SR-A, MARCO and TLRs differentially recognise selected surface proteins from Neisseria meningitidis: an example of fine specificity in microbial ligand recognition by innate immune receptors

Journal article

Macrophages express various classes of pattern recognition receptors involved in innate immune recognition of artificial, microbial and host-derived ligands. These include the scavenger receptors (SRs), which are important for phagocytosis, and the Toll-like receptors (TLRs) involved in microbe sensing. The class A macrophage scavenger receptor (SR-A) and macrophage receptor with a collagenous structure (MARCO) display similar domain structures and ligand-binding specificity, which has led to the assumption that these two receptors may be functionally redundant. In this study we show that SR-A and MARCO differentially recognise artificial polyanionic ligands as well as surface proteins from the pathogenic bacterium Neisseria meningitidis. We show that, while acetylated low-density lipoprotein (AcLDL) is a strong ligand for SR-A, it is not a ligand for MARCO. Of the neisserial proteins that were SR ligands, some were ligands for both receptors, while other proteins were only recognised by either SR-A or MARCO. We also analysed the potential of these ligands to act as TLR agonists and assessed the requirement for SR-A and MARCO in pro-inflammatory cytokine induction. SR ligation alone did not induce cytokine production; however, for proteins that were both SR and TLR ligands, the SRs were required for full activation of TLR pathways.

Authors: Plüddemann, A; Mukhopadhyay, S; Sankala, M; Savino, S; Pizza, M

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Karger Publishers
• Journal: Journal of Innate Immunity
• Volume: 1
• Issue: 2
• Pages: 153-163
• Publication date: 2008-09-11
• Acceptance date: 2008-06-23
• DOI: 10.1159/000155227
• EISSN: 1662-8128
• ISSN: 1662-811X
• Language: English
• Keywords: cytokine; macrophage; scavenger receptor; toll-like receptor; neisseria; ligand; receptor collaboration