Department of Pharmaceutical Technology and Biopharmacy, Groningen Research Institute of Pharmacy, University of Groningen, 9713 AV Groningen, The Netherlands.
Biomarkers and Research, Nordic Bioscience, 2730 Herlev, Denmark.
Cells. 2024 Jun 22;13(13):1084. doi: 10.3390/cells13131084.
In Crohn's Disease (CD), intestinal fibrosis is a prevalent yet unresolved complication arising from chronic and transmural inflammation. The histological assessment of CD intestines shows changes in tissue morphology in all the layers, including the mucosa and muscularis. This study aimed to determine the differences in fibrogenesis between mucosa and muscularis. Human precision-cut intestinal slices (hPCIS) were prepared from human intestine mucosa and muscularis and treated with TGF-β1 and/or PDGF-BB for 72 h. Gene and protein expression and matrix metalloproteinase (MMP) activity were determined. The basal gene expression of various fibrosis markers was higher in muscularis compared to mucosa hPCIS. During incubation, Pro-Collagen-1A1 secretion increased in muscularis but not in mucosa hPCIS. MMP gene expression increased during incubation in mucosa and muscularis hPCIS, except for MMP9, MMP12, and MMP13 in muscularis hPCIS. Incubation with TGF-β1 caused increased COL1A1 expression in the mucosa but not in muscularis hPCIS. In muscularis hPCIS, TGF-β1 treatment caused a decrease in MMP1 and CTSK expression, while MMP13 was increased. In the presence of TGF-β1, protease inhibitor expression was stable, except for SERPINE1, which was increased in muscularis hPCIS. We conclude that fibrogenesis is more pronounced in muscularis hPCIS compared to mucosa hPCIS, especially when stimulated with TGF-β1.
在克罗恩病(CD)中,肠纤维化是一种普遍存在但尚未解决的并发症,它源于慢性和贯穿性炎症。对 CD 肠道的组织学评估显示,所有层的组织形态都发生了变化,包括黏膜和肌层。本研究旨在确定黏膜和肌层之间纤维化发生的差异。从人肠黏膜和肌层制备人精确切割肠切片(hPCIS),并用 TGF-β1 和/或 PDGF-BB 处理 72 小时。测定基因和蛋白质表达及基质金属蛋白酶(MMP)活性。与黏膜 hPCIS 相比,各种纤维化标志物的基础基因表达在肌层中更高。孵育期间,肌层中 Pro-Collagen-1A1 的分泌增加,但黏膜 hPCIS 中没有增加。孵育期间,黏膜和肌层 hPCIS 中的 MMP 基因表达增加,但肌层 hPCIS 中的 MMP9、MMP12 和 MMP13 除外。TGF-β1 孵育导致黏膜 hPCIS 中 COL1A1 表达增加,但肌层 hPCIS 中没有增加。在肌层 hPCIS 中,TGF-β1 处理导致 MMP1 和 CTSK 表达减少,而 MMP13 增加。在存在 TGF-β1 的情况下,蛋白酶抑制剂表达稳定,除了肌层 hPCIS 中 SERPINE1 增加外。我们得出结论,与黏膜 hPCIS 相比,肌层 hPCIS 的纤维化更为明显,尤其是在受到 TGF-β1 刺激时。