%0 Journal Article %1 Bhal_2004_745 %A Bhalla, Upinder S %D 2004 %J Biophys. J. %K 1, 15298883 Animals, Biological, Biology, Blotting, Calcium Calcium, Cell Comparative Complexes, Computational Computer Diffusion, Dose-Response Drug, Electric Evolution, Excitatory Factors, Fluoresceins, Fractions, Gov't, Hippocampus, Humans, In Kinase MAP Male, Membrane, Mitogen-Activated Models, Molecular, Multienzyme Neurological, Neurons, Newborn, Non-U.S. P.H.S., Phosphotransferases, Postsynaptic Potentials, Processes, Protein Proteins, Radiation, Rats, Relationship, Research SNARE Signal Signaling Signaling, Simulation, Software, Statistical, Stimulation, Stochastic Study, Subcellular Support, Synapses, Synaptic System, Time Transduction, Transmission, Transport U.S. Vesicular Vitro, Western, %N 2 %P 745--753 %R 10.1529/biophysj.104.040501 %T Signaling in small subcellular volumes. II. Stochastic and diffusion effects on synaptic network properties. %U http://dx.doi.org/10.1529/biophysj.104.040501 %V 87 %X The synaptic signaling network is capable of sophisticated cellular computations. These include the ability to respond selectively to different patterns of input, and to sustain changes in response over long periods. The small volume of the synapse complicates the analysis of signaling because the chemical environment is strongly affected by diffusion and stochasticity. This study is based on an updated version of a previously proposed synaptic signaling circuit (Bhalla and Iyengar, 1999) and analyzes three network computation properties in small volumes: bistability, thresholding, and pattern selectivity. Simulations show that although there are diffusive regimes in which bistability may persist, chemical noise at small volumes overwhelms bistability. In the deterministic situation, the network exhibits a sharp threshold for transition between lower and upper stable states. This transition is broadened and individual runs partition between lower and upper states, when stochasticity is considered. The third network property, pattern selectivity, is severely degraded at synaptic volumes. However, there are regimes in which a process similar to stochastic resonance operates and amplifies pattern selectivity. These results imply that simple scaling of signaling conditions to femtoliter volumes is unlikely, and microenvironments, such as reaction complex formation, may be essential for reliable small-volume signaling.

@article{Bhal_2004_745, abstract = {The synaptic signaling network is capable of sophisticated cellular computations. These include the ability to respond selectively to different patterns of input, and to sustain changes in response over long periods. The small volume of the synapse complicates the analysis of signaling because the chemical environment is strongly affected by diffusion and stochasticity. This study is based on an updated version of a previously proposed synaptic signaling circuit (Bhalla and Iyengar, 1999) and analyzes three network computation properties in small volumes: bistability, thresholding, and pattern selectivity. Simulations show that although there are diffusive regimes in which bistability may persist, chemical noise at small volumes overwhelms bistability. In the deterministic situation, the network exhibits a sharp threshold for transition between lower and upper stable states. This transition is broadened and individual runs partition between lower and upper states, when stochasticity is considered. The third network property, pattern selectivity, is severely degraded at synaptic volumes. However, there are regimes in which a process similar to stochastic resonance operates and amplifies pattern selectivity. These results imply that simple scaling of signaling conditions to femtoliter volumes is unlikely, and microenvironments, such as reaction complex formation, may be essential for reliable small-volume signaling.}, added-at = {2009-06-03T11:20:58.000+0200}, author = {Bhalla, Upinder S}, biburl = {https://www.bibsonomy.org/bibtex/28e07ee53c1c4b22363c9af1ea35578ed/hake}, description = {The whole bibliography file I use.}, doi = {10.1529/biophysj.104.040501}, file = {Bhal_2004_745.pdf:Bhal_2004_745.pdf:PDF}, interhash = {f4d00bf616a9f3fe187f7fdbee696a66}, intrahash = {8e07ee53c1c4b22363c9af1ea35578ed}, journal = {Biophys. J.}, keywords = {1, 15298883 Animals, Biological, Biology, Blotting, Calcium Calcium, Cell Comparative Complexes, Computational Computer Diffusion, Dose-Response Drug, Electric Evolution, Excitatory Factors, Fluoresceins, Fractions, Gov't, Hippocampus, Humans, In Kinase MAP Male, Membrane, Mitogen-Activated Models, Molecular, Multienzyme Neurological, Neurons, Newborn, Non-U.S. P.H.S., Phosphotransferases, Postsynaptic Potentials, Processes, Protein Proteins, Radiation, Rats, Relationship, Research SNARE Signal Signaling Signaling, Simulation, Software, Statistical, Stimulation, Stochastic Study, Subcellular Support, Synapses, Synaptic System, Time Transduction, Transmission, Transport U.S. Vesicular Vitro, Western,}, month = Aug, number = 2, pages = {745--753}, pii = {87/2/745}, pmid = {15298883}, timestamp = {2009-06-03T11:21:03.000+0200}, title = {Signaling in small subcellular volumes. II. Stochastic and diffusion effects on synaptic network properties.}, url = {http://dx.doi.org/10.1529/biophysj.104.040501}, volume = 87, year = 2004 }