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寄生线虫马来布鲁线虫分泌的微小RNA破坏淋巴管内皮细胞的完整性。

MicroRNAs secreted by the parasitic nematode Brugia malayi disrupt lymphatic endothelial cell integrity.

作者信息

Johnson Hailey, Banakis Stephanie, Chung Matthew, Ghedin Elodie, Voronin Denis

机构信息

Systems Genomics Section, Laboratory of Parasitic Diseases, Division of Intramural Research, NIAID, NIH, Bethesda, Maryland, United States of America.

出版信息

PLoS Negl Trop Dis. 2024 Dec 31;18(12):e0012803. doi: 10.1371/journal.pntd.0012803. eCollection 2024 Dec.

Abstract

Lymphatic filariasis (LF) is a neglected tropical disease affecting over 51 million people in 72 endemic countries. Causative agents of LF are mosquito-borne parasitic nematodes Wuchereria bancrofti, Brugia malayi, and Brugia timori. The adult parasites impact the integrity of lymphatic vessels and damage valves, leading to a remodeling of the lymphatic system and lymphatic dilation. Chronic infections can develop into severe clinical manifestations, primarily lymphedema, hydrocoele, and elephantiasis. Mechanistic studies on the underlying pathology due to the parasite are necessary to better manage human filariasis. Since parasite molecules, such as microRNAs (miRNAs), can be found in secreted extracellular vesicles (EVs) and are transported between parasite and host cells, we hypothesized that these could also play a role in the development of pathology in LF. In this study, we tested two B. malayi miRNAs previously detected in vitro in the culture media of microfilarial stages of worms. While one is Brugia-specific (bma-miR-5864) and the other nematode-specific (bma-miR-86), both miRNAs are secreted in high abundance. We first examined the in vitro response by transcriptomic profiling of human lymphatic endothelial cells to treatment with these miRNAs, which allowed us to identify genes involved in maintaining the integrity of the lymphatic endothelium. We then measured the effect of these miRNAs on the regulation of proteins necessary for cell integrity, demonstrating downregulation leading to a significant increase in the permeability of the endothelium monolayer. With this study we identify parasite miRNAs involved in undermining the integrity of endothelial cells, thus potentially contributing to the development of pathology. These findings could pave the way for a novel treatment strategy where the inhibition of parasite-secreted molecules could slow the progression of LF pathology. From a broader perspective, the miRNAs secreted by filarial parasites could potentially be used in the future for diagnosing and monitoring disease progression or treatment efficacy.

摘要

淋巴丝虫病(LF)是一种被忽视的热带疾病,在72个流行国家影响着超过5100万人。淋巴丝虫病的病原体是由蚊子传播的寄生线虫班氏吴策线虫、马来布鲁线虫和帝汶布鲁线虫。成年寄生虫会影响淋巴管的完整性并损害瓣膜,导致淋巴系统重塑和淋巴管扩张。慢性感染可发展为严重的临床表现,主要是淋巴水肿、鞘膜积液和象皮肿。对寄生虫引起的潜在病理机制进行研究,对于更好地控制人类丝虫病至关重要。由于寄生虫分子,如微小RNA(miRNA),可以在分泌的细胞外囊泡(EV)中被发现,并在寄生虫和宿主细胞之间运输,我们推测这些分子也可能在淋巴丝虫病的病理发展中发挥作用。在这项研究中,我们测试了之前在体外从丝虫微丝蚴阶段的培养基中检测到的两种马来布鲁线虫miRNA。其中一种是布鲁线虫特异性的(bma-miR-5864),另一种是线虫特异性的(bma-miR-86),这两种miRNA都大量分泌。我们首先通过对人淋巴管内皮细胞进行转录组分析,检测其对这些miRNA处理的体外反应,从而确定参与维持淋巴管内皮完整性的基因。然后,我们测量了这些miRNA对细胞完整性所需蛋白质调控的影响,结果表明其下调导致内皮单层通透性显著增加。通过这项研究,我们确定了参与破坏内皮细胞完整性的寄生虫miRNA,从而可能导致病理发展。这些发现可能为一种新的治疗策略铺平道路,即抑制寄生虫分泌的分子可能减缓淋巴丝虫病病理的进展。从更广泛的角度来看,丝虫寄生虫分泌的miRNA未来可能用于诊断和监测疾病进展或治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11706539/130dd9fff7b5/pntd.0012803.g001.jpg

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