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Cited by 529

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Role of Epithelial Cells in Idiopathic Pulmonary Fibrosis: From Innocent Targets to Serial Killers

Selman, Moisés, Pardo, Annie·2006·Proceedings of the American Thoracic Society

Abstract

Idiopathic pulmonary fibrosis (IPF), a progressive and relentless lung scarring of unknown etiology, has been recognized as the most lethal interstitial lung disease. Despite the growing interest in IPF, the precise molecular mechanisms underlying the development of fibrosis and leading to the irreversible destruction of the lung are still unknown. Recently, it has been proposed that IPF, instead of being a chronic inflammatory disorder, results from multiple cycles of epithelial cell injury and activation. In turn, active alveolar epithelial cells provoke the migration, proliferation, and activation of mesenchymal cells with the formation of fibroblastic/myofibroblastic foci and the exaggerated accumulation of extracellular matrix, mirroring abnormal wound repair. In this article, some characteristics of the alveolar epithelium are briefly outlined, and the fibrogenic mechanisms specifically operated by active abnormal epithelial cells are examined.

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Crossref · 10.1513/pats.200601-003tk

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Metadata

Authors
Selman, M., & Pardo, A.
Venue
Proceedings of the American Thoracic Society
Published
2006-06-01
Volume
3
Issue
4
Pages
364-372
ISSN
  • 1546-3222 (ISSN-L)
  • 1943-5665
OpenAlex
W2104778949
Cited by
529
References
2
FWCI
17.17
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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