and numerous nonvesicle components. Secondly, antiserum to the PSPM fraction is markedly different from anti-SV and binds to external, nonvesicle, nerve terminal components.


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