Li Ruiqi, Gu Fan, Peng Linlin, Huan Tingting, Zhou Zhuo, Song Yaling, He Jinmei, Ye Kaili, Sun Yao, Li Tiejun, He Miao, Bian Zhuan, Yin Wei
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University, Wuhan, 430079, China.
Department of Cariology and Endodontics (I), Hospital of Stomatology, Wuhan University, Wuhan, 430079, China.
Adv Sci (Weinh). 2025 Jan;12(1):e2406684. doi: 10.1002/advs.202406684. Epub 2024 Oct 28.
Tertiary lymphoid structure (TLS) is associated with various pathologies, including those of cancers and chronic infections. Depending on the organ, multiple factors regulate the formation of TLS. However, the role of TLS in immune response and the molecules that drive its formation remain uncertain. The dental pulp, includes a few immune cells surrounded by rigid mineralized tissue, and opens to the outside through the apical foramen. Owing to this special organization, the dental pulp generates a directional immune response to bacterial infection. Considering this aspect, the dental pulp is an ideal model for comprehensively studying the TLS. In the present study, single-cell RNA sequencing of healthy and inflamed human dental pulp reveals known markers of TLS, including C-C motif chemokine ligand 19 (CCL19), lysosome-associated membrane glycoprotein 3 (LAMP3), CC chemokine receptor 7 (CCR7), and CD86, present in inflamed dental pulp. Compared with the healthy pulp, types and proportions of immune cells increase, along with enhanced cellular communication. Multiple immunofluorescence staining reveals that typical TLS emerges in dental pulp with pulpitis, consistent with the high expression of CC chemokine ligand 3 (CCL3), which may be a key driver of TLS formation. Moreover, TLS is also observed in a mouse model of pulpitis. These findings collectively offer insights into the formation and function of TLS in response to infection.
三级淋巴结构(TLS)与多种病理状况相关,包括癌症和慢性感染等。根据器官的不同,多种因素调节TLS的形成。然而,TLS在免疫反应中的作用以及驱动其形成的分子仍不明确。牙髓包含一些被坚硬矿化组织包围的免疫细胞,并通过根尖孔与外界相通。由于这种特殊的组织结构,牙髓对细菌感染产生定向免疫反应。考虑到这一方面,牙髓是全面研究TLS的理想模型。在本研究中,对健康和发炎的人牙髓进行单细胞RNA测序,揭示了TLS的已知标志物,包括C-C基序趋化因子配体19(CCL19)、溶酶体相关膜糖蛋白3(LAMP3)、CC趋化因子受体7(CCR7)和CD86,这些标志物存在于发炎的牙髓中。与健康牙髓相比,免疫细胞的类型和比例增加,细胞间通讯也增强。多重免疫荧光染色显示,典型的TLS在牙髓炎的牙髓中出现,这与CC趋化因子配体3(CCL3)的高表达一致,CCL3可能是TLS形成的关键驱动因素。此外,在牙髓炎小鼠模型中也观察到了TLS。这些发现共同为TLS在应对感染时的形成和功能提供了见解。