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绿海龟 cathelicidins 的多样性、免疫调节作用和构效关系。

Diversity, immunoregulatory action and structure-activity relationship of green sea turtle cathelicidins.

机构信息

School of Bioengineering, Dalian University of Technology, Dalian, Liaoning, 116024, China.

Department of Pharmaceutical Sciences, College of Pharmaceutical Sciences, Soochow University, Suzhou, Jiangsu, 215123, China.

出版信息

Dev Comp Immunol. 2019 Sep;98:189-204. doi: 10.1016/j.dci.2019.05.005. Epub 2019 May 20.

Abstract

Cathelicidins are a family of gene-encoded immune effectors in vertebrate innate immunity. Here, we reported the diversity and biological activity of cathelicidins in green sea turtle, a marine reptile species known for long lifespan and disease resistance. Four novel cathelicidins (Cm-CATH1-4) were identified from green sea turtle. All of them, especially Cm-CATH2, exhibited potent, broad-spectrum and rapid bactericidal and anti-biofilm activities by inducing the disruption of cell membrane integrity. Additionally, Cm-CATH2 effectively induced the macrophages/monocytes and neutrophils trafficking to the infection site, and inhibited the LPS-induced production of inflammatory cytokines, by blocking TLR4/MD2 complex and the downstream signaling pathway activation. In mouse peritonitis and pneumonia models, Cm-CATH2 exhibited evident protection against drug-resistant bacterial infections. Taken together, the diverse structures and functions of Cm-CATHs indicated their pleiotropic role in innate immunity of green sea turtle, and the potent antimicrobial, anti-biofilm and immunomodulatory properties make them ideal candidates for the development of novel anti-infective drugs.

摘要

鱼精蛋白是脊椎动物先天免疫中基因编码的免疫效应因子家族。在这里,我们报道了绿海龟(一种以长寿和抗疾病能力而闻名的海洋爬行动物)中鱼精蛋白的多样性和生物学活性。从绿海龟中鉴定出了四种新型鱼精蛋白(Cm-CATH1-4)。它们都具有强大、广谱和快速的杀菌和抗生物膜活性,通过诱导细胞膜完整性的破坏来实现。此外,Cm-CATH2 通过阻断 TLR4/MD2 复合物和下游信号通路的激活,有效诱导巨噬细胞/单核细胞和中性粒细胞向感染部位迁移,并抑制 LPS 诱导的炎症细胞因子的产生。在小鼠腹膜炎和肺炎模型中,Cm-CATH2 对耐药菌感染表现出明显的保护作用。综上所述,Cm-CATHs 的结构和功能多样性表明它们在绿海龟先天免疫中具有多功能作用,其强大的抗菌、抗生物膜和免疫调节特性使它们成为新型抗感染药物的理想候选药物。

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