Transforming growth factor β signalling and matrix metalloproteinases in the mucosa overlying Crohn’s disease strictures

肌成纤维细胞 基质金属蛋白酶 SMAD公司 转化生长因子 肠粘膜 生物 转化生长因子β 分子生物学 免疫学 化学 细胞生物学 病理 内科学 医学 纤维化 生物化学
作者
Antonio Di Sabatino,Claire Jackson,K. Pickard,Mark G. Buckley,L. Rovedatti,N. Leakey,Lucia Picariello,P. Cazzola,Giovanni Monteleone,Francesco Tonelli,Gino Roberto Corazza,Thomas T. MacDonald,Sylvia L. F. Pender
出处
期刊:Gut [BMJ]
卷期号:58 (6): 777-789 被引量:204
标识
DOI:10.1136/gut.2008.149096
摘要

BACKGROUND AND AIMS: In addition to its crucial role in dampening tissue-damaging immune responses in the gut, transforming growth factor beta (TGFbeta) is a potent profibrogenic agent inducing collagen synthesis and regulating the balance between matrix-degrading matrix metalloproteinases (MMPs) and their inhibitors (TIMPs). TGFbeta signalling was investigated by analysis of Smad proteins and MMPs/TIMPs in the mucosa overlying strictures in patients with Crohn's disease (CD). METHODS: Specimens were collected from macroscopically normal mucosa overlying strictured and non-strictured gut of patients with fibrostenosing CD. Isolated myofibroblasts were cultured with anti-TGFbeta blocking antibody or TGF beta 1. TGFbeta transcripts were analysed by quantitative reverse transcription-PCR (RT-PCR). Smad proteins and MMPs were determined by immunoblotting. MMP-12 activity was measured by a real-time MMP-12 activity assay. An in vitro wound-healing scratch assay was used to assess myofibroblast migration. RESULTS: TGFbeta transcripts, phosphorylated Smad2-Smad3 (pSmad2-3) and TIMP-1 proteins were higher in mucosa overlying strictures than in mucosa overlying non-strictured areas. In contrast, mucosa overlying strictured gut had lower expression of Smad7, MMP-12 and MMP-3. Myofibroblasts from mucosa overlying strictured gut showed higher TGFbeta transcripts, a greater pSmad2-3 response to TGFbeta, increased TIMP-1, lower Smad7, increased collagen production and reduced migration ability compared with myofibroblasts from mucosa overlying non-strictured gut. TGFbeta blockade increased myofibroblast MMP-12 production and migration, more obviously in myofibroblasts isolated from mucosa overlying non-strictured compared with strictured gut. CONCLUSIONS: Changes in TGF-beta signalling and MMP production were identified in the mucosa overlying strictures in CD which may give a window into the process of fibrosis.
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