Pascual G, Corrales C, Gómez-Gil V, Buján J, Bellón J M
Faculty of Medicine, University of Alcala, Alcalá de Henares, Madrid, Spain.
Eur J Clin Invest. 2007 Jun;37(6):516-21. doi: 10.1111/j.1365-2362.2007.01816.x.
The aetiology of inguinal hernia includes changes in collagen turnover and metalloproteinase (MMP) expression, and direct hernia has been linked to increased MMP-2 expression. Since transforming growth factor beta1 (TGFbeta1) plays a role in tissue remodelling, this growth factor could directly affect metalloproteinase secretion and thus the proteolytic activity of these enzymes. We hypothesized that TGFbeta1 expression could also be altered in direct inguinal hernias.
Tissue specimens were obtained from the transversalis fascia (TF) of organ donors (controls; n = 10) and patients with inguinal hernia (indirect; n = 20/direct; n = 20), who were also divided into two groups according to age (20-40/41-60 years). Tissue sections were immunohistochemically labelled using anti-LAP TGFbeta1 (latent form) and anti-TGFbeta1 (active form) antibodies, and fragments of tissue were subjected to Western blot analysis.
No significant differences in LAP-TGFbeta1 expression were detected between specimens from control and hernia patients. However, significantly higher levels of active TGFbeta1 were detected in the TF of patients with direct hernia (P < 0.05). Age affected the expression of the growth factor in its active form, and significant differences emerged between direct hernias and controls/indirect hernias only in the younger age groups.
Our findings indicate overexpression of the active form of TGFbeta1 in the TF of young patients with direct hernia. This overexpression reflects an attempt to counterbalance the enhanced matrix degradation process observed in these patients, identifying a subset of patients requiring the use of a prosthetic material for primary hernia repair.
腹股沟疝的病因包括胶原蛋白更新和金属蛋白酶(MMP)表达的变化,且直疝与MMP-2表达增加有关。由于转化生长因子β1(TGFβ1)在组织重塑中发挥作用,这种生长因子可能直接影响金属蛋白酶的分泌,进而影响这些酶的蛋白水解活性。我们推测TGFβ1表达在直疝中也可能发生改变。
从器官捐献者(对照组;n = 10)以及腹股沟疝患者(斜疝;n = 20/直疝;n = 20)的腹横筋膜(TF)获取组织标本,患者还根据年龄分为两组(20 - 40/41 - 60岁)。组织切片使用抗LAP TGFβ1(潜伏形式)和抗TGFβ1(活性形式)抗体进行免疫组织化学标记,组织碎片进行蛋白质印迹分析。
对照组和疝患者的标本中未检测到LAP - TGFβ1表达的显著差异。然而,在直疝患者的TF中检测到活性TGFβ1水平显著更高(P < 0.05)。年龄影响活性形式生长因子的表达,仅在较年轻年龄组中,直疝与对照组/斜疝之间出现显著差异。
我们的研究结果表明,年轻直疝患者的TF中TGFβ1活性形式过表达。这种过表达反映了试图平衡这些患者中观察到的增强的基质降解过程,确定了一部分需要使用人工材料进行原发性疝修补的患者亚组。