Cognitive resilience is mediated by the MEF2 network in mice and humans

Thesis: Ph. D., Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, February, 2021

Bibliographic Details
Main Author: Barker, Scarlett J.V.(Scarlett Jazmine)
Other Authors: Li-Huei Tsai.
Format: Thesis
Language:eng
Published: Massachusetts Institute of Technology 2021
Subjects:
Online Access:https://hdl.handle.net/1721.1/130809
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author Barker, Scarlett J.V.(Scarlett Jazmine)
author2 Li-Huei Tsai.
author_facet Li-Huei Tsai.
Barker, Scarlett J.V.(Scarlett Jazmine)
author_sort Barker, Scarlett J.V.(Scarlett Jazmine)
collection MIT
description Thesis: Ph. D., Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, February, 2021
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spelling mit-1721.1/1308092021-05-26T03:01:42Z Cognitive resilience is mediated by the MEF2 network in mice and humans Barker, Scarlett J.V.(Scarlett Jazmine) Li-Huei Tsai. Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences. Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences Brain and Cognitive Sciences. Thesis: Ph. D., Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences, February, 2021 Cataloged from the official PDF version of thesis. "February 2021." Includes bibliographical references (pages 119-126). Recent increases in human longevity have been accompanied by a rise in the incidence of dementia. While a large proportion of aged individuals display pathological hallmarks of neurodegenerative disease, a small number of these individuals are able to maintain healthy cognitive function even in the presence of extensive brain pathology. The molecular mechanisms that govern this neuro-protected state remain unknown, but individuals that exhibit cognitive resilience (CgR) represent a unique source of insight into potential therapies that could preserve brain function in the face of neurodegenerative disease. Here, we employ a two-pronged approach to dissect the mechanism underlying CgR. First, using multiple integrated repositories of clinical and brain transcriptomic data we identified individuals who maintained normal cognition despite harboring a large burden of Alzheimer's disease (AD) pathology. We observe significant up-regulation of MEF2 family members in these resilient patients when compared to patients whose cognition declined in the presence of pathology. Second, we utilize the only existing animal model of CgR -- environmental enrichment -- to investigate the molecular mechanisms involved in the induction of resilience. Accessibility of Mef2 binding sites, and expression of Mef2 targets are significantly increased upon enrichment. Additionally, knockdown of Mef2 family members just prior to the initiation of enrichment block its cognitive benefits, demonstrating the necessity of Mef2 activity for achieving the enhanced cognitive potential afforded by enrichment. Neurons lacking Mef2 are hyperexcitable, which is also one of the earliest pathological alterations observed in AD. These results suggest a potential mechanistic link between the Mef2 transcriptional network induced by enrichment and the prevention of disease-associated hyperexcitability. To determine the causal impact of Mef2 on cognition in the context of neurodegeneration, we use a viral approach to manipulate the PS19 mouse model of tauopathy. Remarkably, in the absence of enrichment, Mef2 overexpression alone is sufficient to improve cognition and reduce hyperexcitability in PS19 mice. Overall, our findings reveal a novel role for MEF2 transcription factors in promoting cognition throughout life, and maintaining cognitive resilience in the context of neurodegenerative disease. by Scarlett J.V. Barker. Ph. D. Ph.D. Massachusetts Institute of Technology, Department of Brain and Cognitive Sciences 2021-05-25T18:20:49Z 2021-05-25T18:20:49Z 2021 2021 Thesis https://hdl.handle.net/1721.1/130809 1252627386 eng MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided. http://dspace.mit.edu/handle/1721.1/7582 126 pages application/pdf Massachusetts Institute of Technology
spellingShingle Brain and Cognitive Sciences.
Barker, Scarlett J.V.(Scarlett Jazmine)
Cognitive resilience is mediated by the MEF2 network in mice and humans
title Cognitive resilience is mediated by the MEF2 network in mice and humans
title_full Cognitive resilience is mediated by the MEF2 network in mice and humans
title_fullStr Cognitive resilience is mediated by the MEF2 network in mice and humans
title_full_unstemmed Cognitive resilience is mediated by the MEF2 network in mice and humans
title_short Cognitive resilience is mediated by the MEF2 network in mice and humans
title_sort cognitive resilience is mediated by the mef2 network in mice and humans
topic Brain and Cognitive Sciences.
url https://hdl.handle.net/1721.1/130809
work_keys_str_mv AT barkerscarlettjvscarlettjazmine cognitiveresilienceismediatedbythemef2networkinmiceandhumans