* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Actin , Synaptic plasticity in Parallel fibre-Purkinje Neuron
Nervous system network models wikipedia , lookup
NMDA receptor wikipedia , lookup
Memory consolidation wikipedia , lookup
Biological neuron model wikipedia , lookup
Environmental enrichment wikipedia , lookup
Haemodynamic response wikipedia , lookup
Subventricular zone wikipedia , lookup
Apical dendrite wikipedia , lookup
Neurotransmitter wikipedia , lookup
Optogenetics wikipedia , lookup
Neuropsychopharmacology wikipedia , lookup
Holonomic brain theory wikipedia , lookup
Development of the nervous system wikipedia , lookup
Neuromuscular junction wikipedia , lookup
Feature detection (nervous system) wikipedia , lookup
Pre-Bötzinger complex wikipedia , lookup
Synaptic noise wikipedia , lookup
Molecular neuroscience wikipedia , lookup
De novo protein synthesis theory of memory formation wikipedia , lookup
Long-term potentiation wikipedia , lookup
Neuroanatomy wikipedia , lookup
Clinical neurochemistry wikipedia , lookup
Metastability in the brain wikipedia , lookup
Synaptic gating wikipedia , lookup
Eyeblink conditioning wikipedia , lookup
Channelrhodopsin wikipedia , lookup
Neuroplasticity wikipedia , lookup
Dendritic spine wikipedia , lookup
Chemical synapse wikipedia , lookup
Long-term depression wikipedia , lookup
Synaptogenesis wikipedia , lookup
Role of Actin on Synaptic plasticity in Parallel fibre - Purkinje Neuron Synapse of Cerebellum Dharmarajgireesh.E Supervisors: Dr. Karuhiko Yamaguchi, BSI, RIKEN Prof. S. Maka, Dept. of Electrical Engineering, IIT Kharagpur Laboratory: Laboratory of Memory and Learning, Brain Science Institute, RIKEN, Japan Abstract The neuronal plasticity induced by long term depression (LTD) in parallel fibre Purkinje cell synapse has been known to be one of the important mechanisms of motor learning. The molecular mechanisms behind this plasticity are being elucidated at various levels. Cytoskeleton is speculated to have a major role in consolidating synaptic plasticity. To analyse the role of actin in induction and maintenance of synaptic plasticity pharmacological agents causing both actin depolymerisation and stabilisation were injected intracellularly in Purkinje cells. Latrunculin A, a f-actin depolymerising agent enhanced the rate and depth of long term depression induced by conjuncive stimulation effected by depolarising Purkinje cells and stimulating Parallel fibres simultaneously. Jasplakinolide, an actin stabilizing agent blocked the induction of LTD by the same protocol. The possiblility that actin depolymerisation as such may be affecting calcium channel activity and thereby modulating the depth of LTD was investigated by recording Calcium current from cells injected with Latrunculin . It was observed that the Calcium current amplitude is decreasing after Latrunculin injection over a time period. This has been reported in many other cells even though not well documented in neurons. To study the possibility of the variations in the morphology due to altered stability of actin cytoskeleton affecting neuronal plasticity, Luciferase yellow was injected along with Latrunculin and the dendritic spines were observed. It was noted that there was no significant change in the morphology of dendritic spines in the given concentration of Latrunculin even after 30 minutes. The role of actin in another kind of synaptic plasticity – Long term potentiation (LTP) taking place between parallel fibre and Purkinje neuron- was explored. Preliminary studies indicated that actin depolymerising drug can block the induction of LTP. The studies undertaken are strongly suggestive that actin filament dynamics has a dominant role to play in the synaptic plasticity between parallel fibres and Purkinje neurons. This finding is in consonance with similar findings in Hippocampus and other parts of brain. The most plausible mechanism of action of f-actin dynamics on synaptic plasticity could be through its effect on AMPA clustering and declustering. This becomes the most likely mechanism because other possibilities like 1. effect on transportation, 2. effect on dendritic morphology and 3. effect on Calcium dynamics, were ruled out in the experiments done.