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Expression of functional Toll‐like receptors and nucleotide‐binding oligomerization domain proteins in murine cementoblasts and their upregulation during cell differentiation
Author(s) -
Nemoto E.,
Honda T.,
Kanaya S.,
Takada H.,
Shimauchi H.
Publication year - 2008
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.2008.01096.x
Subject(s) - cementoblast , microbiology and biotechnology , chemistry , biology , cementum , medicine , pathology , dentin
Background and Objective: While the primary role of cementoblasts is to synthesize the components of cementum, we have reported that immortalized murine cementoblasts (OCCM‐30) express functional Toll‐like receptor (TLR)‐2 and ‐4, and these receptors are involved in the alteration of gene expression associated with cementum formation and in the upregulation of osteoclastogenesis‐associated molecules, such as receptor activator of nuclear factor‐κB (NF‐κB) ligand. We hypothesized that cementoblasts express a wide range of pattern recognition receptors in a manner comparable to osteoblasts, which are known to express various functional TLRs and nucleotide‐binding oligomerization domain (NOD) proteins. Material and Methods: Murine cementoblasts and pre‐osteoblasts were used. The gene and protein levels of TLRs/NODs were analyzed using real‐time polymerase chain reaction and flow cytometry. Interleukin‐6 (IL‐6) and activated NF‐κB were measured using enzyme‐linked immunosorbent assay. Results: The expressions of TLR‐1, ‐2, ‐4, ‐6 and ‐9, CD14, NOD‐1 and ‐2 were detected in cementoblasts and were upregulated upon differentiation induced by ascorbic acid. Similar patterns were observed in the mouse MC3T3‐E1 osteoblast cell line. Synthetic ligands, Pam3CSK4 (TLR‐1/2 agonist), Pam2CGDPKHPKSF (TLR‐2/6 agonist), lipid A (TLR4 agonist), CpG DNA (TLR‐9 agonist), FK565 (NOD1 agonist) and muramyldipeptide (NOD2 agonist), effectively induced NF‐κB activation in cementoblasts and/or ascorbic acid‐treated cementoblasts. Furthermore, these ligands induced IL‐6 production in a NF‐κB‐dependent manner in cementoblasts and/or ascorbic acid‐treated cementoblasts. Conclusion: These results indicate that cementoblasts possess functional TLR and NOD signaling systems and have a similar capacity to osteoblasts in responding to a wide variety of pathogens.