
Yi-Quan Tang
Professor
Principal Investigator
Dr. Yi-Quan Tang received his Ph.D. in Neurobiology from Peking University in 2013. From 2014 to 2018, he conducted postdoctoral research at the MRC Laboratory of Molecular Biology in Cambridge, UK, where he was promoted to Investigator Scientist in early 2018. Since January 2021, he has served as a principal investigator at the Institutes of Brain Science, Fudan University, and the State Key Laboratory of Brain Function and Disorders.
Address: Institutes of Brain Science, Fudan University, 131 Dongan Road, Shanghai, China, 200032
Email:yqtang@@fudan.edu.cn
Brain-body interfaces
Continuous bidirectional communication and coordinated regulation between the brain and the body are essential for physiological homeostasis. The molecular sensors, neural pathways, and regulatory systems that support this communication constitute the body’s natural “brain-body interfaces.” These interfaces encompass the detection and input of bodily signals, their decoding and integration by the nervous system, and regulatory outputs through neural and neuroendocrine pathways. Dysfunction of these interfaces can impair normal physiological regulation and contribute to disease onset and progression. Understanding how they work offers new opportunities to regulate organ function through the nervous system.
Our laboratory pursues two interconnected research directions. The first is the discovery and mechanistic characterization of natural brain-body interfaces, addressing how the body and the brain communicate. With a focus on visceral sensation and mechanotransduction, we identify key molecular sensors and neuronal subpopulations, investigate how bodily signals are detected, transmitted, and integrated to guide physiological regulation, and determine how these mechanisms contribute to respiratory control, cardiovascular function, feeding behavior, and related diseases. The second is the development of artificial brain-body interfaces and targeted therapeutics, addressing how to access brain-body communication pathways to regulate organ function. Guided by the working principles of natural brain-body interfaces, we aim to integrate joint monitoring of brain activity and bodily physiological states, brain-body signal decoding, and neuromodulatory outputs to develop closed-loop artificial brain-body interfaces for coordinated regulation of the brain and body. In parallel, we screen and functionally validate drug candidates that target key molecular sensors and their regulatory mechanisms. Through these technological and pharmacological approaches, we seek to translate basic discoveries into therapeutic interventions.
Our work has been published in Neuron, Circulation Research, Advanced Science, and Cell Reports, with Dr. Tang serving as corresponding or co-corresponding author. Our research has been supported by multiple national and international programs, including the General Program of the National Natural Science Foundation of China (NSFC; two grants, 2022–2025 and 2027–2030, principal investigator); the NSFC Innovative Research Group Program, Type A (2026–2030, core team member); the National Key R&D Program of China (2024–2027, subproject leader); the STI2030 Major Project on Brain Science and Brain-Inspired Intelligence (2021–2026, core team member); and the Novo Nordisk ValidatioNN Award (2025–2026, principal investigator).
Wang HK#, Yang ZK#, Zhong BR#, Gong TY, Liu DD, Pan ZW, Shen JX, Wang YG, Fan XZ, Zhang XT, Gao F, Fan HP, Guo WP, Qiu HY, Dong XX, Cao YH, Chen JH, Ma H, Tang YQ*, Liang P* (2026). TMC6 Is a Novel Therapeutic Target for Pathogenic Cardiac Hypertrophy. Circ Res. 138(7): e327680.
Wang Z#, Tang QH#, Li K#, Mou JH, Chen YY, Kuang WQ, Sun LT, Ma ZY, Wei YR, Bao R, Sun XH, Wang SL, Lu W, Xu GY, Tang YQ*, Duan SM*, Ni JD* (2026). An enteric-DRG pathway for interoception and visceral pain in mice. Neuron. 114(1): 105-121.e6.
Zhang YZ, You D, Che CH, Wang XY, Li HW*, Tang YQ*, Sun S* (2025). Ototoxicity-induced c-Fos activation underlies the regenerative capacity of the vestibular sensory epithelia. Cell Commun Signal. 23(1): 421.
Chen P#, Che CH#, Wu LJ#, Sun CJ, Xu DM, Hua QY, Zhang YZ, Tang YQ*, Shi P*, Sun S* (2025). Comparative Cochlear Transcriptomics in Echolocating Bats and Mouse Reveals Hras as Protector Against Noise-Induced Hearing Loss. Adv Sci. 12(44): e08466.
Tang YQ*, Lee SA, Rahman M, Vanapalli SA, Lu H, Schafer WR* (2020). Ankyrin Is an Intracellular Tether for TMC Mechanotransduction Channels. Neuron. 107(1): 112-125.e10.