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Mapping of the proinflammatory domains of MspTL of Treponema lecithinolyticum

¹ Department of Oral Microbiology and Immunology, School of Dentistry, Seoul National University, Seoul 110-749, Republic of Korea
² Dental Research Institute, School of Dentistry, Seoul National University, Seoul 110–749, Republic of Korea

Correspondence
Bong-Kyu Choi
bongchoi{at}snu.ac.kr

The major surface protein (MspTL) of Treponema lecithinolyticum, associated with periodontitis and endodontic infections, has been reported to induce proinflammatory mediators such as intercellular adhesion molecule (ICAM)-1, and interleukin (IL)-1β, IL-6 and IL-8. The purpose of this study was to examine the role of MspTL in cell adhesion/migration and to identify its proinflammatory domains. Using the human monocytic cell line THP-1 and human dermal microvascular endothelial cells (HMEC-1), it was demonstrated that MspTL increased adhesion of monocytes to endothelial cells and transendothelial migration. To analyse the proinflammatory domains of the protein, four gene constructs covering different regions of MspTL were designed and expressed in Escherichia coli using the expression vector pQE-30. Histidine-tagged recombinant proteins were purified using Ni-NTA agarose and polymyxin B agarose to remove LPS contamination. Recombinant truncated polypeptides were assessed for the ability to induce ICAM-1 and proinflammatory factors in THP-1 cells by real-time RT-PCR and ELISA. Of the four polypeptides, the one spanning the N-terminal 86 amino acids significantly induced ICAM-1, IL-1β, IL-6, IL-8, tumour necrosis factor- (TNF-), cyclooxygenase (COX)-2, and prostaglandin E₂ (PGE₂). The results indicate that MspTL may induce cell adhesion and inflammation via its N-terminal region.