Specific Differences in Migratory Function of Myofibroblasts Isolated from Crohn's Disease Fistulae and Strictures

被引:29
作者
Meier, Johannes K. -H. [2 ]
Scharl, Michael [1 ]
Miller, Sandra N. [3 ]
Brenmoehl, Julia [2 ]
Hausmann, Martin [1 ]
Kellermeier, Silvia [1 ]
Schoelmerich, Juergen [3 ]
Rogler, Gerhard [1 ]
机构
[1] Univ Zurich Hosp, Dept Internal Med, Div Gastroenterol & Hepatol, CH-8091 Zurich, Switzerland
[2] Univ Regensburg, Dept Craniomaxillofacial Surg, D-8400 Regensburg, Germany
[3] Univ Regensburg, Dept Internal Med 1, D-8400 Regensburg, Germany
关键词
Crohn's disease; fibrosis; myofibroblasts; migration; focal adhesion kinase; FOCAL ADHESION KINASE; INFLAMMATORY-BOWEL-DISEASE; CELL-MIGRATION; FIBROBLAST MIGRATION; FIBRONECTIN; INTERFERON; MECHANISMS; FAK; PATHOGENESIS; TGF-BETA-1;
D O I
10.1002/ibd.21344
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Recently we found that migration of colonic lamina propria fibroblasts in Crohn's disease patients (CD-CLPF) from inflamed mucosa is significantly reduced as compared to control-CLPF. The behavior of CD-CLPFs isolated from fistulae and strictures was now investigated in detail. Methods: Initially migration assays for all CLPF cultures (CD-CLPF, fibrosis-CLPF, and fistula-CLPF) were performed in the modified 48-well Boyden chamber. Subsequently, for a migration assay more resembling the in vivo situation a 3D matrix model was developed. After seeding of cells into the 3D matrix the CLPF layer was wounded by an ERBIUM:YAG laser leading to circular cell rupture without effect on the extracellular matrix. Results: In the modified Boyden chamber migration of fistula-CLPF was significantly reduced compared to CD-CLPF. This was correlated with a decrease in FAK-protein expression, whereas in migrating fibrosis-CLPF an increase in FAK-protein expression, -autophosphorylation and migratory potential was found. This was confirmed in the 3D matrix wounding assay: Fistula-CLPF migrated less than CD-CLPF, whereas fibrosis-CLPF migrated significantly more in the 3D matrix wounding assay. Between 1 to 36 hours incubation time fibrosis-CLPF always displayed increased migration ability as compared to CD-CLPF. In contrast, fistula-CLPF migratory potential was always below that of CD-CLPF. Conclusions: Myofibroblasts isolated from inflamed, fibrostenotic, or fistulized CD mucosa differ in their migratory potential both in the modified Boyden chamber as well as in a 3D matrix model. These different migratory behaviors could be an explanation for impaired or excess wound healing and subsequently for fistula and fibrosis formation.
引用
收藏
页码:202 / 212
页数:11
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