Bacteria penetrate the normally impenetrable inner colon mucus layer in both murine colitis models and patients with ulcerative colitis

粘液 粘蛋白 结肠炎 溃疡性结肠炎 离体 上皮 粘蛋白2 病理 生物 微生物学 医学 体内 免疫学 生物化学 基因 基因表达 生物技术 疾病 生态学
作者
Malin Johansson,Jenny K. Gustafsson,Jessica Holmén‐Larsson,Karolina S. Jabbar,Lijun Xia,Hua Xu,Fayez K. Ghishan,Frédéric A. Carvalho,Andrew T. Gewirtz,Henrik Sjövall,Gunnar C. Hansson
出处
期刊:Gut [BMJ]
卷期号:63 (2): 281-291 被引量:851
标识
DOI:10.1136/gutjnl-2012-303207
摘要

Objective

The inner mucus layer in mouse colon normally separates bacteria from the epithelium. Do humans have a similar inner mucus layer and are defects in this mucus layer a common denominator for spontaneous colitis in mice models and ulcerative colitis (UC)?

Methods and results

The colon mucus layer from mice deficient in Muc2 mucin, Core 1 O-glycans, Tlr5, interleukin 10 (IL-10) and Slc9a3 (Nhe3) together with that from dextran sodium sulfate-treated mice was immunostained for Muc2, and bacterial localisation in the mucus was analysed. All murine colitis models revealed bacteria in contact with the epithelium. Additional analysis of the less inflamed IL-10−/− mice revealed a thicker mucus layer than wild-type, but the properties were different, as the inner mucus layer could be penetrated both by bacteria in vivo and by fluorescent beads the size of bacteria ex vivo. Clear separation between bacteria or fluorescent beads and the epithelium mediated by the inner mucus layer was also evident in normal human sigmoid colon biopsy samples. In contrast, mucus on colon biopsy specimens from patients with UC with acute inflammation was highly penetrable. Most patients with UC in remission had an impenetrable mucus layer similar to that of controls.

Conclusions

Normal human sigmoid colon has an inner mucus layer that is impenetrable to bacteria. The colon mucus in animal models that spontaneously develop colitis and in patients with active UC allows bacteria to penetrate and reach the epithelium. Thus colon mucus properties can be modulated, and this suggests a novel model of UC pathophysiology.
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