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Npas4 Is a Critical Regulator of Learning-Induced Plasticity at Mossy Fiber-CA3 Synapses during Contextual Memory Formation

Authors :
McGovern Institute for Brain Research at MIT
Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
Picower Institute for Learning and Memory
Massachusetts Institute of Technology. Institute for Medical Engineering & Science
Massachusetts Institute of Technology. Department of Chemical Engineering
Harvard University--MIT Division of Health Sciences and Technology
Weng, Feng-Ju
Garcia, Rodrigo
Lutzu, Stefano
Alviña, Karina
Zhang, Yuxiang
Dushko, Margaret
Ku, Taeyun
Zemoura, Khaled
Rich, David
Garcia-Dominguez, Dario
Hung, Matthew
Yelhekar, Tushar D
Sørensen, Andreas Toft
Xu, Weifeng
Chung, Kwanghun
Castillo, Pablo E.
Lin, Yingxi
McGovern Institute for Brain Research at MIT
Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
Picower Institute for Learning and Memory
Massachusetts Institute of Technology. Institute for Medical Engineering & Science
Massachusetts Institute of Technology. Department of Chemical Engineering
Harvard University--MIT Division of Health Sciences and Technology
Weng, Feng-Ju
Garcia, Rodrigo
Lutzu, Stefano
Alviña, Karina
Zhang, Yuxiang
Dushko, Margaret
Ku, Taeyun
Zemoura, Khaled
Rich, David
Garcia-Dominguez, Dario
Hung, Matthew
Yelhekar, Tushar D
Sørensen, Andreas Toft
Xu, Weifeng
Chung, Kwanghun
Castillo, Pablo E.
Lin, Yingxi
Source :
PMC
Publication Year :
2020

Abstract

Synaptic connections between hippocampal mossy fibers (MFs) and CA3 pyramidal neurons are essential for contextual memory encoding, but the molecular mechanisms regulating MF-CA3 synapses during memory formation and the exact nature of this regulation are poorly understood. Here we report that the activity-dependent transcription factor Npas4 selectively regulates the structure and strength of MF-CA3 synapses by restricting the number of their functional synaptic contacts without affecting the other synaptic inputs onto CA3 pyramidal neurons. Using an activity-dependent reporter, we identified CA3 pyramidal cells that were activated by contextual learning and found that MF inputs on these cells were selectively strengthened. Deletion of Npas4 prevented both contextual memory formation and this learning-induced synaptic modification. We further show that Npas4 regulates MF-CA3 synapses by controlling the expression of the polo-like kinase Plk2. Thus, Npas4 is a critical regulator of experience-dependent, structural, and functional plasticity at MF-CA3 synapses during contextual memory formation. Weng et al. report that the transcription factor Npas4 selectively regulates the number of functional synaptic contacts between CA3 pyramidal neurons and mossy fibers, allowing for learning-induced modification of MF-CA3 synapses during contextual memory formation.<br />NIH (Grants DA017392, NS090473, MH081935, MH091220, NS088421, and DC014701)

Details

Database :
OAIster
Journal :
PMC
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1239995959
Document Type :
Electronic Resource