Author
Listed:
- Masanori Nomoto
(Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama
CREST, JST, University of Toyama)
- Noriaki Ohkawa
(Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama
CREST, JST, University of Toyama)
- Hirofumi Nishizono
(CREST, JST, University of Toyama
Life Science Research Center, University of Toyama)
- Jun Yokose
(Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama
CREST, JST, University of Toyama)
- Akinobu Suzuki
(Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama
CREST, JST, University of Toyama)
- Mina Matsuo
(Life Science Research Center, University of Toyama)
- Shuhei Tsujimura
(Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama
CREST, JST, University of Toyama)
- Yukari Takahashi
(Jikei University School of Medicine)
- Masashi Nagase
(Jikei University School of Medicine)
- Ayako M. Watabe
(Jikei University School of Medicine)
- Fusao Kato
(Jikei University School of Medicine)
- Kaoru Inokuchi
(Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama
CREST, JST, University of Toyama)
Abstract
Behavioural tagging is the transformation of a short-term memory, induced by a weak experience, into a long-term memory (LTM) due to the temporal association with a novel experience. The mechanism by which neuronal ensembles, each carrying a memory engram of one of the experiences, interact to achieve behavioural tagging is unknown. Here we show that retrieval of a LTM formed by behavioural tagging of a weak experience depends on the degree of overlap with the neuronal ensemble corresponding to a novel experience. The numbers of neurons activated by weak training in a novel object recognition (NOR) task and by a novel context exploration (NCE) task, denoted as overlapping neurons, increases in the hippocampal CA1 when behavioural tagging is successfully achieved. Optical silencing of an NCE-related ensemble suppresses NOR–LTM retrieval. Thus, a population of cells recruited by NOR is tagged and then preferentially incorporated into the memory trace for NCE to achieve behavioural tagging.
Suggested Citation
Masanori Nomoto & Noriaki Ohkawa & Hirofumi Nishizono & Jun Yokose & Akinobu Suzuki & Mina Matsuo & Shuhei Tsujimura & Yukari Takahashi & Masashi Nagase & Ayako M. Watabe & Fusao Kato & Kaoru Inokuchi, 2016.
"Cellular tagging as a neural network mechanism for behavioural tagging,"
Nature Communications, Nature, vol. 7(1), pages 1-11, November.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12319
DOI: 10.1038/ncomms12319
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Cited by:
- Akinobu Suzuki & Sakurako Kosugi & Emi Murayama & Eri Sasakawa & Noriaki Ohkawa & Ayumu Konno & Hirokazu Hirai & Kaoru Inokuchi, 2022.
"A cortical cell ensemble in the posterior parietal cortex controls past experience-dependent memory updating,"
Nature Communications, Nature, vol. 13(1), pages 1-14, December.
- Masanori Nomoto & Emi Murayama & Shuntaro Ohno & Reiko Okubo-Suzuki & Shin-ichi Muramatsu & Kaoru Inokuchi, 2022.
"Hippocampus as a sorter and reverberatory integrator of sensory inputs,"
Nature Communications, Nature, vol. 13(1), pages 1-15, December.
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