{"title":"家蚕C型凝集素5。","authors":"Yan-Xia Sun, Bang-Xian Zhang, Fang-Fang Liu, Xiang-Jun Rao","doi":"10.1093/jee/toad142","DOIUrl":null,"url":null,"abstract":"<p><p>C-type lectins (CTLs) are an important family of pattern recognition receptors (PRRs) that regulate immune responses. The CTL5 gene of the silkworm Bombyx mori L. (Lepidoptera: Bombycidae) encodes a protein comprised of 223 amino acids, containing a signal peptide and a carbohydrate recognition domain (CRD). Our previous study showed that CTL5 can facilitate the clearance of bacteria from larval hemocoel but the underlying mechanisms are unclear. In this study, we found that CTL5 was mainly expressed in fourth-instar larvae, adult moths, and the larval epidermis. CTL5 expression showed differential responses to both pathogenic stimuli and the molting hormone 20-hydroxyecdysone. The full-length (FL) and truncated (ΔN/ΔC/ΔNC) CTL5 recombinant proteins can bind to hemocytes, polysaccharides, bacteria, and spores of the entomopathogenic fungus Beauveria bassiana. Yeast 2-hybrid assays showed that the recombinant proteins can interact with integrin β2-β5 subunits. Recombinant proteins increased the phagocytic rate of hemocytes. Injection of recombinant CTL5 stimulated the expression of many immune genes in hemocytes, mainly antimicrobial peptides and immune signaling molecules. Additionally, transcriptomic sequencing of CTL5-stimulated hemocytes revealed 265 upregulated and 580 downregulated genes. Functional enrichment and the gene set enrichment analyses showed that differentially expressed genes were mainly enriched in innate immune responses and signaling. Our study suggests that CTL5 may act as an opsonin to enhance the clearance of pathogens by regulating both humoral and cellular responses.</p>","PeriodicalId":15632,"journal":{"name":"Journal of Economic Entomology","volume":" ","pages":"1862-1875"},"PeriodicalIF":2.2000,"publicationDate":"2023-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Functional characterization of Bombyx mori (Lepidoptera: Bombycidae) C-type lectin 5.\",\"authors\":\"Yan-Xia Sun, Bang-Xian Zhang, Fang-Fang Liu, Xiang-Jun Rao\",\"doi\":\"10.1093/jee/toad142\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>C-type lectins (CTLs) are an important family of pattern recognition receptors (PRRs) that regulate immune responses. The CTL5 gene of the silkworm Bombyx mori L. (Lepidoptera: Bombycidae) encodes a protein comprised of 223 amino acids, containing a signal peptide and a carbohydrate recognition domain (CRD). Our previous study showed that CTL5 can facilitate the clearance of bacteria from larval hemocoel but the underlying mechanisms are unclear. In this study, we found that CTL5 was mainly expressed in fourth-instar larvae, adult moths, and the larval epidermis. CTL5 expression showed differential responses to both pathogenic stimuli and the molting hormone 20-hydroxyecdysone. The full-length (FL) and truncated (ΔN/ΔC/ΔNC) CTL5 recombinant proteins can bind to hemocytes, polysaccharides, bacteria, and spores of the entomopathogenic fungus Beauveria bassiana. Yeast 2-hybrid assays showed that the recombinant proteins can interact with integrin β2-β5 subunits. Recombinant proteins increased the phagocytic rate of hemocytes. Injection of recombinant CTL5 stimulated the expression of many immune genes in hemocytes, mainly antimicrobial peptides and immune signaling molecules. Additionally, transcriptomic sequencing of CTL5-stimulated hemocytes revealed 265 upregulated and 580 downregulated genes. Functional enrichment and the gene set enrichment analyses showed that differentially expressed genes were mainly enriched in innate immune responses and signaling. 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引用次数: 0
摘要
C型凝集素(CTL)是调节免疫反应的一个重要的模式识别受体家族。家蚕Bombyx mori L.(鳞翅目:Bombycidae)的CTL5基因编码一种由223个氨基酸组成的蛋白质,包含一个信号肽和一个碳水化合物识别结构域(CRD)。我们之前的研究表明,CTL5可以促进幼虫血腔中细菌的清除,但其潜在机制尚不清楚。在本研究中,我们发现CTL5主要在四龄幼虫、成虫和幼虫表皮中表达。CTL5表达对致病性刺激和蜕皮激素20-羟基蜕皮激素均表现出不同的反应。全长(FL)和截短(ΔN/ΔC/ΔNC)CTL5重组蛋白可以与昆虫病原真菌白僵菌的血细胞、多糖、细菌和孢子结合。酵母双杂交分析表明,重组蛋白可以与整合素β2-β5亚基相互作用。重组蛋白提高了血细胞的吞噬率。注射重组CTL5刺激了血细胞中许多免疫基因的表达,主要是抗菌肽和免疫信号分子。此外,CTL5刺激的血细胞的转录组测序显示265个上调基因和580个下调基因。功能富集和基因集富集分析表明,差异表达基因主要富集在先天免疫反应和信号传导中。我们的研究表明,CTL5可能作为一种调理素,通过调节体液和细胞反应来增强病原体的清除。
Functional characterization of Bombyx mori (Lepidoptera: Bombycidae) C-type lectin 5.
C-type lectins (CTLs) are an important family of pattern recognition receptors (PRRs) that regulate immune responses. The CTL5 gene of the silkworm Bombyx mori L. (Lepidoptera: Bombycidae) encodes a protein comprised of 223 amino acids, containing a signal peptide and a carbohydrate recognition domain (CRD). Our previous study showed that CTL5 can facilitate the clearance of bacteria from larval hemocoel but the underlying mechanisms are unclear. In this study, we found that CTL5 was mainly expressed in fourth-instar larvae, adult moths, and the larval epidermis. CTL5 expression showed differential responses to both pathogenic stimuli and the molting hormone 20-hydroxyecdysone. The full-length (FL) and truncated (ΔN/ΔC/ΔNC) CTL5 recombinant proteins can bind to hemocytes, polysaccharides, bacteria, and spores of the entomopathogenic fungus Beauveria bassiana. Yeast 2-hybrid assays showed that the recombinant proteins can interact with integrin β2-β5 subunits. Recombinant proteins increased the phagocytic rate of hemocytes. Injection of recombinant CTL5 stimulated the expression of many immune genes in hemocytes, mainly antimicrobial peptides and immune signaling molecules. Additionally, transcriptomic sequencing of CTL5-stimulated hemocytes revealed 265 upregulated and 580 downregulated genes. Functional enrichment and the gene set enrichment analyses showed that differentially expressed genes were mainly enriched in innate immune responses and signaling. Our study suggests that CTL5 may act as an opsonin to enhance the clearance of pathogens by regulating both humoral and cellular responses.
期刊介绍:
Journal of Economic Entomology the most-cited entomological journal – publishes articles on the economic significance of insects and other arthropods and includes sections on apiculture & social insects, insecticides, biological control, household & structural insects, crop protection, forest entomology, and more. In addition to research papers, Journal of Economic Entomology publishes Reviews, interpretive articles in a Forum section, Short Communications, and Letters to the Editor. The journal is published bimonthly in February, April, June, August, October, and December.