ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

Active dendrites regulate the spatiotemporal spread of signaling microdomains

Basak, Reshma and Narayanan, Rishikesh (2018) Active dendrites regulate the spatiotemporal spread of signaling microdomains. In: PLOS COMPUTATIONAL BIOLOGY, 14 (11).

[img] PDF
Plo_Com_Bio_14-11_2018.pdf.crdownload - Published Version

Download (4MB)
Official URL: https://doi.org/10.1371/journal.pcbi.1006485


Microdomains that emerge from spatially constricted spread of biochemical signaling components play a central role in several neuronal computations. Although dendrites, endowed with several voltage-gated ion channels, form a prominent structural substrate for microdomain physiology, it is not known if these channels regulate the spatiotemporal spread of signaling microdomains. Here, we employed a multiscale, morphologically realistic, conductance-based model of the hippocampal pyramidal neuron that accounted for experimental details of electrical and calcium-dependent biochemical signaling. We activated synaptic N-Methyl-D-Aspartate receptors through theta-burst stimulation (TBS) or pairing (TBP) and assessed microdomain propagation along a signaling pathway that included calmodulin, calcium/calmodulin-dependent protein kinase II (CaMKII) and protein phosphatase 1. We found that the spatiotemporal spread of the TBS-evoked microdomain in phosphorylated CaMKII (pCaMKII) was amplified in comparison to that of the corresponding calcium microdomain. Next, we assessed the role of two dendritically expressed inactivating channels, one restorative (A-type potassium) and another regenerative (T-type calcium), by systematically varying their conductances. Whereas A-type potassium channels suppressed the spread of pCaMKII microdomains by altering the voltage response to TBS, T-type calcium channels enhanced this spread by modulating TBS-induced calcium influx without changing the voltage. Finally, we explored cross-dependencies of these channels with other model components, and demonstrated the heavy mutual interdependence of several biophysical and biochemical properties in regulating microdomains and their spread. Our conclusions unveil a pivotal role for dendritic voltage-gated ion channels in actively amplifying or suppressing biochemical signals and their spatiotemporal spread, with critical implications for clustered synaptic plasticity, robust information transfer and efficient neural coding.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to PUBLIC LIBRARY SCIENCE
Department/Centre: Division of Biological Sciences > Molecular Biophysics Unit
Date Deposited: 24 Jan 2019 09:59
Last Modified: 24 Jan 2019 09:59
URI: http://eprints.iisc.ac.in/id/eprint/61399

Actions (login required)

View Item View Item