Computing with microtubules (Craddock, Tuszynski, Hameroff 2012)

This paper hypothesizes that postsynaptic CaMKII (calcium/calmodulin-dependent protein kinase II) receives synaptic input and then interacts with via phosphorylation, suggesting that memories may be encoded in the microtubules in this way. They note that the size and shape of CaMKII appears to be just right to phosphorylate the hexagonal lattices of tubulin proteins in microtubules. The paper also can “demonstrate microtubule-associated protein logic gates, and show how patterns of phosphorylated tubulins in microtubules can control neuronal functions by triggering axonal firings, regulating synapses, and traversing scale.”. Via ScienceDaily.

Travis J. A. Craddock, Jack A. Tuszynski, Stuart Hameroff. Cytoskeletal Signaling: Is Memory Encoded in Microtubule Lattices by CaMKII Phosphorylation? PLoS Computational Biology, 2012; 8 (3): e1002421 DOI: 10.1371/journal.pcbi.1002421.

Neuroscience as a new national priority

President Obama: “Now, it’s time to get to work.”

NYT article:

Single neurons can distinguish inward temporal sequences from outward

“activating synapses in a centrifugal sequence (outward from the soma) caused a different [lesser] [cortical pyramidal] neuronal response than activating the synapses in a centripetal (inward) sequence”

Alain Destexhe. Dendrites Do It in Sequences (24 September 2010)
Science 329 (5999), 1611.


Tiago Branco, Beverley A. Clark, and Michael Häusser. Dendritic Discrimination of Temporal Input Sequences in Cortical Neurons (24 September 2010)
Science 329 (5999), 1671.

Dendritic organization of sensory input to cortical neurons in vivo

Jia, H., Rochefort, N., Chen, X., & Konnerth, A. (2010). Dendritic organization of sensory input to cortical neurons in vivo Nature, 464 (7293), 1307-1312 DOI: 10.1038/nature08947

Consider a a cortical neuron in V1, layer 2/3, whose output shows sharp orientation tuning. What are the orientation tunings of the most important inputs to that neuron? What is the spatial distribution of these inputs in the neuron’s dendritic tree?

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Genetic tagging of the particular neurons in the basolateral amygdala that store a particular engram

When we learn new information we use only a tiny fraction of the neurons in our brain for that particular memory trace. In order to allow the molecular study of those specific neurons we combined elements of the tet system with a promoter that is activated by high level neural activity (the cfos promoter) to generate mice in which a genetic tag can be introduced into neurons that are active at a given point in time. The tag can be maintained for a prolonged period, creating a precise record of the neural activity pattern at a specific point in time. Using fear conditioning we found that the same neurons activated during learning were reactivated when the animal recalled the fearful event. We also found that these neurons were no longer activated following memory extinction, consistent with the idea that extinction modifies a component of the original memory trace.

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