Goupil Louise S, Ivry Sam L, Hsieh Ivy, Suzuki Brian M, Craik Charles S, O'Donoghue Anthony J, McKerrow James H
Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, United States of America.
Department of Pathology, University of California, San Francisco, San Francisco, California, United States of America.
PLoS Negl Trop Dis. 2016 Aug 8;10(8):e0004893. doi: 10.1371/journal.pntd.0004893. eCollection 2016 Aug.
Proteases perform numerous vital functions in flatworms, many of which are likely to be conserved throughout the phylum Platyhelminthes. Within this phylum are several parasitic worms that are often poorly characterized due to their complex life-cycles and lack of responsiveness to genetic manipulation. The flatworm Schmidtea mediterranea, or planaria, is an ideal model organism to study the complex role of protein digestion due to its simple life cycle and amenability to techniques like RNA interference (RNAi). In this study, we were interested in deconvoluting the digestive protease system that exists in the planarian gut. To do this, we developed an alcohol-induced regurgitation technique to enrich for the gut enzymes in S. mediterranea. Using a panel of fluorescent substrates, we show that this treatment produces a sharp increase in proteolytic activity. These enzymes have broad yet diverse substrate specificity profiles. Proteomic analysis of the gut contents revealed the presence of cysteine and metallo-proteases. However, treatment with class-specific inhibitors showed that aspartyl and cysteine proteases are responsible for the majority of protein digestion. Specific RNAi knockdown of the cathepsin B-like cysteine protease (SmedCB) reduced protein degradation in vivo. Immunohistochemistry and whole-mount in situ hybridization (WISH) confirmed that the full-length and active forms of SmedCB are found in secretory cells surrounding the planaria intestinal lumen. Finally, we show that the knockdown of SmedCB reduces the speed of tissue regeneration. Defining the roles of proteases in planaria can provide insight to functions of conserved proteases in parasitic flatworms, potentially uncovering drug targets in parasites.
蛋白酶在扁形虫中发挥着众多重要功能,其中许多功能可能在整个扁形动物门中保守存在。在这个门中,有几种寄生蠕虫,由于其复杂的生命周期以及对基因操作缺乏反应性,其特征通常了解甚少。地中海涡虫(Schmidtea mediterranea),即涡虫,因其简单的生命周期以及对RNA干扰(RNAi)等技术的适应性,是研究蛋白质消化复杂作用的理想模式生物。在本研究中,我们感兴趣的是解析涡虫肠道中存在的消化蛋白酶系统。为此,我们开发了一种酒精诱导反流技术,以富集地中海涡虫的肠道酶。使用一组荧光底物,我们表明这种处理使蛋白水解活性急剧增加。这些酶具有广泛但多样的底物特异性谱。对肠道内容物的蛋白质组分析揭示了半胱氨酸和金属蛋白酶的存在。然而,用类别特异性抑制剂处理表明,天冬氨酸和半胱氨酸蛋白酶是蛋白质消化的主要原因。组织蛋白酶B样半胱氨酸蛋白酶(SmedCB)的特异性RNAi敲低降低了体内的蛋白质降解。免疫组织化学和全组织原位杂交(WISH)证实,在涡虫肠腔周围的分泌细胞中发现了全长和活性形式的SmedCB。最后,我们表明SmedCB的敲低降低了组织再生的速度。确定蛋白酶在涡虫中的作用可以深入了解寄生扁形虫中保守蛋白酶的功能,有可能揭示寄生虫中的药物靶点。