Medina Carlos, Santana Alfredo, Paz Maria Cristina, Díaz-Gonzalez Federico, Farre Esther, Salas Antonio, Radomski Marek W, Quintero Enriquie
Servicios de Gastroenterología y, Hospital Universitario de Canarias, La Laguna, Tenerife, Spain.
J Leukoc Biol. 2006 May;79(5):954-62. doi: 10.1189/jlb.1005544. Epub 2006 Feb 14.
Proteolysis and degradation of extracellular matrix by metalloproteinases (MMPs) may contribute to intestinal injury in inflammatory bowel disease. In the present study, we investigated the pathogenic role of gelatinases (MMP-9 and MMP-2) on transmural colonic injury in a rat model of chronic colitis, which was induced by intracolonic instillation of trinitrobenzene sulfonic acid (TNBS). The activity and expression of MMP-2 and MMP-9 were measured in colonic tissue and peripheral neutrophils by fluorescence, zymography, Western blot, or immunohistochemistry at different time-points. Furthermore, myeloperoxidase content in colonic homogenates was analyzed to evaluate inflammation. Finally, morphological changes were assessed following early or delayed administration of CGS-27023-A, a synthetic inhibitor of MMPs. We found that the induction of colitis led to a significant up-regulation in tissue gelatinase concentration, whereas no changes in collagenase activity were observed. In addition, up-regulation of pro-MMP-9, but not of pro-MMP-2, was found on Days 7 and 10 following the induction of colitis. Furthermore, transmural MMP-9 was detected by immunofluorescent staining in the inflamed tissue. Consistent with tissue samples, neutrophils from colitic rats showed a significantly increased activity of pro-MMP-9. Finally, early but not delayed treatment with CGS-27023-A attenuated colonic mucosal injury in rats with TNBS-induced colitis. In conclusion, up-regulation of MMP-9 in peripheral and colonic neutrophils modulates transmural colonic injury in rats with TNBS-induced colitis.
金属蛋白酶(MMPs)对细胞外基质的蛋白水解和降解可能在炎症性肠病的肠道损伤中起作用。在本研究中,我们在慢性结肠炎大鼠模型中,研究了明胶酶(MMP-9和MMP-2)对透壁性结肠损伤的致病作用,该模型由结肠内注入三硝基苯磺酸(TNBS)诱导。在不同时间点,通过荧光、酶谱分析、蛋白质印迹或免疫组织化学法测定结肠组织和外周中性粒细胞中MMP-2和MMP-9的活性及表达。此外,分析结肠匀浆中的髓过氧化物酶含量以评估炎症。最后,在早期或延迟给予MMPs的合成抑制剂CGS-27023-A后,评估形态学变化。我们发现,结肠炎的诱导导致组织明胶酶浓度显著上调,而未观察到胶原酶活性的变化。此外,在结肠炎诱导后的第7天和第10天,发现前MMP-9上调,而前MMP-2未上调。此外,通过免疫荧光染色在炎症组织中检测到透壁性MMP-9。与组织样本一致,来自结肠炎大鼠的中性粒细胞显示前MMP-9的活性显著增加。最后,早期而非延迟给予CGS-27023-A可减轻TNBS诱导的结肠炎大鼠的结肠黏膜损伤。总之,外周和结肠中性粒细胞中MMP-9的上调调节了TNBS诱导的结肠炎大鼠的透壁性结肠损伤。