Heterosynaptic plasticity of the visuo-auditory projection requires cholecystokinin released from entorhinal cortex afferents

Wenjian Sun (Co-first Author), Haohao Wu (Co-first Author), Yujie Peng (Co-first Author), Xuejiao Zheng (Co-first Author), Jing Li (Co-first Author), Dingxuan Zeng (Co-first Author), Peng Tang, Ming Zhao, Hemin Feng, Hao Li, Ye Liang, Junfeng Su, Xi Chen*, Tomas Hökfelt*, Jufang He*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Abstract

The entorhinal cortex is involved in establishing enduring visuo-auditory associative memory in the neocortex. Here we explored the mechanisms underlying this synaptic plasticity related to projections from the visual and entorhinal cortices to the auditory cortex in mice using optogenetics of dual pathways. High-frequency laser stimulation (HFS laser) of the visuo-auditory projection did not induce long-term potentiation. However, after pairing with sound stimulus, the visuo-auditory inputs were potentiated following either infusion of cholecystokinin (CCK) or HFS laser of the entorhino-auditory CCK-expressing projection. Combining retrograde tracing and RNAscope in situ hybridization, we show that Cck expression is higher in entorhinal cortex neurons projecting to the auditory cortex than in those originating from the visual cortex. In the presence of CCK, potentiation in the neocortex occurred when the presynaptic input arrived 200 ms before postsynaptic firing, even after just five trials of pairing. Behaviorally, inactivation of the CCK+ projection from the entorhinal cortex to the auditory cortex blocked the formation of visuo-auditory associative memory. Our results indicate that neocortical visuo-auditory association is formed through heterosynaptic plasticity, which depends on release of CCK in the neocortex mostly from entorhinal afferents. © Sun, Wu, Peng et al.
Original languageEnglish
Article numbere83356
JournaleLife
Volume13
Online published4 Mar 2024
DOIs
Publication statusPublished - 2024

Funding

This work was supported by Hong Kong Research Grants Council, General Research Fund: 11103220M, 11101521M (GRF, JFH); Hong Kong Research Grants Council, Collaborative Research Fund: C1043- 21GF(CRF, JFH); Innovation and Technology Fund: MRP/053/18X, GHP_075_19GD (ITF, JFH); Health and Medical Research Fund: 06172456, 09203656 (HMRF, XC, JFH); The Swedish Research Council: 2018-0273 (TH); The Arvid Carlsson Foundation (TH); The Swedish Research Council: 220-01688 (TH); Key-Area Research and Development Program of Guangdong Province: 2018B030340001 (WJS); and the following charitable foundations for their generous support to JFH: Wong Chun Hong Endowed Chair Professorship, Charlie Lee Charitable Foundation, and Fong Shu Fook Tong Foundation.

Research Keywords

  • Mice
  • Animals
  • Entorhinal Cortex/physiology
  • Cholecystokinin/metabolism
  • Long-Term Potentiation/physiology
  • Neuronal Plasticity/physiology
  • Neurons/metabolism

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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