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Deep-Sea Coral Garden Invertebrates and Their Associated Fungi Are Genetic Resources for Chronic Disease Drug Discovery

机译:深海珊瑚园无脊椎动物及其相关的真菌是慢性病药物发现的遗传资源

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摘要

Chronic diseases characterized by bone and cartilage loss are associated with a reduced ability of progenitor cells to regenerate new tissues in an inflammatory environment. A promising strategy to treat such diseases is based on tissue repair mediated by human mesenchymal stem cells (hMSCs), but therapeutic outcomes are hindered by the absence of small molecules to efficiently modulate cell behaviour. Here, we applied a high-throughput drug screening technology to bioprospect a large library of extracts from Irish deep-sea organisms to induce hMSC differentiation toward musculoskeletal lineages and reduce inflammation of activated macrophages. The library included extracts from deep-sea corals, sponges and filamentous fungi representing a novel source of compounds for the targeted bioactivity. A validated hit rate of 3.4% was recorded from the invertebrate library, with cold water sea pens (octocoral order Pennatulacea), such as Kophobelemnon sp. and Anthoptilum sp., showing the most promising results in influencing stem cell differentiation toward osteogenic and chondrogenic lineages. Extracts obtained from deep-sea fungi showed no effects on stem cell differentiation, but a 6.8% hit rate in reducing the inflammation of activated macrophages. Our results demonstrate the potential of deep-sea organisms to synthetize pro-differentiation and immunomodulatory compounds that may represent potential drug development candidates to treat chronic musculoskeletal diseases.
机译:以骨和软骨损失为特征的慢性病与祖细胞在炎症环境中再生新组织的能力降低有关。治疗这种疾病的有希望的策略是基于由人间充质干细胞(HMSCs)介导的组织修复,但是通过不存在小分子来阻碍治疗结果以有效调节细胞行为。在这里,我们将高通量的药物筛查技术应用于生物保护大型萃取物,从爱尔兰深海生物中诱导HMSC分化对肌肉骨骼谱系,并减少活化巨噬细胞的炎症。该文库包括来自深海珊瑚,海绵和丝状真菌的提取物,代表靶向生物活性的新型化合物来源。验证的命中率为3.4%,从无脊椎动物库中记录,冷水海笔(八陶瓷秩序Pennatulacea),如kophobelemnon sp。和Anthophitum sp。,显示最有前途的导致影响干细胞分化对成骨和软骨形成谱系。从深海真菌中获得的提取物对干细胞分化没有影响,但在减少活化巨噬细胞的炎症时的击中率为6.8%。我们的结果表明,深海生物体对综合分化和免疫调节性化合物的潜力,这些化合物可能代表潜在的药物开发候选者来治疗慢性肌肉骨骼疾病。

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