Improved Specificity of Hippocampal Memory Trace Labeling

被引:34
作者
Cazzulino, Alejandro S. [1 ,2 ]
Martinez, Randy [3 ]
Tomm, Nicole K. [1 ,2 ,4 ]
Denny, Christine A. [1 ,2 ]
机构
[1] Columbia Univ, Dept Psychiat, New York, NY USA
[2] New York State Psychiat Inst & Hosp, Div Integrat Neurosci, Res Fdn Mental Hyg Inc RFMH, New York, NY 10032 USA
[3] Columbia Univ BRAINYAC, Brain Res Apprenticeships New York, New York, NY USA
[4] Univ Minnesota, Sch Med, Duluth, MN 55812 USA
关键词
Hippocampus; c-fos; Arc; learning; memory; IMMEDIATE-EARLY GENE; REGULATED GENE; FEAR MEMORY; EXPRESSION; TAMOXIFEN; RECOMBINATION; NEUROGENESIS; ARC;
D O I
10.1002/hipo.22556
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent studies have focused on the identification and manipulation of memory traces in rodent models. The two main mouse models utilized are either a CreER(T2)/loxP tamoxifen (TAM)-or a tetracycline transactivator/tetracycline-response element doxycycline-inducible system. These systems, however, could be improved to label a more specific population of activated neurons corresponding to behavior. Here, we sought to identify an improved selective estrogen receptor (ER) modulator (SERM) in which we could label an individual memory trace in ArcCreER(T2) mice. We found that 4-hydroxytamoxifen (4-OHT) is a selective SERM in the ArcCreER(T2) 3 Rosa26-CAG-stop(flox)-channelrhodospin (ChR2)-enhanced yellow fluorescent protein (eYFP) mice. The half-life of 4-OHT is shorter than TAM, allowing for more specificity of memory trace labeling. Furthermore, 4-OHT allowed for context-specific labeling in the dentate gyrus and CA3. In summary, we believe that 4-OHT improves the specificity of memory trace labeling and will allow for refined memory trace studies in the future. (C) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:752 / 762
页数:11
相关论文
共 26 条
[1]   Structural and molecular interrogation of intact biological systems [J].
Chung, Kwanghun ;
Wallace, Jenelle ;
Kim, Sung-Yon ;
Kalyanasundaram, Sandhiya ;
Andalman, Aaron S. ;
Davidson, Thomas J. ;
Mirzabekov, Julie J. ;
Zalocusky, Kelly A. ;
Mattis, Joanna ;
Denisin, Aleksandra K. ;
Pak, Sally ;
Bernstein, Hannah ;
Ramakrishnan, Charu ;
Grosenick, Logan ;
Gradinaru, Viviana ;
Deisseroth, Karl .
NATURE, 2013, 497 (7449) :332-+
[2]   Selection of distinct populations of dentate granule cells in response to inputs as a mechanism for pattern separation in mice [J].
Deng, Wei ;
Mayford, Mark ;
Gage, Fred H. .
ELIFE, 2013, 2
[3]   Hippocampal Memory Traces Are Differentially Modulated by Experience, Time, and Adult Neurogenesis [J].
Denny, Christine A. ;
Kheirbek, Mazen A. ;
Alba, Eva L. ;
Tanaka, Kenji F. ;
Brachman, Rebecca A. ;
Laughman, Kimberly B. ;
Tomm, Nicole K. ;
Turi, Gergely F. ;
Losonczy, Attila ;
Hen, Rene .
NEURON, 2014, 83 (01) :189-201
[4]   4-to 6-week-old adult-born hippocampal neurons influence novelty-evoked exploration and contextual fear conditioning [J].
Denny, Christine A. ;
Burghardt, Nesha S. ;
Schachter, Daniel M. ;
Hen, Rene ;
Drew, Michael R. .
HIPPOCAMPUS, 2012, 22 (05) :1188-1201
[5]   Arrest of Adult Hippocampal Neurogenesis in Mice Impairs Single- But Not Multiple-Trial Contextual Fear Conditioning [J].
Drew, Michael R. ;
Denny, Christine A. ;
Hen, Rene .
BEHAVIORAL NEUROSCIENCE, 2010, 124 (04) :446-454
[6]   Permanent Genetic Access to Transiently Active Neurons via TRAP: Targeted Recombination in Active Populations [J].
Guenthner, Casey J. ;
Miyamichi, Kazunari ;
Yang, Helen H. ;
Heller, H. Craig ;
Luo, Liqun .
NEURON, 2013, 78 (05) :773-784
[7]   Environment-specific expression of the immediate-early gene Arc in hippocampal neuronal ensembles [J].
Guzowski, JF ;
McNaughton, BL ;
Barnes, CA ;
Worley, PF .
NATURE NEUROSCIENCE, 1999, 2 (12) :1120-1124
[8]   Selective Erasure of a Fear Memory [J].
Han, Jin-Hee ;
Kushner, Steven A. ;
Yiu, Adelaide P. ;
Hsiang, Hwa-Lin ;
Buch, Thorsten ;
Waisman, Ari ;
Bontempi, Bruno ;
Neve, Rachael L. ;
Frankland, Paul W. ;
Josselyn, Sheena A. .
SCIENCE, 2009, 323 (5920) :1492-1496
[9]   Efficient recombination in diverse tissues by a tamoxifen-inducible form of Cre: A tool for temporally regulated gene activation/inactivation in the mouse [J].
Hayashi, S ;
McMahon, AP .
DEVELOPMENTAL BIOLOGY, 2002, 244 (02) :305-318
[10]   Continuing the search for the engram: examining the mechanism of fear memories [J].
Josselyn, Sheena A. .
JOURNAL OF PSYCHIATRY & NEUROSCIENCE, 2010, 35 (04) :221-228