Sleep deficiency exacerbates periodontal inflammation via trigeminal TRPV1 neurons

J Junhui Li (Department of Molecular, Cell, and Cancer Biology, University of Massachusetts Chan Medical School) Z Zhicheng Cui H Hongyu Gong Y Yan Zhang Z Zhenlin Yuan (Shanghai Engineering Research Center of Tooth Restoration and Regeneration and Tongji Research Institute of Stomatology and Department of Implantology, Shanghai Tongji Stomatological Hospital and Dental School, Tongji University) Z Zihao Zhang (Shanghai Engineering Research Center of Tooth Restoration and Regeneration and Tongji Research Institute of Stomatology and Department of Implantology, Shanghai Tongji Stomatological Hospital and Dental School, Tongji University) Z Zengyi Ma (Department of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University) N Nan Zhou (Key Laboratory of Functional Polymer Materials of Ministry of Education; Tianjin Key Laboratory of Functional Polymer Materials; Institute of Polymer Chemistry, College of Chemistry) C Chuanxin Huang (Department of Dermatology, Center for Immune-Related Diseases at Shanghai Institute of Immunology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine) Y Yao Zhao X Xia Li Z Zhi Zhang Y Yao Sun (Wuya College of Innovation)

Abstract

Periodontitis, a prevalent chronic inflammatory disease, profoundly impacts both quality of life and overall health. Clinical studies have suggested a correlation between periodontitis and sleep deficiency, but the underlying mechanisms involved remain elusive. Here, we observed an elevated risk of periodontitis in individuals with sleep deficiency, as demonstrated in both clinical subjects and mouse models. Retrograde tracing from the periodontium revealed a neural connection from trigeminal TRPV1 neurons, which may mediate the aggravating effects of sleep deficiency on periodontitis. The ablation of TRPV1 neurons effectively mitigated the aggravating effects of sleep deficiency on periodontitis. Under periodontitis, sleep restriction increased the secretion of substance P from trigeminal neurons in the periodontium, enhancing vasodilation and vascular permeability, which in turn promoted the infiltration of proinflammatory immune cells. Blocking substance P signaling via a Neurokinin-1 receptor antagonist or knocking down Tacr1 in vascular endothelial cells alleviated these detrimental effects. Our findings unveil a critical neuron-vessel-immune axis that exacerbates periodontitis during sleep deficiency and suggest potential therapeutic strategies targeting this axis for managing periodontitis in individuals suffering from sleep deficiency.

Article Details

Volume / Issue Vol. 122, Issue 24
Published June 17, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (13)

J

Junhui Li

Department of Molecular, Cell, and Cancer Biology, University of Massachusetts Chan Medical School

Z

Zhicheng Cui

H

Hongyu Gong

Y

Yan Zhang

Z

Zhenlin Yuan

Shanghai Engineering Research Center of Tooth Restoration and Regeneration and Tongji Research Institute of Stomatology and Department of Implantology, Shanghai Tongji Stomatological Hospital and Dental School, Tongji University

Z

Zihao Zhang

Shanghai Engineering Research Center of Tooth Restoration and Regeneration and Tongji Research Institute of Stomatology and Department of Implantology, Shanghai Tongji Stomatological Hospital and Dental School, Tongji University

Z

Zengyi Ma

Department of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University

N

Nan Zhou

Key Laboratory of Functional Polymer Materials of Ministry of Education; Tianjin Key Laboratory of Functional Polymer Materials; Institute of Polymer Chemistry, College of Chemistry

C

Chuanxin Huang

Department of Dermatology, Center for Immune-Related Diseases at Shanghai Institute of Immunology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

Y

Yao Zhao

X

Xia Li

Z

Zhi Zhang

Y

Yao Sun

Wuya College of Innovation