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血吸虫食道腺:血液处理的启动者。

The schistosome oesophageal gland: initiator of blood processing.

机构信息

National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, Key Laboratory of Parasitology and Vector Biology, Ministry of Health, Shanghai, People's Republic of China.

出版信息

PLoS Negl Trop Dis. 2013 Jul 25;7(7):e2337. doi: 10.1371/journal.pntd.0002337. Print 2013.

Abstract

BACKGROUND

Although the ultrastructure of the schistosome esophageal gland was described >35 years ago, its role in the processing of ingested blood has never been established. The current study was prompted by our identification of MEG-4.1 expression in the gland and the observation of erythrocyte uncoating in the posterior esophagus.

METHODOLOGY/PRINCIPAL FINDINGS: The salient feature of the posterior esophagus, characterized by confocal and electron microscopy, is the enormous increase in membrane surface area provided by the plate-like extensions and basal invaginations of the lining syncytium, with unique crystalloid vesicles releasing their contents between the plates. The feeding process was shown by video microscopy to be divided into two phases, blood first accumulating in the anterior lumen before passing as a bolus to the posterior. There it streamed around a plug of material revealed by confocal microscopy as tethered leucocytes. These were present in far larger numbers than predicted from the volume of the lumen, and in varying states of damage and destruction. Intact erythrocytes were detected in the anterior esophagus but not observed thereafter, implying that their lysis occurred rapidly as they enter the posterior. Two further genes, MEGs 4.2 and 14, were shown to be expressed exclusively in the esophageal gland. Bioinformatics predicted that MEGs 4.1 and 4.2 possessed a common hydrophobic region with a shared motif, while antibodies to SjMEG-4.1 showed it was bound to leucocytes in the esophageal lumen. It was also predicted that MEGs 4.1 and 14 were heavily O-glycosylated and this was confirmed for the former by 2D-electrophoresis and Western blotting.

CONCLUSIONS/SIGNIFICANCE: The esophageal gland and its products play a central role in the processing of ingested blood. The binding of host antibodies in the esophageal lumen shows that some constituents are antibody targets and could provide a new source of vaccine candidates.

摘要

背景

尽管 35 多年前就已经描述了血吸虫食道腺的超微结构,但它在处理摄入的血液中的作用从未得到证实。本研究的起因是我们在腺体内鉴定出 MEG-4.1 的表达,并观察到后食道中的红细胞脱衣。

方法/主要发现:后食道的显著特征是由衬里合胞体的板状延伸和基底内陷提供的巨大膜表面积增加,通过共聚焦和电子显微镜观察到,具有独特的结晶状囊泡在板之间释放其内容物。通过视频显微镜观察到的摄食过程分为两个阶段,血液首先在前腔中积聚,然后作为一个团块向后腔传递。在后腔中,它围绕着一个由共聚焦显微镜显示为拴系白细胞的物质塞流动。这些白细胞的数量远远超过腔体积的预测值,并且处于不同的损伤和破坏状态。在前食道中检测到完整的红细胞,但此后未观察到,这表明它们在进入后食道时迅速溶解。另外两个基因,MEGs 4.2 和 14,被证明仅在食道腺中表达。生物信息学预测 MEGs 4.1 和 4.2 具有一个共同的疏水区,具有共享的基序,而针对 SjMEG-4.1 的抗体表明它与食道腔中的白细胞结合。还预测 MEGs 4.1 和 14 高度 O-糖基化,这在前者的 2D 电泳和 Western blot 中得到证实。

结论/意义:食道腺及其产物在摄入血液的处理中起核心作用。食道腔中宿主抗体的结合表明,某些成分是抗体靶标,可为疫苗候选物提供新的来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf85/3723592/f354b52c4abb/pntd.0002337.g001.jpg

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