Trophoblast giant (TG) cells, components cells of the mouse placenta, exhibit phagocytic activity, and participate in the placental defense system by extracellular bacterial antigen uptake via phagocytosis. However, the bacterial uptake mechanisms by TG cells remain to be entirely understood. In an attempt to understand these mechanisms, in this study, we investigated the pattern recognition receptors (PRRs) involved in phagocytosis by TG cells. PRRs such as Toll-like receptors (TLRs) and scavenger receptors play a critical role in the immune response to bacterial pathogens. Among these, we selected TLR2 and class B scavenger receptor type I (SR-BI) and then evaluated their properties in TG cells. TLR2 and SR-BI expression is higher in TG cells than in trophoblast stem (TS) cells. Although interferon-γ treatment activated bacterial uptake in a concentration-dependent manner, it did not induce TLR2 or SR-BI expression. Depletion of TLR2 and SR-BI by siRNA reduced the bacterial uptake ability of TG cells, which was also affected by treatment with the TLR2 agonist triacylated lipopeptide. These results suggested that the phagocytic activity of TG cells is mediated by both TLR2 and SR-BI.
- Class B scavenger receptor type I
- Toll-like receptor 2
- Trophoblast giant cell
ASJC Scopus subject areas
- Molecular Biology