Heimesaat M M, Heilmann K, Kühl A A, Erben U, Rühl M, Fischer A, Farndale R W, Bereswill S, Göbel U B, Zeitz M, Somasundaram R, Freise C
Eur J Microbiol Immunol (Bp). 2012 Sep;2(3):192-200. doi: 10.1556/EuJMI.2.2012.3.4. Epub 2012 Sep 10.
In experimental models of and humans with intestinal inflammation, increased levels of the matrix-degrading gelatinases MMP-2 and -9 in inflamed tissues can be detected. The synthetic collagen analogue (Gly-Pro-Hyp)10, (GPO)10, has been identified as a relevant binding structure for proMMP-2/-9 and promotes enzymatic activity of proMMP-2. Since targeted MMP strategies might offer promising anti-inflammatory treatment options, we for the first time studied in vivo actions exerted by (GPO)10 applying an acute dextrane sulfate sodium (DSS) induced colitis model. Seven-day intraperitoneal (GPO)10 treatment ameliorated clinical symptoms and histopathological colonic changes as compared to placebo controls with severe colitis. (GPO)10-treated mice displayed a diminished influx of neutrophils, and T- and B-lymphocytes into their colonic mucosa whereas numbers of regulatory T-cells and regenerative cells were higher as compared to placebo controls. Furthermore, IL-6 secretion was down-regulated in ex vivo colonic biopsies derived from (GPO)10-treated mice whereas higher concentrations of the anti-inflammatory cytokine IL-10 in extra-intestinal compartments such as MLN and spleen could be detected. Strikingly, influx of inflammatory cells into lungs was abolished following (GPO)10 application. We therefore propose (GPO)10 as a promising effective and safe treatment option of intestinal and extra-intestinal inflammatory conditions in humans.
在肠道炎症的实验模型及人类患者中,可以检测到炎症组织中基质降解明胶酶MMP - 2和 - 9的水平升高。合成胶原蛋白类似物(Gly - Pro - Hyp)10,即(GPO)10,已被确定为proMMP - 2/-9的相关结合结构,并能促进proMMP - 2的酶活性。由于靶向MMP策略可能提供有前景的抗炎治疗选择,我们首次在急性硫酸葡聚糖钠(DSS)诱导的结肠炎模型中研究了(GPO)10的体内作用。与患有严重结肠炎的安慰剂对照组相比,为期7天的腹腔内(GPO)10治疗改善了临床症状和结肠组织病理学变化。(GPO)10治疗的小鼠结肠黏膜中中性粒细胞、T淋巴细胞和B淋巴细胞的浸润减少,而与安慰剂对照组相比,调节性T细胞和再生细胞的数量更高。此外,来自(GPO)10治疗小鼠的离体结肠活检组织中IL - 分泌下调,而在诸如肠系膜淋巴结和脾脏等肠外隔室中可检测到更高浓度的抗炎细胞因子IL - 10。引人注目的是,应用(GPO)10后炎症细胞向肺部的浸润被消除。因此,我们认为(GPO)10是一种有前景的、有效且安全的治疗人类肠道和肠外炎症性疾病的选择。