Young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks

Adult neurogenesis supports performance in many hippocampal dependent tasks. Considering the small number of adult-born neurons generated at any given time, it is surprising that this sparse population of cells can substantially influence behavior. Recent studies have demonstrated that heightened ex...

全面介绍

书目详细资料
Main Authors: Zhuo, Jia-Min, Tseng, Hua-an, Desai, Mitul, Bucklin, Mark E, Mohammed, Ali I, Robinson, Nick TM, Rangel, Lara M, Jasanoff, Alan P, Gritton, Howard J, Han, Xue, Boyden, Edward
其他作者: Massachusetts Institute of Technology. Media Laboratory
格式: 文件
语言:en_US
出版: eLife Sciences Publications, Ltd. 2017
在线阅读:http://hdl.handle.net/1721.1/107997
https://orcid.org/0000-0002-0419-3351
_version_ 1826216461559922688
author Zhuo, Jia-Min
Tseng, Hua-an
Desai, Mitul
Bucklin, Mark E
Mohammed, Ali I
Robinson, Nick TM
Rangel, Lara M
Jasanoff, Alan P
Gritton, Howard J
Han, Xue
Boyden, Edward
author2 Massachusetts Institute of Technology. Media Laboratory
author_facet Massachusetts Institute of Technology. Media Laboratory
Zhuo, Jia-Min
Tseng, Hua-an
Desai, Mitul
Bucklin, Mark E
Mohammed, Ali I
Robinson, Nick TM
Rangel, Lara M
Jasanoff, Alan P
Gritton, Howard J
Han, Xue
Boyden, Edward
author_sort Zhuo, Jia-Min
collection MIT
description Adult neurogenesis supports performance in many hippocampal dependent tasks. Considering the small number of adult-born neurons generated at any given time, it is surprising that this sparse population of cells can substantially influence behavior. Recent studies have demonstrated that heightened excitability and plasticity may be critical for the contribution of young adult-born cells for certain tasks. What is not well understood is how these unique biophysical and synaptic properties may translate to networks that support behavioral function. Here we employed a location discrimination task in mice while using optogenetics to transiently silence adult-born neurons at different ages. We discovered that adult-born neurons promote location discrimination during early stages of development but only if they undergo maturation during task acquisition. Silencing of young adult-born neurons also produced changes extending to the contralateral hippocampus, detectable by both electrophysiology and fMRI measurements, suggesting young neurons may modulate location discrimination through influences on bilateral hippocampal networks.
first_indexed 2024-09-23T16:48:04Z
format Article
id mit-1721.1/107997
institution Massachusetts Institute of Technology
language en_US
last_indexed 2024-09-23T16:48:04Z
publishDate 2017
publisher eLife Sciences Publications, Ltd.
record_format dspace
spelling mit-1721.1/1079972022-10-03T08:24:49Z Young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks Zhuo, Jia-Min Tseng, Hua-an Desai, Mitul Bucklin, Mark E Mohammed, Ali I Robinson, Nick TM Rangel, Lara M Jasanoff, Alan P Gritton, Howard J Han, Xue Boyden, Edward Massachusetts Institute of Technology. Media Laboratory Boyden, Edward Adult neurogenesis supports performance in many hippocampal dependent tasks. Considering the small number of adult-born neurons generated at any given time, it is surprising that this sparse population of cells can substantially influence behavior. Recent studies have demonstrated that heightened excitability and plasticity may be critical for the contribution of young adult-born cells for certain tasks. What is not well understood is how these unique biophysical and synaptic properties may translate to networks that support behavioral function. Here we employed a location discrimination task in mice while using optogenetics to transiently silence adult-born neurons at different ages. We discovered that adult-born neurons promote location discrimination during early stages of development but only if they undergo maturation during task acquisition. Silencing of young adult-born neurons also produced changes extending to the contralateral hippocampus, detectable by both electrophysiology and fMRI measurements, suggesting young neurons may modulate location discrimination through influences on bilateral hippocampal networks. United States. National Institutes of Health (1DP2NS082126) National Institute of Mental Health (U.S.) (5R00MH085944) United States. National Institutes of Health (R01-DA028299) United States. Defense Advanced Research Projects Agency (W911NF-10-0059) Pew Charitable Trusts American Federation for Aging Research Alfred P. Sloan Foundation National Institute of Mental Health (U.S.) (1R21MH109941) 2017-04-10T14:07:21Z 2017-04-10T14:07:21Z 2016-12 2016-10 Article http://purl.org/eprint/type/JournalArticle 2050-084X http://hdl.handle.net/1721.1/107997 Zhuo, Jia-Min, Hua-an Tseng, Mitul Desai, Mark E Bucklin, Ali I Mohammed, Nick TM Robinson, Edward S Boyden, et al. “Young Adult Born Neurons Enhance Hippocampal Dependent Performance via Influences on Bilateral Networks.” eLife 5 (December 3, 2016). © 2016 eLife Sciences Publications Ltd. https://orcid.org/0000-0002-0419-3351 en_US http://dx.doi.org/10.7554/eLife.22429 eLife Creative Commons Attribution 4.0 International License http://creativecommons.org/licenses/by/4.0/ application/pdf eLife Sciences Publications, Ltd. eLife
spellingShingle Zhuo, Jia-Min
Tseng, Hua-an
Desai, Mitul
Bucklin, Mark E
Mohammed, Ali I
Robinson, Nick TM
Rangel, Lara M
Jasanoff, Alan P
Gritton, Howard J
Han, Xue
Boyden, Edward
Young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks
title Young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks
title_full Young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks
title_fullStr Young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks
title_full_unstemmed Young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks
title_short Young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks
title_sort young adult born neurons enhance hippocampal dependent performance via influences on bilateral networks
url http://hdl.handle.net/1721.1/107997
https://orcid.org/0000-0002-0419-3351
work_keys_str_mv AT zhuojiamin youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT tsenghuaan youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT desaimitul youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT bucklinmarke youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT mohammedalii youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT robinsonnicktm youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT rangellaram youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT jasanoffalanp youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT grittonhowardj youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT hanxue youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks
AT boydenedward youngadultbornneuronsenhancehippocampaldependentperformanceviainfluencesonbilateralnetworks