• Michael D Liang, Aranya Bagchi, H Shaw Warren, Megan M Tehan, James A Trigilio, Laura K Beasley-Topliffe, Brenda L Tesini, Jean-Claude Lazzaroni, Matthew J Fenton, and Judith Hellman.
• Department of Pathology, Boston University Medical Center, Boston, Massachusetts, USA.
• J. Infect. Dis. 2005 Mar 15;191(6):939-48.

AbstractSepsis is initiated by interactions between microbial products and host inflammatory cells. Toll-like receptors (TLRs) are central innate immune mediators of sepsis that recognize different components of microorganisms. Peptidoglycan-associated lipoprotein (PAL) is a ubiquitous gram-negative bacterial outer-membrane protein that is shed by bacteria into the circulation of septic animals. We explored the inflammatory effects of purified PAL and of a naturally occurring form of PAL that is shed into serum. PAL is released into human serum by Escherichia coli bacteria in a form that induces cytokine production by macrophages and is tightly associated with lipopolysaccharide (LPS). PAL activates inflammation through TLR2. PAL and LPS synergistically activate macrophages. These data suggest that PAL may play an important role in the pathogenesis of sepsis and imply that physiologically relevant PAL and LPS are shed into serum and act in concert to initiate inflammation in sepsis.

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