Wehkamp Jan, Chu Hiutung, Shen Bo, Feathers Ryan W, Kays Robert J, Lee Sarah K, Bevins Charles L
Department of Medical Microbiology and Immunology, School of Medicine, University of California at Davis, One Shields Avenue, Tupper Hall Room 3146, 95616-8645, USA.
FEBS Lett. 2006 Oct 2;580(22):5344-50. doi: 10.1016/j.febslet.2006.08.083. Epub 2006 Sep 12.
Antimicrobial peptides and proteins are key effectors of innate immunity, expressed both by circulating phagocytic cells and by epithelial cells of mucosal tissues. In the human small intestine, Paneth cells are secretory epithelial cells that express the antimicrobials human alpha-defensin-5 (HD5), HD6, lysozyme and secretory phospholipase A(2) (sPLA(2)), and recent studies have implicated reduced HD5 and HD6 expression levels in the pathogenesis of ileal Crohn's disease. However, expression levels of these molecules have not been determined routinely by techniques that readily permit quantitative comparisons of their distribution between tissues and samples. Using quantitative real-time PCR with external standards and Northern blot analysis, we compared expression levels of mRNA encoding these four Paneth cell antimicrobial peptides, as well as circulating human neutrophil defensins in several different gastrointestinal tissues and the bone marrow. HD5 and HD6 were the most abundant antimicrobials expressed in the small intestine. The concentration of HD5 mRNA is approximately 5 x 10(5) copies per 10ng RNA in the jejunum and ileum; HD6 mRNA levels were about six times lower than those of HD5. With the exception of low levels in the pancreas (10(3) copies/10 ng RNA), the expression of HD5 and HD6 in tissues other than small intestine was at or below detectable limits. The expression of sPLA2 and lysozyme mRNA was observed in the small intestine (approximately, 3 x 10(3) and 9 x 10(3) copies/10 ng RNA, respectively), but also in several other tissues. Lysozyme expression was high in the duodenum (10(5) copies/10 ng RNA), and the protein localized to both Brunner's glands in the lamina propria and Paneth cells. By comparison, the hematopoietic alpha-defensins HNP1-3 mRNA were detected at 6 x 10(5) copies per 10 ng RNA in the bone marrow. These quantitative RT-PCR data from healthy tissues represents the first quantitative topographical assessment of antimicrobial expression in the gastrointestinal tract and provides a means to directly compare expression levels between healthy tissues and disease specimens for multiple antimicrobial peptides.
抗菌肽和蛋白质是天然免疫的关键效应分子,由循环吞噬细胞和黏膜组织的上皮细胞表达。在人类小肠中,潘氏细胞是分泌性上皮细胞,表达抗菌物质人α-防御素-5(HD5)、HD6、溶菌酶和分泌型磷脂酶A2(sPLA2),最近的研究表明,HD5和HD6表达水平降低与回肠克罗恩病的发病机制有关。然而,这些分子的表达水平尚未通过能够轻松对其在组织和样本之间的分布进行定量比较的技术进行常规测定。我们使用带有外参的定量实时PCR和Northern印迹分析,比较了在几种不同的胃肠道组织和骨髓中,编码这四种潘氏细胞抗菌肽的mRNA以及循环中的人中性粒细胞防御素的表达水平。HD5和HD6是小肠中表达最丰富的抗菌物质。空肠和回肠中HD5 mRNA的浓度约为每10 ng RNA 5×10⁵拷贝;HD6 mRNA水平比HD5低约六倍。除胰腺中水平较低(10³拷贝/10 ng RNA)外,小肠以外组织中HD5和HD6的表达处于或低于可检测限。在小肠中观察到sPLA2和溶菌酶mRNA的表达(分别约为3×10³和9×10³拷贝/10 ng RNA),但在其他几种组织中也有表达。十二指肠中溶菌酶表达较高(10⁵拷贝/10 ng RNA),该蛋白定位于固有层的Brunner腺和潘氏细胞。相比之下,在骨髓中检测到造血α-防御素HNP1 - 3 mRNA的水平为每10 ng RNA 6×10⁵拷贝。这些来自健康组织的定量RT-PCR数据代表了胃肠道抗菌物质表达的首次定量拓扑评估,并提供了一种直接比较多种抗菌肽在健康组织和疾病标本之间表达水平的方法。