Open AccessThe diacylated lipopeptide FSL‐1 enhances phagocytosis of bacteria by macrophages through a Toll‐like receptor 2‐mediated signalling pathway
Author(s) -
Mae Masako,
Iyori Mitsuhiro,
Yasuda Motoaki,
Shamsul Haque Mohammad,
Kataoka Hideo,
Kiura Kazuto,
Hasebe Akira,
Totsuka Yasunori,
Shibata Kenichiro
Publication year - 2007
Publication title -
fems immunology & medical microbiology
Language(s) - English
Resource type - Journals
eISSN - 1574-695X
pISSN - 0928-8244
DOI - 10.1111/j.1574-695x.2007.00218.x
Subject(s) - phagocytosis , tlr2 , biology , microbiology and biotechnology , receptor , toll like receptor , scavenger receptor , downregulation and upregulation , cd14 , innate immune system , biochemistry , lipoprotein , cholesterol , gene
A significant amount of evidence has been accumulated to show that Toll‐like receptors (TLRs) function as sensors for microbial invasion. However, little is known about how signalling triggered by TLRs leads to the phagocytosis of pathogens. This study was designed to determine whether stimulation of TLR2 mainly with the lipopeptide FSL‐1 plays a role in the phagocytosis of pathogens by macrophages. FSL‐1 enhanced the phagocytosis of Escherichia coli to a markedly greater extent than it did that of Staphylococcus aureus , but did not enhance the phagocytosis of latex beads. FSL‐1 stimulation resulted in enhanced phagocytosis of bacteria by macrophages from TLR2 +/+ mice but not by those from TLR2 −/− mice. Chinese hamster ovary cells stably expressing TLR2 failed to phagocytose these bacteria, but the cells expressing CD14 did. FSL‐1 induced upregulation of the expression of phagocytic receptors, including MSR1, CD36, DC‐SIGN and Dectin‐1 in THP‐1 cells. Human embryonic kidney 293 cells transfected with DC‐SIGN and MSR1 phagocytosed these bacteria. These results suggest that the FSL‐1‐induced enhancement of phagocytosis of bacteria by macrophages may be explained partly by the upregulation of scavenger receptors and the C‐type lectins through TLR2‐mediated signalling pathways, and that TLR2 by itself does not function as a phagocytic receptor.