terça-feira, 24 de fevereiro de 2009

Brain Plasticity during Learning and Memory

Caltech Today Streaming Theater

By Erin M. Schuman

Synapses, the points of contact and communication between neurons, can vary in their size, strength and number. These differences in synapses and their ability to change throughout the lifetime of the animal contributes to our ability to learn and remember. We are interested in how synapses are modified at the cellular and molecular level. We are also interested in how neuronal circuits change when synapses change their properties. We conduct all of our studies in the hippocampus, a structure known to be important for memory in both humans and animals. We use molecular biology, electrophysiology and imaging to address the questions detailed below. A major focus of the lab concerns the cell biological mechanisms that govern modifications at individual synaptic sites. In particular, we are interested in the idea that dendritic protein synthesis and degradation may contribute to synaptic plasticity. We are also interested in mRNA and protein trafficking during synaptic plasticity. We are also examining the role of the cadherins family of cell adhesion molecules in synaptic plasticity. Several labs have shown that cadherins are localized to synapses in the hippocampus. Earlier, we demonstrated that function-blocking cadherin antibodies or peptides can prevent long-term potentiation, without interfering with basal synaptic transmission. We hypothesize that cadherin bonds may be sensitive to local fluxes in extracellular calcium imposed by action potential activity. We are now examining the molecular mechanisms by which cadherins influence synaptic strength and the involvement of cadherins in the formation and maintenance of synapses, using fluorescence resonance energy transfer and endocytosis assays.