Encoding of social novelty by sparse GABAergic neural ensembles in the prelimbic cortex

Author:

Zhao Zhe1ORCID,Zeng Fengqingyang2ORCID,Wang Hanbin3ORCID,Wu Runlong4ORCID,Chen Liping1,Wu Yan1,Li Shen1,Shao Jingyuan1ORCID,Wang Yao3,Wu Junjie2,Feng Zhiheng3ORCID,Gao Weizheng3,Hu Yanhui5,Wang Aimin6,Cheng Heping4ORCID,Zhang Jue23ORCID,Chen Liangyi478ORCID,Wu Haitao1910ORCID

Affiliation:

1. Department of Neurobiology, Beijing Institute of Basic Medical Sciences, 100850 Beijing, China.

2. College of Engineering, Peking University, 100871 Beijing, China.

3. Academy of Advanced Interdisciplinary Study, Peking University, 100871 Beijing, China.

4. State Key Laboratory of Membrane Biology, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking-Tsinghua Center for Life Sciences, College of Future Technology, Peking University, 100871 Beijing, China.

5. Beijing Transcend Vivoscope Biotech Co. Ltd., 100094 Beijing, China.

6. State Key Laboratory of Advanced Optical Communication System and Networks, School of Electronics, Peking University, 100871 Beijing, China.

7. PKU-IDG/McGovern Institute for Brain Research, 100871 Beijing, China.

8. National Biomedical Imaging Center, Beijing 100871, China.

9. Key Laboratory of Neuroregeneration, Coinnovation Center of Neuroregeneration, Nantong University, Nantong 226019, Jiangsu Province, China.

10. Chinese Institute for Brain Research, 102206 Beijing, China.

Abstract

Although the prelimbic (PrL) area is associated with social behaviors, the neural ensembles that regulate social preference toward novelty or familiarity remain unknown. Using miniature two-photon microscopy (mTPM) to visualize social behavior–associated neuronal activity within the PrL in freely behaving mice, we found that the Ca 2+ transients of GABAergic neurons were more highly correlated with social behaviors than those of glutamatergic neurons. Chemogenetic suppression of social behavior–activated GABAergic neurons in the PrL disrupts social novelty behaviors. Restoring the MeCP2 level in PrL GABAergic neurons in MECP2 transgenic ( MECP2 -TG) mice rescues the social novelty deficits. Moreover, we identified and characterized sparsely distributed NewPNs and OldPNs of GABAergic interneurons in the PrL preferentially responsible for new and old mouse exploration, respectively. Together, we propose that social novelty information may be encoded by the responses of NewPNs and OldPNs in the PrL area, possibly via synergistic actions on both sides of the seesaw.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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