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尖吻鲈(Lates calcarifer)DC-SCRIPT的鉴定,一种鱼类树突状细胞的特异性分子标记。

Identification of Barramundi (Lates calcarifer) DC-SCRIPT, a Specific Molecular Marker for Dendritic Cells in Fish.

作者信息

Zoccola Emmanuelle, Delamare-Deboutteville Jérôme, Barnes Andrew C

机构信息

The University of Queensland, School of Biological Sciences and Centre for Marine Science, Brisbane, Queensland, 4072, Australia.

出版信息

PLoS One. 2015 Jul 14;10(7):e0132687. doi: 10.1371/journal.pone.0132687. eCollection 2015.

Abstract

Antigen presentation is a critical step bridging innate immune recognition and specific immune memory. In mammals, the process is orchestrated by dendritic cells (DCs) in the lymphatic system, which initiate clonal proliferation of antigen-specific lymphocytes. However, fish lack a classical lymphatic system and there are currently no cellular markers for DCs in fish, thus antigen-presentation in fish is poorly understood. Recently, antigen-presenting cells similar in structure and function to mammalian DCs were identified in various fish, including rainbow trout (Oncorhynchus mykiss) and zebrafish (Danio rerio). The present study aimed to identify a potential molecular marker for DCs in fish and therefore targeted DC-SCRIPT, a well-conserved zinc finger protein that is preferentially expressed in all sub-types of human DCs. Putative dendritic cells were obtained in culture by maturation of spleen and pronephros-derived monocytes. DC-SCRIPT was identified in barramundi by homology using RACE PCR and genome walking. Specific expression of DC-SCRIPT was detected in barramundi cells by Stellaris mRNA FISH, in combination with MHCII expression when exposed to bacterial derived peptidoglycan, suggesting the presence of DCs in L. calcarifer. Moreover, morphological identification was achieved by light microscopy of cytospins prepared from these cultures. The cultured cells were morphologically similar to mammalian and trout DCs. Migration assays determined that these cells have the ability to move towards pathogens and pathogen associated molecular patterns, with a preference for peptidoglycans over lipopolysaccharides. The cells were also strongly phagocytic, engulfing bacteria and rapidly breaking them down. Barramundi DCs induced significant proliferation of responder populations of T-lymphocytes, supporting their role as antigen presenting cells. DC-SCRIPT expression in head kidney was higher 6 and 24 h following intraperitoneal challenge with peptidoglycan and lipopolysaccharide and declined after 3 days relative to PBS-injected controls. Relative expression was also lower in the spleen at 3 days post challenge but increased again at 7 days. As DC-SCRIPT is a constitutively expressed nuclear receptor, independent of immune activation, this may indicate initial migration of immature DCs from head kidney and spleen to the injection site, followed by return to the spleen for maturation and antigen presentation. DC-SCRIPT may be a valuable tool in the investigation of antigen presentation in fish and facilitate optimisation of vaccines and adjuvants for aquaculture.

摘要

抗原呈递是连接先天免疫识别和特异性免疫记忆的关键步骤。在哺乳动物中,这一过程由淋巴系统中的树突状细胞(DCs)精心协调,这些细胞启动抗原特异性淋巴细胞的克隆增殖。然而,鱼类缺乏经典的淋巴系统,目前也没有鱼类DCs的细胞标志物,因此对鱼类的抗原呈递了解甚少。最近,在包括虹鳟(Oncorhynchus mykiss)和斑马鱼(Danio rerio)在内的各种鱼类中,发现了结构和功能与哺乳动物DCs相似的抗原呈递细胞。本研究旨在确定鱼类DCs的潜在分子标志物,因此将目标锁定在DC-SCRIPT上,这是一种高度保守的锌指蛋白,在人类DCs的所有亚型中优先表达。通过脾脏和前肾来源的单核细胞成熟培养获得推定的树突状细胞。通过RACE PCR和基因组步移同源性在尖吻鲈中鉴定出DC-SCRIPT。通过Stellaris mRNA FISH在尖吻鲈细胞中检测到DC-SCRIPT的特异性表达,并结合暴露于细菌衍生肽聚糖时的MHCII表达,表明尖吻鲈中存在DCs。此外,通过对这些培养物制备的细胞涂片进行光学显微镜观察实现了形态学鉴定。培养的细胞在形态上与哺乳动物和鳟鱼的DCs相似。迁移试验确定这些细胞有能力向病原体和病原体相关分子模式移动,对肽聚糖的偏好超过脂多糖。这些细胞还具有强烈的吞噬作用,能吞噬细菌并迅速将其分解。尖吻鲈DCs诱导T淋巴细胞应答群体显著增殖,支持了它们作为抗原呈递细胞的作用。在用肽聚糖和脂多糖腹腔注射后6小时和24小时,尖吻鲈头肾中的DC-SCRIPT表达较高,相对于注射PBS的对照组,3天后表达下降。攻击后3天脾脏中的相对表达也较低,但在7天时再次升高。由于DC-SCRIPT是一种组成性表达的核受体,独立于免疫激活,这可能表明未成熟的DCs从头肾和脾脏最初迁移到注射部位,随后返回脾脏进行成熟和抗原呈递。DC-SCRIPT可能是研究鱼类抗原呈递的有价值工具,并有助于优化水产养殖疫苗和佐剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/641d/4501824/532a6b9cb835/pone.0132687.g001.jpg

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