Beckett C G, Dell'Olio D, Ellis H J, Rosen-Bronson S, Ciclitira P J
Gastroenterology Unit, UMDS, St Thomas' Hospital, London, UK.
Eur J Gastroenterol Hepatol. 1998 Aug;10(8):641-7.
To investigate whether there are increased numbers of inducible nitric oxide synthase (iNOS) containing cells in the small intestine of patients with coeliac disease and the localization of nitric oxide synthase production.
Small intestinal biopsy specimens from patients with coeliac disease (11 untreated, 10 treated) and nine disease controls were studied.
Histochemical staining of sections for NADPH-diaphorase activity was performed, which gives an indication of NOS activity. iNOS protein was detected with immunohistochemistry and iNOS mRNA expression was detected using in situ hybridization with an oligonucleotide probe cocktail for iNOS. Cell phenotype was detected using monoclonal antibodies to CD3 (T-lymphocytes) and CD45 (total inflammatory cell infiltrate).
There was significantly greater NADPH diaphorase staining in the lamina propria of patients with untreated coeliac disease (P < 0.005). The same pattern was found for immunohistochemical and in situ hybridization methods of staining for iNOS in each of the patient groups (P < 0.005) but no epithelial staining was seen with any method. The pattern of iNOS staining in the lamina propria appeared in a similar distribution to that of the inflammatory cell infiltrate. At least 80% of the significantly increased total inflammatory cell infiltrate (CD45) in the lamina propria of patients with untreated coeliac disease was lymphocytic (CD3) whilst the iNOS staining cells made up less than 15% of the total inflammatory cell infiltrate.
There is a significant increase in the number of NOS staining cells of the inducible isoform in the lamina propria of patients with untreated coeliac disease. The lamina propria and not the epithelium is the site of iNOS production in coeliac disease. It appears that inflammatory cells other than T-lymphocytes are likely to be the cellular sources of iNOS production within the lamina propria. This is the first study to demonstrate increased numbers of iNOS producing cells in the small intestine of patients with untreated coeliac disease and suggests a role for nitric oxide in the pathogenesis of the histological changes seen in coeliac disease although it may be a non-specific inflammatory response to immune activation by gluten in susceptible individuals.
研究乳糜泻患者小肠中含诱导型一氧化氮合酶(iNOS)的细胞数量是否增加以及一氧化氮合酶产生的定位。
对乳糜泻患者(11例未治疗、10例已治疗)和9例疾病对照者的小肠活检标本进行研究。
对切片进行NADPH - 黄递酶活性的组织化学染色,以指示一氧化氮合酶活性。用免疫组织化学检测iNOS蛋白,并用针对iNOS的寡核苷酸探针混合物进行原位杂交检测iNOS mRNA表达。使用抗CD3(T淋巴细胞)和抗CD45(总炎性细胞浸润)的单克隆抗体检测细胞表型。
未治疗的乳糜泻患者固有层中NADPH黄递酶染色明显更强(P < 0.005)。在每个患者组中,iNOS染色的免疫组织化学和原位杂交方法呈现相同模式(P < 0.005),但任何方法均未见到上皮染色。固有层中iNOS染色模式的分布与炎性细胞浸润相似。未治疗的乳糜泻患者固有层中显著增加的总炎性细胞浸润(CD45)中至少80%为淋巴细胞(CD3),而iNOS染色细胞占总炎性细胞浸润的比例不到15%。
未治疗的乳糜泻患者固有层中诱导型同工型一氧化氮合酶染色细胞数量显著增加。乳糜泻中iNOS产生的部位是固有层而非上皮。看来除T淋巴细胞外的炎性细胞可能是固有层中iNOS产生的细胞来源。这是第一项证明未治疗的乳糜泻患者小肠中产生iNOS的细胞数量增加的研究,并提示一氧化氮在乳糜泻所见组织学改变的发病机制中起作用,尽管它可能是对易感个体中麸质免疫激活的非特异性炎症反应。