Department of Internal Medicine I, Robert Bosch Hospital, Stuttgart, Germany.
J Crohns Colitis. 2012 May;6(4):425-34. doi: 10.1016/j.crohns.2011.09.013. Epub 2011 Nov 15.
Olfactomedin-4 (OLFM4) is a glycoprotein characteristic of intestinal stem cells and apparently involved in mucosal defense of the stomach and colon. Here we studied its expression, regulation and function in IBD.
The expression of OLFM4, mucins Muc1 and Muc2, the goblet cell differentiation factor Hath1 and the proinflammatory cytokine IL-8 was measured in inflamed or noninflamed colon in IBD patients and controls. OLFM4 protein was located by immunohistochemistry, quantified by Dot Blot and its binding capacity to defensins HBD1-3 was investigated. The influence of bacteria with or without the Notch blocker dibenzazepine (DBZ) and of several cytokines on OLFM4 expression was determined in LS174T cells.
OLFM4 mRNA and protein were significantly upregulated in inflamed CD (4.3 and 1.7-fold) and even more pronounced in UC (24.8 and 3.7-fold). OLFM4 expression was correlated to IL-8 but not to Hath1. In controls immunostaining was restricted to the lower crypts but in inflamed IBD it expanded up to the epithelial surface including the mucus. OLFM4 bound to HBD1-3 without profoundly inactivating these defensins. In LS174T-cells OLFM4 mRNA was significantly augmented after incubation with Escherichia coli K12, Escherichia coli Nissle and Bacteroides vulgatus. DBZ downregulated OLFM4 expression and blocked bacterial induction whereas IL-22 but not TNF-α was stimulatory.
OLFM4 is overexpressed in active IBD and secreted into mucus. The induction is triggered by bacteria through the Notch pathway and also by the cytokine IL-22. OLFM4 seems to be of functional relevance in IBD as a mucus component, possibly by binding defensins.
嗅觉钙黏蛋白-4(OLFM4)是一种糖蛋白,其特征是存在于肠干细胞中,显然参与胃和结肠的黏膜防御。在这里,我们研究了它在 IBD 中的表达、调节和功能。
在 IBD 患者和对照者的炎症或非炎症结肠中测量 OLFM4、粘蛋白 Muc1 和 Muc2、杯状细胞分化因子 Hath1 和前炎症细胞因子 IL-8 的表达。通过免疫组织化学定位 OLFM4 蛋白,通过 Dot Blot 定量其与防御素 HBD1-3 的结合能力,并在 LS174T 细胞中研究有无 Notch 阻断剂地昔帕明(DBZ)的细菌以及几种细胞因子对 OLFM4 表达的影响。
OLFM4 mRNA 和蛋白在炎症性 CD(分别上调 4.3 和 1.7 倍)和 UC 中(分别上调 24.8 和 3.7 倍)显著上调。OLFM4 表达与 IL-8 相关,但与 Hath1 不相关。在对照者中,免疫染色仅限于下部隐窝,但在炎症性 IBD 中,其扩展到包括黏液在内的上皮表面。OLFM4 结合 HBD1-3 而不显著失活这些防御素。在 LS174T 细胞中,用大肠杆菌 K12、大肠杆菌 Nissle 和普通拟杆菌孵育后,OLFM4 mRNA 显著增加。DBZ 下调 OLFM4 表达并阻断细菌诱导,而 IL-22 但不是 TNF-α 具有刺激作用。
OLFM4 在活动性 IBD 中过度表达并分泌到黏液中。诱导是通过细菌通过 Notch 途径以及细胞因子 IL-22 触发的。OLFM4 似乎在 IBD 中具有作为黏液成分的功能相关性,可能通过结合防御素。