Pivotal role of matrix metalloproteinase 13 in extracellular matrix turnover in idiopathic pulmonary fibrosis.

Takwi Nkyimbeng, Clemens Ruppert, Takayuki Shiomi, Bhola Dahal, György Lang, Werner Seeger, Yasunori Okada, Jeanine D'Armiento, Andreas Günther

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by excessive deposition of extracellular matrix (ECM). We investigated the regulation of matrix metalloproteinases (MMPs) and their inhibitors (TIMPs) in lung fibrosis. MMP and TIMP expression, collagenolytic activity and collagen content was assessed in IPF (n=16) versus donor (n=6) lung homogenates and accomplished by in-situ-zymography for gelatinolytic and collagenolytic activities, combined with MMP antigen detection. Role of MMP13 was assessed employing the bleomycin model of lung fibrosis in MMP-13(-/-) versus wild-type mice. In IPF, MMPs-1, 2, 7, 9 and 13, but not MMP-8, were significantly upregulated, whereas none of the TIMPs (1-4) were significantly altered. Collagen content was slightly increased and collagenolytic activity was most prominent in the airways and co-localized with MMP-13. We observed an exaggerated early inflammatory response and an augmented lung fibrosis in bleomycin-challenged MMP-13(-/-) versus wild-type mice, with elevated lung collagen content 28d after bleomycin challenge in the MMP-13(-/-) mice. Our data suggest that i) collagen deposition in IPF lungs is not primarily due to excessive TIMP production, but rather due to overwhelming ECM production in face of an overall increased, but spatially imbalanced collagenolytic activity, ii) preferential distribution of collagenolytic activity, largely MMP-13, in the airways offers an explanation for the development of honeycomb cysts and iii) despite an overall increase in inflammatory cell content the presence of MMP-13 seems to limit the overall extent of ECM deposition in lung fibrosis.

Original languageEnglish
Article numbere73279
JournalPLoS One
Volume8
Issue number9
Publication statusPublished - 2013

Fingerprint

Matrix Metalloproteinase 13
Idiopathic Pulmonary Fibrosis
fibrosis
extracellular matrix
Extracellular Matrix
lungs
Collagen
Lung
Fibrosis
Matrix Metalloproteinases
collagen
metalloproteinases
Matrix Metalloproteinase 8
Matrix Metalloproteinase 1
Tissue Inhibitor of Metalloproteinase-1
Matrix Metalloproteinase Inhibitors
Bleomycin
Matrix Metalloproteinase 2
neutrophil collagenase
mice

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Nkyimbeng, T., Ruppert, C., Shiomi, T., Dahal, B., Lang, G., Seeger, W., ... Günther, A. (2013). Pivotal role of matrix metalloproteinase 13 in extracellular matrix turnover in idiopathic pulmonary fibrosis. PLoS One, 8(9), [e73279].

Pivotal role of matrix metalloproteinase 13 in extracellular matrix turnover in idiopathic pulmonary fibrosis. / Nkyimbeng, Takwi; Ruppert, Clemens; Shiomi, Takayuki; Dahal, Bhola; Lang, György; Seeger, Werner; Okada, Yasunori; D'Armiento, Jeanine; Günther, Andreas.

In: PLoS One, Vol. 8, No. 9, e73279, 2013.

Research output: Contribution to journalArticle

Nkyimbeng, T, Ruppert, C, Shiomi, T, Dahal, B, Lang, G, Seeger, W, Okada, Y, D'Armiento, J & Günther, A 2013, 'Pivotal role of matrix metalloproteinase 13 in extracellular matrix turnover in idiopathic pulmonary fibrosis.', PLoS One, vol. 8, no. 9, e73279.
Nkyimbeng T, Ruppert C, Shiomi T, Dahal B, Lang G, Seeger W et al. Pivotal role of matrix metalloproteinase 13 in extracellular matrix turnover in idiopathic pulmonary fibrosis. PLoS One. 2013;8(9). e73279.
Nkyimbeng, Takwi ; Ruppert, Clemens ; Shiomi, Takayuki ; Dahal, Bhola ; Lang, György ; Seeger, Werner ; Okada, Yasunori ; D'Armiento, Jeanine ; Günther, Andreas. / Pivotal role of matrix metalloproteinase 13 in extracellular matrix turnover in idiopathic pulmonary fibrosis. In: PLoS One. 2013 ; Vol. 8, No. 9.
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