Department of Biochemistry, Kansas State University, Manhattan, KS 66506, USA.
FEBS J. 2010 Jan;277(1):148-62. doi: 10.1111/j.1742-4658.2009.07465.x. Epub 2009 Nov 26.
The innate immune response of insects includes induced expression of genes encoding a variety of antimicrobial peptides. The signaling pathways that stimulate this gene expression have been well characterized by genetic analysis in Drosophila melanogaster, but are not well understood in most other insect species. One such pathway involves proteolytic activation of a cytokine called Spätzle, which functions in dorsal-ventral patterning in early embryonic development and in the antimicrobial immune response in larvae and adults. We have investigated the function of Spätzle in a lepidopteran insect, Manduca sexta, in which hemolymph proteinases activated during immune responses have been characterized biochemically. Two cDNA isoforms for M. sexta Spätzle-1 differ because of alternative splicing, resulting in a 10 amino acid residue insertion in the pro-region of proSpätzle-1B that is not present in proSpätzle-1A. The proSpätzle-1A cDNA encodes a 32.7 kDa polypeptide that is 23% and 44% identical to D. melanogaster and Bombyx mori Spätzle-1, respectively. Recombinant proSpätzle-1A was a disulfide-linked homodimer. M. sexta hemolymph proteinase 8 cleaved proSpätzle-1A to release Spätzle-C108, a dimer of the C-terminal 108 residue cystine-knot domain. Injection of Spätzle-C108, but not proSpätzle-1A, into larvae stimulated expression of several antimicrobial peptides and proteins, including attacin-1, cecropin-6, moricin, lysozyme, and the immunoglobulin domain protein hemolin, but did not significantly affect the expression of two bacteria-inducible pattern recognition proteins, immulectin-2 and beta-1,3-glucan recognition protein-2. The results of this and other recent studies support a model for a pathway in which the clip-domain proteinase pro-hemolymph proteinase 6 becomes activated in plasma upon exposure to Gram-negative or Gram-positive bacteria or to beta-1,3-glucan. Hemolymph proteinase 6 then activates pro-hemolymph proteinase 8, which in turn activates Spätzle-1. The resulting Spätzle-C108 dimer is likely to function as a ligand to activate a Toll pathway in M. sexta as a response to a wide variety of microbial challenges, stimulating a broad response to infection. Structured digital abstract * MINT-7295125: Spätzle 1A (uniprotkb:C8BMD1) and Spätzle 1A (uniprotkb:C8BMD1) bind (MI:0407) by comigration in gel electrophoresis (MI:0807).
昆虫的先天免疫反应包括诱导多种抗菌肽基因的表达。在黑腹果蝇(Drosophila melanogaster)中,通过遗传分析已经很好地描述了刺激这种基因表达的信号通路,但在大多数其他昆虫物种中还没有很好地理解。其中一条途径涉及细胞因子 Spätzle 的蛋白水解激活,它在早期胚胎发育中的背腹模式形成和幼虫及成虫的抗菌免疫反应中起作用。我们研究了 Spätzle 在鳞翅目昆虫 Manduca sexta 中的功能,在该昆虫中,免疫反应中激活的血淋巴蛋白酶已通过生化方法进行了表征。两种 cDNA 异构体 M. sexta Spätzle-1 的差异在于选择性剪接,导致 proSpätzle-1B 的前区插入 10 个氨基酸残基,而 proSpätzle-1A 中不存在。proSpätzle-1A cDNA 编码一个 32.7 kDa 的多肽,分别与黑腹果蝇和家蚕 Spätzle-1 有 23%和 44%的同一性。重组 proSpätzle-1A 是一个二硫键连接的同源二聚体。M. sexta 血淋巴蛋白酶 8 切割 proSpätzle-1A 释放 Spätzle-C108,这是 C 末端 108 残基胱氨酸结结构域的二聚体。注射 Spätzle-C108(而非 proSpätzle-1A)到幼虫中可刺激几种抗菌肽和蛋白的表达,包括 attacin-1、cecropin-6、moricin、溶菌酶和免疫球蛋白域蛋白 hemolin,但对两种细菌诱导的模式识别蛋白 immulectin-2 和β-1,3-葡聚糖识别蛋白-2 的表达没有显著影响。本研究和其他最近的研究结果支持这样一种模型,即剪接体蛋白水解酶 pro-hemolymph 蛋白酶 6 在暴露于革兰氏阴性或革兰氏阳性细菌或β-1,3-葡聚糖时在血浆中被激活。血淋巴蛋白酶 6 然后激活 pro-hemolymph 蛋白酶 8,后者又激活 Spätzle-1。产生的 Spätzle-C108 二聚体可能作为配体发挥作用,激活 M. sexta 中的 Toll 途径,以响应各种微生物挑战,从而对感染产生广泛的反应。