Djordjevic Michael A, Bezos Anna, Marmuse Laurence, Driguez Hugues, Samain Eric, Vauzeilles Boris, Beau Jean-Marie, Kordbacheh Farzaneh, Rolfe Barry G, Schwörer Ralf, Daines Alison M, Gresshoff Peter M, Parish Christopher R
Research School of Biology, Plant Science Division, College of Medicine, Biology and the Environment, Australian National University, Canberra, ACT, Australia.
John Curtin School of Medical Research, College of Medicine, Biology and the Environment, Australian National University, Canberra, ACT, Australia.
PLoS One. 2014 Dec 23;9(12):e112635. doi: 10.1371/journal.pone.0112635. eCollection 2014.
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.
脂壳寡糖(LCOs)是生态和农业上重要的细菌和真菌与多种陆地植物建立共生关系所需的信号分子。在植物中,寡聚壳聚糖和LCOs可以与不同的溶素基序(LysM)受体发生不同的相互作用,并影响先天免疫反应或共生相关途径。在动物中,寡聚壳聚糖也能诱导先天免疫和其他生理反应,但尚未证实其对LCO的识别作用。在此研究中,LCO和类LCO化合物通过调节血管生成在哺乳动物中呈现出结构依赖性的生物活性,血管生成是一个涉及从现有血管诱导和生长新血管的严格调控过程。对24种LCO、类LCO或寡聚壳聚糖化合物的测试结果表明,它们在体外对血管生成具有结构依赖性影响,可导致促进、抑制或无影响。与植物一样,哺乳动物中LCO的生物活性取决于末端取代基的存在和类型。类似链长的未取代寡聚壳聚糖无法调节血管生成,这表明哺乳动物细胞与植物细胞一样,能够区分LCO和未取代的寡聚壳聚糖。确定了生物活性LCOs在哺乳动物中的细胞作用模式。内皮细胞对玻连蛋白或纤连蛋白的黏附受到的刺激或抑制与其促血管生成或抗血管生成活性相关。重要的是,新型且更易于合成的类LCO二糖分子也具有生物活性,并且已证明脱乙酰壳二糖是识别的主要结构基础。基于此,合成并纯化了基于生物活性LCO结构的更简单的几丁质二糖衍生物,这些衍生物在哺乳动物细胞中显示出生物活性。由于重要的慢性疾病状态与血管生成不足或过度有关,LCO和类LCO分子可能有潜力成为一类新型的基于碳水化合物的调节血管生成疗法。