Fitzpatrick Leo R, Small Jeffrey S, Poritz Lisa S, McKenna Kevin J, Koltun Walter A
Department of Surgery, Section of Colon and Rectal Surgery, Penn State College of Medicine, Hershey, Pennsylvania 17033, USA.
Dis Colon Rectum. 2007 Mar;50(3):337-48; discussion 348-50. doi: 10.1007/s10350-006-0796-7.
Low molecular mass polypeptide 2 is an inducible immunoproteasome subunit. The expression of low molecular mass polypeptide 2 has not been examined in the intestine of patients with inflammatory bowel disease. This study was designed to determine whether the intestinal expression of low molecular mass polypeptide 2 was enhanced in a group of patients with inflammatory bowel disease compared with a group of control patients without inflammatory bowel disease. Moreover, we examined the association between low molecular mass polypeptide 2 expression and histologic pathology in these patients.
Twenty-one patients participated in the study. These included six control subjects without inflammatory bowel disease, eight patients with ulcerative colitis, and seven patients with Crohn's disease. Intestinal low molecular mass polypeptide 2 expression was evaluated by immunohistochemistry, as well as by Western blot. Histology scores (0-40 severity scale) were determined on the same sections of intestine as those used for low molecular mass polypeptide 2 histochemistry.
By immunohistochemistry, low molecular mass polypeptide 2 expression was significantly enhanced (P < 0.05 vs. control subjects) throughout visibly diseased areas of colon, rectum, and ileum from patients with inflammatory bowel disease. Low molecular mass polypeptide 2 expression also was increased in macroscopically normal intestine from patients with inflammatory bowel disease compared with normal tissue from control subjects. There was a significant correlation (P < 0.0001) between low molecular mass polypeptide 2 expression and histologic pathology in our patients. Western blot results confirmed that low molecular mass polypeptide 2 expression was enhanced in patients with ulcerative colitis (3.1-fold) and in patients with Crohn's disease (3.5-fold).
Intestinal low molecular mass polypeptide 2 expression is significantly increased in inflammatory bowel disease. The association between intestinal low molecular mass polypeptide 2 expression and histologic pathology suggests that this proteasome subunit plays a role in the pathogenesis of inflammatory bowel disease.
低分子量多肽2是一种可诱导的免疫蛋白酶体亚基。尚未在炎症性肠病患者的肠道中检测过低分子量多肽2的表达。本研究旨在确定与一组无炎症性肠病的对照患者相比,一组炎症性肠病患者的肠道中低分子量多肽2的表达是否增强。此外,我们研究了这些患者中低分子量多肽2表达与组织病理学之间的关联。
21名患者参与了本研究。其中包括6名无炎症性肠病的对照受试者、8名溃疡性结肠炎患者和7名克罗恩病患者。通过免疫组织化学以及蛋白质印迹法评估肠道低分子量多肽2的表达。组织学评分(0 - 40严重程度量表)在与用于低分子量多肽2组织化学的相同肠道切片上确定。
通过免疫组织化学,炎症性肠病患者结肠、直肠和回肠明显病变区域的低分子量多肽2表达显著增强(与对照受试者相比,P < 0.05)。与对照受试者的正常组织相比,炎症性肠病患者宏观上正常的肠道中低分子量多肽2表达也增加。在我们的患者中,低分子量多肽2表达与组织病理学之间存在显著相关性(P < 0.0001)。蛋白质印迹结果证实,溃疡性结肠炎患者(3.1倍)和克罗恩病患者(3.5倍)的低分子量多肽2表达增强。
炎症性肠病中肠道低分子量多肽2表达显著增加。肠道低分子量多肽2表达与组织病理学之间的关联表明,这种蛋白酶体亚基在炎症性肠病的发病机制中起作用。