Department of Physiology, Kwandong University College of Medicine, Gangneung 210-701, Korea.
Korean J Physiol Pharmacol. 2012 Jun;16(3):193-8. doi: 10.4196/kjpp.2012.16.3.193. Epub 2012 Jun 26.
Changes in the expression profiles of specific proteins leads to serious human diseases, including colitis. The proteomic changes related to colitis and the differential expression between tuberculous (TC) and ulcerative colitis (UC) in colon tissue from colitis patients has not been defined. We therefore performed a proteomic analysis of human TC and UC mucosal tissue. Total protein was obtained from the colon mucosal tissue of normal, TC, and UC patients, and resolved by 2-dimensional electrophoresis (2-DE). The results were analyzed with PDQuest using silver staining. We used matrix-assisted laser desorption ionization time-of-flight/time-of-flight spectrometry (MALDI TOF/TOF) to identify proteins differentially expressed in TC and UC. Of the over 1,000 proteins isolated, three in TC tissue and two in UC tissue displayed altered expression when compared to normal tissue. Moreover, two proteins were differentially expressed in a comparative analysis between TC and UC. These were identified as mutant β-actin, α-enolase and Charcot-Leyden crystal protein. In particular, the expression of α-enolase was significantly greater in TC compared with normal tissue, but decreased in comparison to UC, implying that α-enolase may represent a biomarker for differential diagnosis of TC and UC. This study therefore provides a valuable resource for the molecular and diagnostic analysis of human colitis.
特定蛋白质表达谱的变化会导致严重的人类疾病,包括结肠炎。结肠炎相关的蛋白质组变化以及结核性结肠炎(TC)和溃疡性结肠炎(UC)患者结肠组织之间的差异表达尚未确定。因此,我们对人类 TC 和 UC 黏膜组织进行了蛋白质组分析。从正常、TC 和 UC 患者的结肠黏膜组织中获得总蛋白,并通过二维电泳(2-DE)进行分离。使用银染法,用 PDQuest 分析结果。我们使用基质辅助激光解吸电离飞行时间/飞行时间质谱(MALDI TOF/TOF)鉴定 TC 和 UC 中差异表达的蛋白质。在分离的 1000 多种蛋白质中,有三种在 TC 组织中,两种在 UC 组织中与正常组织相比表达发生改变。此外,在 TC 和 UC 之间的比较分析中,有两种蛋白质表达差异。它们被鉴定为突变β-肌动蛋白、α-烯醇酶和 Charchot-Leyden 晶体蛋白。特别是,与正常组织相比,TC 中α-烯醇酶的表达显著增加,但与 UC 相比则减少,这意味着α-烯醇酶可能是 TC 和 UC 鉴别诊断的生物标志物。因此,本研究为人类结肠炎的分子和诊断分析提供了有价值的资源。