Bouatrouss Y, Herring-Gillam F E, Gosselin J, Poisson J, Beaulieu J F
Département d'anatomie et de biologie cellulaire, Medical Research Council Group in Functional Development and Physiopathology of the Digestive Tract, Faculté de médecine, Université de Sherbrooke, Canada.
Am J Pathol. 2000 Jan;156(1):45-50. doi: 10.1016/S0002-9440(10)64704-9.
Laminins are a large family of heterotrimeric basement membrane molecules that mediate crucial cell functions such as adhesion, proliferation, migration, and differentiation. Up to now, three distinct laminins have been identified in the normal human small intestinal epithelium. Laminin-1 (alpha1beta1gamma1) and laminin-5 (alpha3beta3gamma2) are mainly expressed at the base of villus cells, whereas laminin-2 (alpha2beta1gamma1) is restricted to the bottom of the crypts. The expression of these molecules has not yet been studied in Crohn's disease (CD), but it could be altered, in light of the important changes occurring in the architecture of the crypt-villus axis under the active state of the disease. To test this hypothesis, the expression of laminin alpha1, alpha2, and alpha3 subunits was analyzed in control, inflamed, and corresponding uninflamed CD small intestinal specimens by indirect immunofluorescence and reverse transcriptase-polymerase chain reaction. Surprisingly, alpha1 and alpha3 remained strongly expressed by all villus cells, whereas alpha2, normally expressed in the bottom of the crypts in control and uninflamed CD specimens, was lacking in inflamed CD specimens. However, this loss of alpha2 expression was associated with a significant up-regulation of both alpha1 and alpha3 expression in the crypts of inflamed CD specimens. A significant up-regulation of the alpha1 subunit was also observed in the crypts of uninflamed CD specimens. At the transcript levels, alpha1 was found significantly higher in inflamed than uninflamed CD specimens. Taken together, these observations identify important alterations in laminin expression in the small intestine with CD and suggest that compositional changes in the epithelial basement membrane may play a role in this disease.
层粘连蛋白是一个由异源三聚体组成的大型基底膜分子家族,介导细胞的关键功能,如黏附、增殖、迁移和分化。到目前为止,已在正常人类小肠上皮中鉴定出三种不同的层粘连蛋白。层粘连蛋白-1(α1β1γ1)和层粘连蛋白-5(α3β3γ2)主要表达于绒毛细胞底部,而层粘连蛋白-2(α2β1γ1)局限于隐窝底部。这些分子在克罗恩病(CD)中的表达尚未被研究,但鉴于疾病活动状态下隐窝-绒毛轴结构发生的重要变化,其表达可能会改变。为了验证这一假设,通过间接免疫荧光和逆转录聚合酶链反应,分析了对照、炎症和相应非炎症CD小肠标本中层粘连蛋白α1、α2和α3亚基的表达。令人惊讶的是,所有绒毛细胞均强烈表达α1和α3,而在对照和非炎症CD标本中正常表达于隐窝底部的α2,在炎症CD标本中缺失。然而,α2表达的缺失与炎症CD标本隐窝中α1和α3表达的显著上调相关。在非炎症CD标本的隐窝中也观察到α1亚基的显著上调。在转录水平上,发现炎症CD标本中的α1明显高于非炎症CD标本。综上所述,这些观察结果确定了CD患者小肠中层粘连蛋白表达的重要改变,并表明上皮基底膜的成分变化可能在该疾病中起作用。