| Literature DB >> 21345313 |
Sinsuk Han1, Jihye Koo, Jingyu Bae, Soochan Kim, Song Baik, Mi-Yeon Kim.
Abstract
Toll-like receptors (TLRs), which recognize structurally conserved components among pathogens, are mainly expressed by antigen-presenting cells such as dendritic cells (DCs), B cells, and macrophages. Recognition through TLRs triggers innate immune responses and influences antigen-specific adaptive immune responses. Although studies on the expression and functions of TLRs in antigen-presenting cells have been extensively reported, studies in lymphoid tissue inducer (LTi) cells have been limited. In this study, we observed that LTi cells expressed TLR2 and TLR4 mRNA as well as TLR2 protein and upregulated OX40L, CD30L, and TRANCE expression after stimulation with the TLR2 ligand zymosan or TLR4 ligand LPS. The expression of tumor necrosis factor superfamily (TNFSF) members was significantly upregulated when cells were cocultured with DCs, suggesting that upregulated TNFSF expression may contribute to antigen-specific adaptive immune responses.Entities:
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Year: 2011 PMID: 21345313 DOI: 10.5483/BMBRep.2011.44.2.129
Source DB: PubMed Journal: BMB Rep ISSN: 1976-6696 Impact factor: 4.778