A self-marker-like protein governs hemocyte allorecognition in Halocynthia roretzi.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Accounts of Chemical Research Pub Date : 2019-12-16 eCollection Date: 2019-01-01 DOI:10.1186/s40851-019-0149-8
Masaki Ema, Taizo Okada, Miki Takahashi, Masato Uchiyama, Hideo Kubo, Hideaki Moriyama, Hitoshi Miyakawa, Midori Matsumoto
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引用次数: 0

Abstract

Background: Self-incompatibility, fusion/non-fusion reactions, and contact reactions (CRs) have all been identified as allorecognition phenomena in ascidians. CR is a reaction characteristic of the hemocytes of Halocynthia roretzi, whereby they release phenol oxidase (PO) upon contact with non-self hemocytes. Thus, these cells may represent a primitive form of the vertebrate immune system. In the present study, we focused on the CR of H. roretzi hemocytes and sought to identify self-marker proteins that distinguish between self and non-self cells.

Results: We initially generated a CR-inducing monoclonal antibody against the complete hemocyte membrane-protein complement (mAb11B16B10). This antibody was identified based on the differential induction of PO activity in individual organisms. The level of PO activity induced by this antibody in individual ascidians was consistent with the observed CR-induced PO activity. mAb11B16B10 recognized a series of 12 spots corresponding to a 100-kDa protein, with differing isoelectric points (pIs). A comparison of the 2D electrophoresis gels of samples from CR-reactive/non-reactive individuals revealed that some spots in this series in hemocytes were common to the CR-non-inducible individuals, but not to CR-inducible individuals. We cloned the corresponding gene and named it Halocynthia roretzi self-marker-like protein-1 (HrSMLP1). This gene is similar to the glycoprotein DD3-3 found in Dictyostelium, and is conserved in invertebrates.

Conclusion: We generated a CR-inducing monoclonal antibody (mAb11B16B10) that recognized a series of novel membrane proteins (HrSMLP1) in the hemocytes of H. roretzi. The combination of expressed spots of HrSMLP1 distinguishes non-self cells from self cells with respect to CR inducibility. Given that the HrSMLP1 gene is a single gene, it may represent a novel type of self-marker protein with a role in CR.

Abstract Image

Abstract Image

Abstract Image

Halocynthia roretzi 的一种自我标记样蛋白控制着血细胞的异源识别。
背景:自相容性、融合/非融合反应和接触反应(CRs)都被认为是腹足类的异源识别现象。接触反应(CR)是 Halocynthia roretzi 的血细胞特有的一种反应,当它们与非自体血细胞接触时会释放酚氧化酶(PO)。因此,这些细胞可能代表了脊椎动物免疫系统的一种原始形式。在本研究中,我们重点研究了姬蛙血球细胞的CR,并试图找出区分自体细胞和非自体细胞的自体标记蛋白:结果:我们最初生成了一种针对完整血球细胞膜蛋白补体的 CR 诱导型单克隆抗体(mAb11B16B10)。这种抗体是根据在不同生物体中诱导 PO 活性的差异而确定的。mAb11B16B10 能识别一系列 12 个等电点(pIs)不同的 100 kDa 蛋白点。通过比较 CR 反应个体和非反应个体样本的二维电泳凝胶,我们发现血细胞中这一系列斑点中的某些斑点在 CR 非诱导个体中是常见的,但在 CR 诱导个体中却不常见。我们克隆了相应的基因,并将其命名为Halocynthia roretzi self-marker-like protein-1(HrSMLP1)。该基因与竹荪中的糖蛋白DD3-3相似,在无脊椎动物中也是保守的:我们产生了一种可诱导 CR 的单克隆抗体(mAb11B16B10),该抗体可识别 H. roretzi 血细胞中的一系列新型膜蛋白(HrSMLP1)。在 CR 诱导性方面,HrSMLP1 的表达点组合可将非自体细胞与自体细胞区分开来。鉴于 HrSMLP1 基因是一个单基因,它可能代表了一种在 CR 中发挥作用的新型自我标记蛋白。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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