Neuroscientists Identify Fundamental Mechanism for Long Term Memory Storage

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A University of Iowa neuroscience research team has identified a fundamental biochemical mechanism underlying memory storage and has linked this mechanism to cognitive deficits in mouse models of Alzheimer’s Disease and Related Dementias.

While working to understand how memories are formed and stored in the brain, the team identified a novel protein folding mechanism in the endoplasmic reticulum that is essential for long term memory storage. They further demonstrated that this mechanism is impaired in a tau-based mouse model of Alzheimer’s disease and that restoring this protein folding mechanism reverses memory impairment in this mouse model for the study of dementia. The findings are published in the March 23 issue of the journal Science Advances.

Snehajyoti Chatterjee

Snehajyoti Chatterjee, PhD, co-first author of the study and a research associate in the lab of Ted Abel, PhD. Credit: University of Iowa

The team was led by Snehajyoti Chatterjee, PhD, a research associate in the lab of Ted Abel, PhD, Director of the Iowa Neuroscience Institute and chair and DEO of the UI Department of Neuroscience and Pharmacology. The Abel lab has previously shown that the Nr4a family of transcription factors is essential for long term memory consolidation. This study identified chaperone proteins in the endoplasmic reticulum, which are regulated by Nr4a.

“The role of protein folding machinery in long term memory has been overlooked for decades. We know that gene expression and protein synthesis are essential for long term memory consolidation and following learning a large number of proteins are synthesized. For proteins to be functionally active they need to be folded correctly. Our work demonstrates the conceptual idea that these chaperone proteins are the ones that actually fold the proteins to impact synaptic function and plasticity.”
Snehajyoti Chatterjee, PhD

The team also used gene therapy to reactivate the chaperone protein in a mouse model and found that the memory deficit was reversed, confirming that the protein folding machinery acts as a molecular switch for memory.

“Identifying this protein folding mechanism is a crucial step toward understanding how memories are stored and what goes wrong in diseases associated with memory impairment,” Abel says. “Even though we are not yet at a point of translating this to patient care, understanding this pathway is essential to one day being able to prevent and treat neurodegenerative disease.”

Reference: “Endoplasmic reticulum chaperone genes encode effectors of long-term memory” by Snehajyoti Chatterjee, Ethan Bahl, Utsav Mukherjee, Emily N. Walsh, Mahesh Shivarama Shetty, Amy L. Yan, Yann Vanrobaeys, Joseph D. Lederman, K. Peter Giese, Jacob Michaelson and Ted Abel, 23 March 2022, Science Advances.
DOI: 10.1126/sciadv.abm6063

In addition to Chatterjee and Abel, the research team included Jacob Michaelson, UI associate professor of psychiatry; postdoctoral scholar Mahesh Shivarama Shetty; graduate students Ethan Bahl, Utsav Mukherjee, Yann Vanrobaeys, and Emily N. Walsh; lab assistants Amy L. Yan and Joseph D. Lederman; and K. Peter Giese of Kings College, London.

The work was supported by NIH grant R01 MH087463, NIH grant K99 AG 068306, Nellie Ball Trust, The Gary & LaDonna Wicklund Research Fund for Cognitive Memory Disorders, The University of Iowa Hawkeye Intellectual and Developmental Disabilities Research Center, and the Roy J. Carver Charitable Trust.



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