Shrestha Archana, Robertson Susan L, Garcia Jorge, Beingasser Juliann, McClane Bruce A, Uzal Francisco A
Department of Microbiology and Molecular Genetics, University of Pittsburgh, School of Medicine, Pittsburgh, Pennsylvania, USA.
California Animal Health and Food Safety Laboratory System, School of Veterinary Medicine, University of California, Davis, San Bernardino, California, USA.
Infect Immun. 2014 Nov;82(11):4778-88. doi: 10.1128/IAI.02453-14. Epub 2014 Aug 25.
Clostridium perfringens enterotoxin (CPE) action starts when the toxin binds to claudin receptors. Claudins contain two extracellular loop domains, with the second loop (ECL-2) being slightly smaller than the first. CPE has been shown to bind to ECL-2 in receptor claudins. We recently demonstrated that Caco-2 cells (a naturally CPE-sensitive enterocyte-like cell line) can be protected from CPE-induced cytotoxicity by preincubating the enterotoxin with soluble full-length recombinant claudin-4 (rclaudin-4), which is a CPE receptor, but not with recombinant nonreceptor claudins, such as rclaudin-1. The current study evaluated whether a synthetic peptide corresponding to the claudin-4 ECL-2 sequence can similarly inhibit CPE action in vitro and in vivo. Significant protection of Caco-2 cells was also observed using either rclaudin-4 or the claudin-4 ECL-2 peptide in both a preincubation assay and a coincubation assay. This inhibitory effect was specific, since rclaudin-1 and a synthetic peptide based on the claudin-1 ECL-2 offered no protection to Caco-2 cells. However, the claudin-4 ECL-2 peptide was unable to neutralize cytotoxicity if CPE had already bound to Caco-2 cells. When the study was repeated in vivo using a rabbit small intestinal loop assay, preincubation or coincubation of CPE with the claudin-4 ECL-2 peptide significantly and specifically inhibited the development of CPE-induced luminal fluid accumulation and histologic lesions in rabbit small intestinal loops. No similar in vivo protection from CPE was afforded by the claudin-1 ECL-2 peptide. These results suggest that claudin-4 ECL-2 peptides should be further investigated for their potential therapeutic application against CPE-associated disease.
产气荚膜梭菌肠毒素(CPE)的作用始于该毒素与紧密连接蛋白受体结合之时。紧密连接蛋白含有两个细胞外环结构域,第二个环(ECL-2)比第一个略小。已证明CPE与受体紧密连接蛋白中的ECL-2结合。我们最近证明,通过将肠毒素与可溶性全长重组紧密连接蛋白-4(rclaudin-4,一种CPE受体)预孵育,可保护Caco-2细胞(一种天然对CPE敏感的肠上皮样细胞系)免受CPE诱导的细胞毒性,但与重组非受体紧密连接蛋白(如rclaudin-1)预孵育则无此效果。本研究评估了与紧密连接蛋白-4 ECL-2序列相对应的合成肽是否能在体外和体内类似地抑制CPE的作用。在预孵育试验和共孵育试验中,使用rclaudin-4或紧密连接蛋白-4 ECL-2肽均观察到对Caco-2细胞有显著保护作用。这种抑制作用具有特异性,因为rclaudin-1和基于紧密连接蛋白-1 ECL-2的合成肽对Caco-2细胞无保护作用。然而,如果CPE已经与Caco-2细胞结合,紧密连接蛋白-4 ECL-2肽则无法中和细胞毒性。当使用兔小肠袢试验在体内重复该研究时,CPE与紧密连接蛋白-4 ECL-2肽预孵育或共孵育可显著且特异性地抑制兔小肠袢中CPE诱导的管腔液积聚和组织学损伤的发展。紧密连接蛋白-1 ECL-2肽在体内未对CPE提供类似的保护。这些结果表明,紧密连接蛋白-4 ECL-2肽在抗CPE相关疾病的潜在治疗应用方面应进一步研究。