Abstract

Lipochitin oligosaccharides (LCOs) are signaling molecules required by ecologically and agronomically important bacteria and fungi to establish symbioses with diverse land plants. In plants, oligo-chitins and LCOs can differentially interact with different lysin motif (LysM) receptors and affect innate immunity responses or symbiosis-related pathways. In animals, oligo-chitins also induce innate immunity and other physiological responses but LCO recognition has not been demonstrated. Here LCO and LCO-like compounds are shown to be biologically active in mammals in a structure dependent way through the modulation of angiogenesis, a tightly-regulated process involving the induction and growth of new blood vessels from existing vessels. The testing of 24 LCO, LCO-like or oligo-chitin compounds resulted in structure-dependent effects on angiogenesis in vitro leading to promotion, or inhibition or nil effects. Like plants, the mammalian LCO biological activity depended upon the presence and type of terminal substitutions. Un-substituted oligo-chitins of similar chain lengths were unable to modulate angiogenesis indicating that mammalian cells, like plant cells, can distinguish between LCOs and un-substituted oligo-chitins. The cellular mode-of-action of the biologically active LCOs in mammals was determined. The stimulation or inhibition of endothelial cell adhesion to vitronectin or fibronectin correlated with their pro- or anti-angiogenic activity. Importantly, novel and more easily synthesised LCO-like disaccharide molecules were also biologically active and de-acetylated chitobiose was shown to be the primary structural basis of recognition. Given this, simpler chitin disaccharides derivatives based on the structure of biologically active LCOs were synthesised and purified and these showed biological activity in mammalian cells. Since important chronic disease states are linked to either insufficient or excessive angiogenesis, LCO and LCO-like molecules may have the potential to be a new, carbohydrate-based class of therapeutics for modulating angiogenesis.

Highlights

  • Lipochitin oligosaccharides (LCOs) are natural products synthesised by prokaryotic nitrogen fixing bacteria and eukaryotic arbuscular mycorrhizal (AM) fungi

  • These results show that, like plants, mammalian endothelial cells (ECs) can distinguish between LCOs and chitin oligosaccharides, even though these molecules share an oligo-chitin-like backbone

  • The results suggest that LCO structural specificity is required for strong anti-angiogenic activity on ECs and the most biologically active LCO molecules strongly resembled structures which affect soybean plants

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Summary

Introduction

Lipochitin oligosaccharides (LCOs) are natural products synthesised by prokaryotic nitrogen fixing bacteria (generically called ‘‘rhizobia’’) and eukaryotic arbuscular mycorrhizal (AM) fungi These naturally occurring molecules act as microbial signals that are required to establish nitrogen-fixing nodule formation and mycorrhization respectively. The lengths of the chitin backbone and terminal substitutions greatly influence the extent and specificity of LCO recognition by lysin motif (LysM) type receptors [1, 6, 7, 8]. In contrast to rhizobial and AM LCOs, different plant LysM-type receptors (e.g., LYK3 and LYK4) preferentially recognise chitin oligomers as microbe-associated molecular patterns (MAMPs) and this induces an innate, ‘general-immune’ response [10, 11, 12]. LCOs and chitin oligomers may share an affinity for chitin-motif recognising receptors the down-stream responses induced are different

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