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Tertiary Lymphoid Structure in Dental Pulp: The Role in Combating Bacterial Infections. | LitMetric

Tertiary Lymphoid Structure in Dental Pulp: The Role in Combating Bacterial Infections.

Adv Sci (Weinh)

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.

Published: October 2024

AI Article Synopsis

  • - Tertiary lymphoid structures (TLS) are linked to various diseases, such as cancers and chronic infections, but their role in immune responses and formation processes is not completely understood.
  • - The dental pulp, with its unique immune cell organization and connection to the outside environment, provides a valuable model for studying TLS and immune responses to bacterial infections.
  • - Single-cell RNA sequencing and immunofluorescence staining in healthy versus inflamed dental pulp reveal markers and increased immune cell activity, indicating that TLS forms in inflamed conditions and may be driven by molecules like CCL3.

Article Abstract

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.

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Source
http://dx.doi.org/10.1002/advs.202406684DOI Listing

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