果蝇细胞因子 GBP2 通过 GPCR 受体 Mthl10 发挥免疫反应并调节 GBP1 的表达

IF 3.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Insect Biochemistry and Molecular Biology Pub Date : 2024-01-29 DOI:10.1016/j.ibmb.2024.104086
Masaya Ono , Takashi Matsumura , Eui Jae Sung , Takashi Koyama , Masanori Ochiai , Stephen B. Shears , Yoichi Hayakawa
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引用次数: 0

摘要

生长受阻肽(GBP)是一种昆虫细胞因子,最早发现于军蝽(Mythimna separata)。在同一物种中还发现了 GBP 的功能类似物--应激反应肽(SRP)。SRP基因的表达也被证明能被GBP增强,这表明这两种细胞因子都是在一个分级调控网络中组织起来的。虽然在黑腹果蝇中发现了 GBP1(CG15917)和 GBP2(CG11395),但只有 GBP1 的免疫功能得到了表征。 两种结构相似的肽的生物反应应该是协调的,但这方面的信息很少。在这里,我们证明了 GBP2 复制了果蝇 S2 细胞中 GBP1 介导的细胞免疫反应。此外,用靶向 GBP 受体基因 Mthl10 的 dsRNA 进行预处理可抑制 GBP2 诱导的反应。此外,用 GBP2 处理 S2 细胞可提高 GBP1 的表达水平,但 GBP1 并不影响 GBP2 的表达。在GBP1存在的情况下,GBP2衍生的GBP1表达增强并没有被观察到,这表明GBP2是GBP1/GBP2细胞因子网络的上游表达调节因子。在 Mthl10 敲除的细胞中没有观察到 GBP2 诱导的 GBP1 表达增强。在热应激条件下,果蝇幼虫和S2细胞中都观察到了GBP2表达的增强;在Mthl10敲除细胞和幼虫中,GBP1和GBP2表达的增强都被消除了。最后,在表达GCaMP3的S2细胞中进行的Ca2+动员试验表明,GBP2在Mthl10的上游动员Ca2+。我们的发现揭示了果蝇GBP1和GBP2通过一个分层的细胞因子网络控制免疫反应及其自身的表达水平,表明果蝇GBP1/GBP2系统可以作为一个简单的模型,用于研究相关细胞因子复合物的详细调控机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Drosophila cytokine GBP2 exerts immune responses and regulates GBP1 expression through GPCR receptor Mthl10

Growth-blocking peptide (GBP), an insect cytokine, was first found in armyworm Mythimna separata. A functional analogue of GBP, stress-responsive peptide (SRP), was also identified in the same species. SRP gene expression has been demonstrated to be enhanced by GBP, indicating that both cytokines are organized within a hierarchical regulatory network. Although GBP1 (CG15917) and GBP2 (CG11395) have been identified in Drosophila melanogaster, immunological functions have only been characterized for GBP1. It is expected that the biological responses of two structurally similar peptides should be coordinated, but there is little information on this topic. Here, we demonstrate that GBP2 replicates the GBP1-mediated cellular immune response from Drosophila S2 cells. Moreover, the GBP2-induced response was silenced by pre-treatment with dsRNA targeting the GBP receptor gene, Mthl10. Furthermore, treatment of S2 cells with GBP2 enhanced GBP1 expression levels, but GBP1 did not affect GBP2 expression. GBP2 derived enhancement of GBP1 expression was not observed in the presence of GBP1, indicating that GBP2 is an upstream expressional regulator of a GBP1/GBP2 cytokine network. GBP2-induced enhancement of GBP1 expression was not observed in Mthl10 knockdown cells. Enhancement of GBP2 expression was observed in both Drosophila larvae and S2 cells under heat stress conditions; expressional enhancement of both GBP1 and GBP2 was eliminated in Mthl10 knockdown cells and larvae. Finally, Ca2+ mobilization assay in GCaMP3-expressing S2 cells demonstrated that GBP2 mobilizes Ca2+ upstream of Mthl10. Our finding revealed that Drosophila GBP1 and GBP2 control immune responses as well as their own expression levels through a hierarchical cytokine network, indicating that Drosophila GBP1/GBP2 system can be a simple model that is useful to investigate the detailed regulatory mechanism of related cytokine complexes.

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来源期刊
CiteScore
7.40
自引率
5.30%
发文量
105
审稿时长
40 days
期刊介绍: This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.
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Identification of a gene promoter active in Lucilia sericata larval salivary glands using a rapid transient expression assay. In vivo RNAi screening identifies multiple deubiquitinases required for the maintenance of intestinal homeostasis in Drosophila. JAK and STAT5B mediate olfactory response of migratory locusts to their own volatiles. Functional redundancy of the three insulin receptors of cockroaches. Editorial Board
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