Cargando…

Real-time visualization of mRNA synthesis during memory formation in live mice

Memories are thought to be encoded in populations of neurons called memory trace or engram cells. However, little is known about the dynamics of these cells because of the difficulty in real-time monitoring of them over long periods of time in vivo. To overcome this limitation, we present a genetica...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Byung Hun, Shim, Jae Youn, Moon, Hyungseok C., Kim, Dong Wook, Kim, Jiwon, Yook, Jang Soo, Kim, Jinhyun, Park, Hye Yoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271212/
https://www.ncbi.nlm.nih.gov/pubmed/35776545
http://dx.doi.org/10.1073/pnas.2117076119
_version_ 1784744631657824256
author Lee, Byung Hun
Shim, Jae Youn
Moon, Hyungseok C.
Kim, Dong Wook
Kim, Jiwon
Yook, Jang Soo
Kim, Jinhyun
Park, Hye Yoon
author_facet Lee, Byung Hun
Shim, Jae Youn
Moon, Hyungseok C.
Kim, Dong Wook
Kim, Jiwon
Yook, Jang Soo
Kim, Jinhyun
Park, Hye Yoon
author_sort Lee, Byung Hun
collection PubMed
description Memories are thought to be encoded in populations of neurons called memory trace or engram cells. However, little is known about the dynamics of these cells because of the difficulty in real-time monitoring of them over long periods of time in vivo. To overcome this limitation, we present a genetically encoded RNA indicator (GERI) mouse for intravital chronic imaging of endogenous Arc messenger RNA (mRNA)—a popular marker for memory trace cells. We used our GERI to identify Arc-positive neurons in real time without the delay associated with reporter protein expression in conventional approaches. We found that the Arc-positive neuronal populations rapidly turned over within 2 d in the hippocampal CA1 region, whereas ∼4% of neurons in the retrosplenial cortex consistently expressed Arc following contextual fear conditioning and repeated memory retrievals. Dual imaging of GERI and a calcium indicator in CA1 of mice navigating a virtual reality environment revealed that only the population of neurons expressing Arc during both encoding and retrieval exhibited relatively high calcium activity in a context-specific manner. This in vivo RNA-imaging approach opens the possibility of unraveling the dynamics of the neuronal population underlying various learning and memory processes.
format Online
Article
Text
id pubmed-9271212
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-92712122022-07-11 Real-time visualization of mRNA synthesis during memory formation in live mice Lee, Byung Hun Shim, Jae Youn Moon, Hyungseok C. Kim, Dong Wook Kim, Jiwon Yook, Jang Soo Kim, Jinhyun Park, Hye Yoon Proc Natl Acad Sci U S A Biological Sciences Memories are thought to be encoded in populations of neurons called memory trace or engram cells. However, little is known about the dynamics of these cells because of the difficulty in real-time monitoring of them over long periods of time in vivo. To overcome this limitation, we present a genetically encoded RNA indicator (GERI) mouse for intravital chronic imaging of endogenous Arc messenger RNA (mRNA)—a popular marker for memory trace cells. We used our GERI to identify Arc-positive neurons in real time without the delay associated with reporter protein expression in conventional approaches. We found that the Arc-positive neuronal populations rapidly turned over within 2 d in the hippocampal CA1 region, whereas ∼4% of neurons in the retrosplenial cortex consistently expressed Arc following contextual fear conditioning and repeated memory retrievals. Dual imaging of GERI and a calcium indicator in CA1 of mice navigating a virtual reality environment revealed that only the population of neurons expressing Arc during both encoding and retrieval exhibited relatively high calcium activity in a context-specific manner. This in vivo RNA-imaging approach opens the possibility of unraveling the dynamics of the neuronal population underlying various learning and memory processes. National Academy of Sciences 2022-07-01 2022-07-05 /pmc/articles/PMC9271212/ /pubmed/35776545 http://dx.doi.org/10.1073/pnas.2117076119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Lee, Byung Hun
Shim, Jae Youn
Moon, Hyungseok C.
Kim, Dong Wook
Kim, Jiwon
Yook, Jang Soo
Kim, Jinhyun
Park, Hye Yoon
Real-time visualization of mRNA synthesis during memory formation in live mice
title Real-time visualization of mRNA synthesis during memory formation in live mice
title_full Real-time visualization of mRNA synthesis during memory formation in live mice
title_fullStr Real-time visualization of mRNA synthesis during memory formation in live mice
title_full_unstemmed Real-time visualization of mRNA synthesis during memory formation in live mice
title_short Real-time visualization of mRNA synthesis during memory formation in live mice
title_sort real-time visualization of mrna synthesis during memory formation in live mice
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271212/
https://www.ncbi.nlm.nih.gov/pubmed/35776545
http://dx.doi.org/10.1073/pnas.2117076119
work_keys_str_mv AT leebyunghun realtimevisualizationofmrnasynthesisduringmemoryformationinlivemice
AT shimjaeyoun realtimevisualizationofmrnasynthesisduringmemoryformationinlivemice
AT moonhyungseokc realtimevisualizationofmrnasynthesisduringmemoryformationinlivemice
AT kimdongwook realtimevisualizationofmrnasynthesisduringmemoryformationinlivemice
AT kimjiwon realtimevisualizationofmrnasynthesisduringmemoryformationinlivemice
AT yookjangsoo realtimevisualizationofmrnasynthesisduringmemoryformationinlivemice
AT kimjinhyun realtimevisualizationofmrnasynthesisduringmemoryformationinlivemice
AT parkhyeyoon realtimevisualizationofmrnasynthesisduringmemoryformationinlivemice