Cell‐Type Specific Circuits in the Mammillary Body for Place and Object Recognition Memory

Author:

Li Lanfang123,Guo Yiqing123,Jing Wei124,Tang Xiaomei123,Zeng Jinyu123,Hou Zhenye123,Song Yige123,He Aodi124,Li Hao123,Zhu Ling‐Qiang123,Lu Youming125ORCID,Li Xinyan124ORCID

Affiliation:

1. Wuhan Center of Brain Science Huazhong University of Science and Technology Wuhan 430030 China

2. Innovation Center of Brain Medical Sciences Ministry of Education of the People's Republic of China Wuhan 430030 China

3. Department of Pathophysiology School of Basic Medicine and Tongji Medical College Huazhong University of Science and Technology Wuhan 430030 China

4. Department of Anatomy School of Basic Medicine and Tongji Medical College Huazhong University of Science and Technology Wuhan 430030 China

5. Department of Physiology School of Basic Medicine and Tongji Medical College Huazhong University of Science and Technology Wuhan 4030030 China

Abstract

AbstractMammillary body (MB) is traditionally viewed as a structural node of an anatomic circuit for emotion and memory. However, little is known about its molecular and cellular organizations. Here, a discovery that MB contains four subtypes of neurons that occupy different spatial subregions is reported. Of these, two subtypes of neurons are tagged by parvalbumin (PV) and dopamine receptor‐D2 (Drd2) markers. PV neurons are spontaneously active, whereas Drd2 neurons are inactive at rest and generate rebound bursts. These two distinct electrophysiological properties are encoded by Kcnn4 and Cacna1h. PV and Drd2 neurons generate two distinct cell‐type specific circuits by receiving inputs from two discrete subiculum neuronal classes. Gain‐ and loss‐of‐function studies on these cortical‐subcortical circuits demonstrate their differential roles for place and object recognition memory. This finding provides a comprehensive molecular and structural atlas of MB neurons at single‐cell resolution and reveals that MB contains molecularly, structurally, and functionally dissociable streams within its serial architecture.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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