Hosted by: Division of Neurodegenerative Disorders, St. Boniface Hospital Research

Everyone Invited - DND Visiting Speaker - Dr. Sheena Josselyn

view online: http://www.sbrc.ca/2012/09/dnd-visiting-speaker-dr-sheena-josselyn-2/

Date: Friday, October 19, 2012 Time: 12:00 noon Location: Theatre C, Banantyne Campus

TOPIC: Making and Breaking Memories

http://www.sbrc.ca/wp-content/uploads/2012/05/josselyn.jpg Dr. Sheena Josselyn http://www.sickkids.ca/AboutSickKids/Directory/People/J/Sheena-Josselyn .html Senior Scientist, Neurosciences & Mental Health Canada Research Chair http://www.chairs.gc.ca/ , Molecular and Cellular Cognition Associate Professor, Department of Physiology University of Toronto Hospital for Sick Children, Toronto, ON

A fundamental goal of neuroscience is to understand how memories are encoded and stored in the brain. Indeed, identifying the physical basis of memory within the brain (the memory trace) has been a long-standing challenge for scientists since Karl Lashley's "search for the engram" in the 1950's. Memories are thought to be encoded by sparsely distributed groups of neurons. However, identifying the precise neurons supporting a given memory (the memory trace) has been a long-standing challenge. We have shown previously that lateral amygdala (LA) neurons with increased CREB are preferentially activated by fear memory expression, suggesting they are selectively recruited into the memory trace. Here we used an inducible diphtheria-toxin strategy to specifically ablate these neurons. Selectively deleting neurons overexpressing CREB (but not a similar portion of random LA neurons) after learning blocked expression of that fear memory. The resulting memory loss was robust and persistent, suggesting that the memory was permanently erased. These results establish a causal link between a specific neuronal subpopulation and memory expression, thereby identifying critical neurons within the memory trace.

Short bio: The research in Dr. Josselyn's lab is dedicated to understanding the neural basis of cognitive function and dysfunction. To unravel the molecular, cellular and circuit processes that underlie learning and memory, her lab uses a multidisciplinary approach include the use of genetically-engineered mice, viral vectors, cellular imaging, electrophysiology and detailed behavioral analysis. Her program of research focuses on two main elements 1) examining the brain regions and molecules responsible for normal memory formation and 2) using this knowledge to intervene in conditions in which memory is impaired (for instance in neurodegenerative diseases such as Alzheimer's disease). She has published extensively in the top scientific journals on these subjects and has shown that fear memories in mice can be "erased" and is currently examining novel treatments for the memory disorders that characterize Alzheimer's disease.

For more information, please contact the DND Office at :

t. 204.235.3939 e: dnd@sbrc.ca

Kelly Jorundson Winnipeg Chapter Society for Neuroscience R4046 - 351 Tache Avenue Winnipeg, MB R2H 2A6

Tel: 204.235.3939 Fax: 204.237.4092 Email: kjorund@sbrc.ca OR kjorund@yahoo.ca