Salzman Nita H, Underwood Mark A, Bevins Charles L
Department of Pediatrics, Division of Gastroenterology, The Medical College of Wisconsin, 8701 Watertown Plank Rd. Milwaukee, WI 53226, USA.
Semin Immunol. 2007 Apr;19(2):70-83. doi: 10.1016/j.smim.2007.04.002. Epub 2007 May 7.
Mucosal surfaces are colonized by a diverse and dynamic microbiota. Much investigation has focused on bacterial colonization of the intestine, home to the vast majority of this microbiota. Experimental evidence has highlighted that these colonizing microbes are essential to host development and homeostasis, but less is known about host factors that may regulate the composition of this ecosystem. While evidence shows that IgA has a role in shaping this microbiota, it is likely that effector molecules of the innate immune system are also involved. One hypothesis is that gene-encoded antimicrobial peptides, key elements of innate immunity throughout nature, have an essential role in this regulation. These effector molecules characteristically have activity against a broad spectrum of bacteria and other microbes. At mucosal surfaces, antimicrobial peptides may affect the numbers and/or composition of the colonizing microbiota. In humans and other mammals, defensins are a predominant class of antimicrobial peptides. In the small intestine, Paneth cells (specialized secretory epithelial cells) produce high quantities of defensins and several other antibiotic peptides and proteins. Data from murine models indicate that Paneth cell defensins play a pivotal role in defense from food and water-borne pathogens in the intestinal lumen. Recent studies in humans provide evidence that reduced Paneth cell defensin expression may be a key pathogenic factor in ileal Crohn's disease, a subgroup of inflammatory bowel disease (IBD), and changes in the colonizing microbiota may mediate this pathogenic mechanism. It is also possible that low levels of Paneth cell defensins, characteristic of normal intestinal development, may predispose premature neonates to necrotizing enterocolitis (NEC) through similar close links with the composition of the intestinal microbiota. Future studies to further define mechanisms by which defensins and other host factors regulate the composition of the intestinal microbiota will likely provide new insights into intestinal homeostasis and new therapeutic strategies for inflammatory and infectious diseases of the bowel.
黏膜表面定植着多样且动态变化的微生物群。大量研究聚焦于肠道的细菌定植,肠道是绝大多数此类微生物群的家园。实验证据表明,这些定植微生物对宿主发育和体内平衡至关重要,但对于可能调节这个生态系统组成的宿主因素却知之甚少。虽然有证据表明IgA在塑造这种微生物群方面发挥作用,但先天免疫系统的效应分子可能也参与其中。一种假说认为,基因编码的抗菌肽作为自然界中先天免疫的关键要素,在这种调节中起着至关重要的作用。这些效应分子通常对广谱细菌和其他微生物具有活性。在黏膜表面,抗菌肽可能会影响定植微生物群的数量和/或组成。在人类和其他哺乳动物中,防御素是一类主要的抗菌肽。在小肠中,潘氏细胞(专门的分泌上皮细胞)会产生大量的防御素以及其他几种抗生素肽和蛋白质。来自小鼠模型的数据表明,潘氏细胞防御素在抵御肠腔内食源和水源性病原体方面发挥着关键作用。最近在人类中的研究提供了证据,表明潘氏细胞防御素表达降低可能是回肠克罗恩病(炎症性肠病(IBD)的一个亚组)的关键致病因素,而定植微生物群的变化可能介导了这种致病机制。正常肠道发育所特有的低水平潘氏细胞防御素也有可能通过与肠道微生物群组成的类似紧密联系,使早产儿易患坏死性小肠结肠炎(NEC)。未来进一步明确防御素和其他宿主因素调节肠道微生物群组成机制的研究,可能会为肠道内平衡以及肠道炎症和感染性疾病的新治疗策略提供新的见解。