↓ Skip to main content

Synaptic bouton properties are tuned to best fit the prevailing firing pattern

Overview of attention for article published in Frontiers in Computational Neuroscience, September 2014
Altmetric Badge

Citations

dimensions_citation
21 Dimensions

Readers on

mendeley
47 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Title
Synaptic bouton properties are tuned to best fit the prevailing firing pattern
Published in
Frontiers in Computational Neuroscience, September 2014
DOI 10.3389/fncom.2014.00101
Pubmed ID
Authors

Markus M. Knodel, Romina Geiger, Lihao Ge, Daniel Bucher, Alfio Grillo, Gabriel Wittum, Christoph M. Schuster, Gillian Queisser

Abstract

The morphology of presynaptic specializations can vary greatly ranging from classical single-release-site boutons in the central nervous system to boutons of various sizes harboring multiple vesicle release sites. Multi-release-site boutons can be found in several neural contexts, for example at the neuromuscular junction (NMJ) of body wall muscles of Drosophila larvae. These NMJs are built by two motor neurons forming two types of glutamatergic multi-release-site boutons with two typical diameters. However, it is unknown why these distinct nerve terminal configurations are used on the same postsynaptic muscle fiber. To systematically dissect the biophysical properties of these boutons we developed a full three-dimensional model of such boutons, their release sites and transmitter-harboring vesicles and analyzed the local vesicle dynamics of various configurations during stimulation. Here we show that the rate of transmission of a bouton is primarily limited by diffusion-based vesicle movements and that the probability of vesicle release and the size of a bouton affect bouton-performance in distinct temporal domains allowing for an optimal transmission of the neural signals at different time scales. A comparison of our in silico simulations with in vivo recordings of the natural motor pattern of both neurons revealed that the bouton properties resemble a well-tuned cooperation of the parameters release probability and bouton size, enabling a reliable transmission of the prevailing firing-pattern at diffusion-limited boutons. Our findings indicate that the prevailing firing-pattern of a neuron may determine the physiological and morphological parameters required for its synaptic terminals.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 47 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 47 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 15 32%
Student > Ph. D. Student 13 28%
Professor 3 6%
Student > Doctoral Student 3 6%
Student > Postgraduate 3 6%
Other 6 13%
Unknown 4 9%
Readers by discipline Count As %
Neuroscience 18 38%
Agricultural and Biological Sciences 16 34%
Physics and Astronomy 2 4%
Psychology 1 2%
Biochemistry, Genetics and Molecular Biology 1 2%
Other 2 4%
Unknown 7 15%