Background and Aims: In addition to its crucial role in dampening tissue-damaging immune responses in the gut, transforming growth factor beta (TGF beta) is a potent profibrogenic agent inducing collagen synthesis and regulating the balance between matrix-degrading matrix metalloproteinases (MMPs) and their inhibitors (TIMPs). TGF beta 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-TGF beta blocking antibody or TGF beta 1. TGF beta 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: TGF beta 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 TGF beta transcripts, a greater pSmad2-3 response to TGF beta, increased TIMP-1, lower Smad7, increased collagen production and reduced migration ability compared with myofibroblasts from mucosa overlying non-strictured gut. TGF beta 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.

Di Sabatino, A., Jackson, C., Pickard, K., Buckley, M., Rovedatti, L., Leakey, N., et al. (2009). Transforming growth factor beta signalling and matrix metalloproteinases in the mucosa overlying Crohn's disease strictures. GUT, 58(6), 777-789 [10.1136/gut.2008.149096].

Transforming growth factor beta signalling and matrix metalloproteinases in the mucosa overlying Crohn's disease strictures

MONTELEONE, GIOVANNI;
2009-01-01

Abstract

Background and Aims: In addition to its crucial role in dampening tissue-damaging immune responses in the gut, transforming growth factor beta (TGF beta) is a potent profibrogenic agent inducing collagen synthesis and regulating the balance between matrix-degrading matrix metalloproteinases (MMPs) and their inhibitors (TIMPs). TGF beta 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-TGF beta blocking antibody or TGF beta 1. TGF beta 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: TGF beta 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 TGF beta transcripts, a greater pSmad2-3 response to TGF beta, increased TIMP-1, lower Smad7, increased collagen production and reduced migration ability compared with myofibroblasts from mucosa overlying non-strictured gut. TGF beta 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.
2009
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/12 - GASTROENTEROLOGIA
English
Con Impact Factor ISI
macrophage elastase; Smad protein; Smad2 protein; Smad3 protein; Smad7 protein; steroid; stromelysin; tissue inhibitor of metalloproteinase 1; transforming growth factor beta; transforming growth factor beta antibody; transforming growth factor beta1; adult; apoptosis; article; cell migration; clinical article; controlled study; Crohn disease; enzyme activity; enzyme synthesis; human; human cell; human tissue; immunoblotting; in vitro study; mucosa; myofibroblast; priority journal; protein analysis; protein expression; protein phosphorylation; reverse transcription polymerase chain reaction; wound healing; Adult; Aged; Apoptosis; Blotting, Western; Case-Control Studies; Cell Aging; Cells, Cultured; Colon; Crohn Disease; Fibroblasts; Fibrosis; Humans; Intestinal Mucosa; Matrix Metalloproteinase 12; Matrix Metalloproteinase 3; Matrix Metalloproteinases; Middle Aged; Reverse Transcriptase Polymerase Chain Reaction; Signal Transduction; Smad2 Protein; Smad3 Protein; Tissue Inhibitor of Metalloproteinase-1; Transforming Growth Factor beta; Young Adult
Di Sabatino, A., Jackson, C., Pickard, K., Buckley, M., Rovedatti, L., Leakey, N., et al. (2009). Transforming growth factor beta signalling and matrix metalloproteinases in the mucosa overlying Crohn's disease strictures. GUT, 58(6), 777-789 [10.1136/gut.2008.149096].
Di Sabatino, A; Jackson, C; Pickard, K; Buckley, M; Rovedatti, L; Leakey, N; Picariello, L; Cazzola, P; Monteleone, G; Tonelli, F; Corazza, G; Macdonald, T; Pender, S
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/39146
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