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Beyond AMPA and NMDA: Slow synaptic mGlu/TRPC currents: Implications for dendritic integration
KTH, School of Computer Science and Communication (CSC), Computational Biology, CB. (Erik Fransén)
2010 (English)Licentiate thesis, comprehensive summary (Other academic)
Abstract [en]

In order to understand how the brain functions, under normal as well as pathological conditions, it is important to study the mechanisms underlying information integration. Depending on the nature of an input arriving at a synapse, different strategies may be used by the neuron to integrate and respond to the input. Naturally, if a short train of high-frequency synaptic input arrives, it may be beneficial for the neuron to be equipped with a fast mechanism that is highly sensitive to inputs on a short time scale. If, on the contrary, inputs arriving with low frequency are to be processed, it may be necessary for the neuron to possess slow mechanisms of integration. For example, in certain working memory tasks (e. g. delay-match-to-sample), sensory inputs may arrive separated by silent intervals in the range of seconds, and the subject should respond if the current input is identical to the preceeding input. It has been suggested that single neurons, due to intrinsic mechanisms outlasting the duration of input, may be able to perform such calculations. In this work, I have studied a mechanism thought to be particularly important in supporting the integration of low-frequency synaptic inputs. It is mediated by a cascade of events that starts with activation of group I metabotropic glutamate receptors (mGlu1/5), and ends with a membrane depolarization caused by a current that is mediated by canonical transient receptor potential (TRPC) ion channels. This current, denoted ITRPC, is the focus of this thesis.

A specific objective of this thesis is to study the role of ITRPC in the integration of synaptic inputs arriving at a low frequency, < 10 Hz. Our hypothesis is that, in contrast to the well-studied, rapidly decaying AMPA and NMDA currents, ITRPC is well-suited for supporting temporal summation of such synaptic input. The reason for choosing this range of frequencies is that neurons often communicate with signals (spikes) around 8 Hz, as shown by single-unit recordings in behaving animals. This is true for several regions of the brain, including the entorhinal cortex (EC) which is known to play a key role in producing working memory function and enabling long-term memory formation in the hippocampus.

Although there is strong evidence suggesting that ITRPC is important for neuronal communication, I have not encountered a systematic study of how this current contributes to synaptic integration. Since it is difficult to directly measure the electrical activity in dendritic branches using experimental techniques, I use computational modeling for this purpose. I implemented the components necessary for studying ITRPC, including a detailed model of extrasynaptic glutamate concentration, mGlu1/5 dynamics and the TRPC channel itself. I tuned the model to replicate electrophysiological in vitro data from pyramidal neurons of the rodent EC, provided by our experimental collaborator. Since we were interested in the role of ITRPC in temporal summation, a specific aim was to study how its decay time constant (τdecay) is affected by synaptic stimulus parameters.

The hypothesis described above is supported by our simulation results, as we show that synaptic inputs arriving at frequencies as low as 3 - 4 Hz can be effectively summed. We also show that τdecay increases with increasing stimulus duration and frequency, and that it is linearly dependent on the maximal glutamate concentration. Under some circumstances it was problematic to directly measure τdecay, and we then used a pair-pulse paradigm to get an indirect estimate of τdecay.

I am not aware of any computational model work taking into account the synaptically evoked ITRPC current, prior to the current study, and believe that it is the first of its kind. We suggest that ITRPC is important for slow synaptic integration, not only in the EC, but in several cortical and subcortical regions that contain mGlu1/5 and TRPC subunits, such as the prefrontal cortex. I will argue that this is further supported by studies using pharmacological blockers as well as studies on genetically modified animals.

Place, publisher, year, edition, pages
Stockholm: KTH , 2010. , viii, 67 p.
Trita-CSC-A, ISSN 1653-5723 ; 2010:13
Keyword [en]
transient receptor potential, TRP, metabotropic glutamate receptor, mGlu1/5, dendritic integration, synaptic activation, temporal summation, low-frequency, entorhinal cortex, mathematical model, computational neuroscience
National Category
Computer Science
URN: urn:nbn:se:kth:diva-24833ISBN: 978-91-7415-745-1OAI: diva2:353525
2010-10-29, RB35, Roslagstullsbacken 35, Stockholm, AlbaNova, 13:00
QC 20101005Available from: 2010-10-05 Created: 2010-09-27 Last updated: 2011-11-30Bibliographically approved
List of papers
1. Low-frequency summation of synaptically activated transient receptor potential channel-mediated depolarizations
Open this publication in new window or tab >>Low-frequency summation of synaptically activated transient receptor potential channel-mediated depolarizations
2011 (English)In: European Journal of Neuroscience, ISSN 0953-816X, E-ISSN 1460-9568, Vol. 34, no 4, 578-593 p.Article in journal (Refereed) Published
Abstract [en]

Neurons sum their input by spatial and temporal integration. Temporally, presynaptic firing rates are converted to dendritic membrane depolarizations by postsynaptic receptors and ion channels. In several regions of the brain, including higher association areas, the majority of firing rates are low. For rates below 20 Hz, the ionotropic receptors alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor and N-methyl-d-aspartate (NMDA) receptor will not produce effective temporal summation. We hypothesized that depolarization mediated by transient receptor potential (TRP) channels activated by metabotropic glutamate receptors would be more effective, owing to their slow kinetics. On the basis of voltage-clamp and current-clamp recordings from a rat slice preparation, we constructed a computational model of the TRP channel and its intracellular activation pathway, including the metabotropic glutamate receptor. We show that synaptic input frequencies down to 3-4 Hz and inputs consisting of as few as three to five pulses can be effectively summed. We further show that the time constant of integration increases with increasing stimulation frequency and duration. We suggest that the temporal summation characteristics of TRP channels may be important at distal dendritic arbors, where spatial summation is limited by the number of concurrently active synapses. It may be particularly important in regions characterized by low and irregular rates.

computational model, dendritic integration, entorhinal cortex, integration time constant, mGluR
National Category
Neurosciences Bioinformatics (Computational Biology)
urn:nbn:se:kth:diva-38955 (URN)10.1111/j.1460-9568.2011.07791.x (DOI)000293907400007 ()21777305 (PubMedID)2-s2.0-80051673126 (ScopusID)
Swedish Research Council, 621-2007-3774
Available from: 2011-09-06 Created: 2011-09-05 Last updated: 2012-09-14Bibliographically approved
2. TRPC channels activated by group 1 mG1uR in Entorhinal pyramidal neurons support integration of low frequency (<10 Hz) synaptic inputs
Open this publication in new window or tab >>TRPC channels activated by group 1 mG1uR in Entorhinal pyramidal neurons support integration of low frequency (<10 Hz) synaptic inputs
2009 (English)In: BMC Neuroscience, ISSN 1471-2202, Vol. 10, no Suppl 1, P26- p.Article in journal (Refereed) Published
National Category
Neurosciences Bioinformatics (Computational Biology)
urn:nbn:se:kth:diva-25000 (URN)10.1186/1471-2202-10-S1-P26 (DOI)
QC 20101005Available from: 2010-10-05 Created: 2010-10-05 Last updated: 2012-09-14Bibliographically approved

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