EphB2-dependent prefrontal cortex activation promotes long-range social approach and partner responsiveness

Author:

He Li-Na12ORCID,Chen Si12,Yang Qi12ORCID,Wu Zheng1,Lao Zheng-Kai12,Tang Chang-Fei12,Song Jiao-Jiao1,Liu Xian-Dong3,Lu Jiangteng12,Xu Xiao-Hong4,Chen Jin-Jin1,Xu Tian-Le12ORCID,Sun Suya3,Xu Nan-Jie1256ORCID

Affiliation:

1. Research Center of Translational Medicine, Shanghai Children’s Hospital, Department of Anatomy and Physiology, Shanghai Jiao Tong University School of Medicine, Shanghai 200062, China

2. Songjiang Institute, Songjiang District Central Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 201699, China

3. Department of Neurology and Institute of Neurology, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China

4. Institute of Neuroscience and State Key Laboratory of Neuroscience, Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai 200031, China

5. Shanghai Key Laboratory of Reproductive Medicine, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China

6. Key Laboratory of Cell Differentiation and Apoptosis of Chinese Ministry of Education, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China

Abstract

Social behavior starts with dynamic approach prior to the final consummation. The flexible processes ensure mutual feedback across social brains to transmit signals. However, how the brain responds to the initial social stimuli precisely to elicit timed behaviors remains elusive. Here, by using real-time calcium recording, we identify the abnormalities of EphB2 mutant with autism-associated Q858X mutation in processing long-range approach and accurate activity of prefrontal cortex (dmPFC). The EphB2-dependent dmPFC activation precedes the behavioral onset and is actively associated with subsequent social action with the partner. Furthermore, we find that partner dmPFC activity is responsive coordinately to the approaching WT mouse rather than Q858X mutant mouse, and the social defects caused by the mutation are rescued by synchro-optogenetic activation in dmPFC of paired social partners. These results thus reveal that EphB2 sustains neuronal activation in the dmPFC that is essential for the proactive modulation of social approach to initial social interaction.

Funder

MOST | National Key Research and Development Program of China

National Natural Science Foundation of China

State Key Laboratory of Neuroscience

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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