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Active synthesis of type I collagen homotrimer in Dupuytren’s fibrosis is unaffected by anti–TNF-α treatment
Kate Williamson, Katie J. Lee, Emma L. Beamish, Alan Carter, Jade A. Gumbs, Gabriella Cooper, Niamh S. O’Heneghan-Yates, Lisa A. Menezes, Graham Cheung, Daniel Brown, Rob Pettitt, Brendan Geraghty, Lucy A. Bosworth, Eithne J. Comerford, Peter D. Clegg, Elizabeth G. Canty-Laird
Kate Williamson, Katie J. Lee, Emma L. Beamish, Alan Carter, Jade A. Gumbs, Gabriella Cooper, Niamh S. O’Heneghan-Yates, Lisa A. Menezes, Graham Cheung, Daniel Brown, Rob Pettitt, Brendan Geraghty, Lucy A. Bosworth, Eithne J. Comerford, Peter D. Clegg, Elizabeth G. Canty-Laird
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Research Article Cell biology Therapeutics

Active synthesis of type I collagen homotrimer in Dupuytren’s fibrosis is unaffected by anti–TNF-α treatment

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Abstract

Dupuytren’s disease is a common fibroproliferative disease of the palmar fascia of the hand, with advanced cases treated surgically. Anti-TNF injection has undergone phase 2 trials and may be effective in slowing early-stage disease progression. Here we sought to determine how new synthesis of type I collagen in Dupuytren’s differs from normal palmar fascia samples and to analyze the role of TNF in aberrant collagen synthesis. Model nonfibrotic but fibrous connective tissues were used to analyze active type I collagen protein synthesis in development, aging, and degenerative disease, where it was restricted to early development and ruptured tissue. Dupuytren’s tissue was shown to actively synthesize type I collagen, including abnormal type I collagen homotrimer. TNF-α reduced COL1A2 gene expression only in the presence of serum in 2D cell culture and had opposing effects on collagen protein production in the presence or absence of serum. TNF-α had only limited effects in 3D tendon–like constructs. Anti-TNF did not reduce type I collagen synthesis in 3D tendon–like constructs or prevent type I collagen homotrimer synthesis in Dupuytren’s tissue. Hence, modulation of the TNF-α pathway in Dupuytren’s disease is unlikely to prevent the pathological collagen accumulation that is characteristic of fibrosis.

Authors

Kate Williamson, Katie J. Lee, Emma L. Beamish, Alan Carter, Jade A. Gumbs, Gabriella Cooper, Niamh S. O’Heneghan-Yates, Lisa A. Menezes, Graham Cheung, Daniel Brown, Rob Pettitt, Brendan Geraghty, Lucy A. Bosworth, Eithne J. Comerford, Peter D. Clegg, Elizabeth G. Canty-Laird

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Figure 4

Effect of TNF-α on type I collagen gene expression and collagen protein production in Dupuytren’s cells.

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Effect of TNF-α on type I collagen gene expression and collagen protein ...
(A–F) Analysis of COL1A1 (A and D), COL1A2 (B and D), and COL1A1/COL1A2 (C and F) gene expression by qPCR in normal PF, Dupuytren’s nodule, and Dupuytren’s cord cells (n = 4) after TNF-α treatment in serum-free conditions (–) (A–C) or in the presence of 10% FCS (+) (D–F). (G–I) Densitometric quantification of the relative amounts of radiolabeled collagen present in conditioned media from normal PF, Dupuytren’s nodule, and Dupuytren’s cord cells (n = 4) after TNF-α treatment, as compared with control treatments, in serum-free conditions (–) (G), the presence of 10% FCS (+) (H), or in both conditions (I). *P < 0.05, **P < 0.01, and ***P < 0.001 indicated between cell types, or between conditions in the key, by 2-way ANOVA with Holm-Šidák post-hoc test. Data shown in G and H were tested with 1-way ANOVA and 1-sample t-tests. Sample details are given in Supplemental Table 3. In E, the * indicates a significant difference between Control (+) and TNF-α (+). In I, the ** indicates a significant difference between TNF-α (–) and TNF-α (+). Please add suitable bracket in the key and move asterisks to indicate the differences.

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