Publication: Butylated hydroxytoluene induces type-V collagen and overexpression of remodeling genes/proteins in experimental lung fibrosis
Authors
Martins, Vanessa ; Teodoro, Walcy Rosolia ; Pereira Velosa, Ana Paula ; Andrade, Priscila ; Farhat, Cecília ; Fabro, Alexandre Todorovic ; Capelozzi, Vera Luiza
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Publisher
Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
DOI: 10.14670/HH-18-010
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info:eu-repo/semantics/article
Description
Abstract
Anomalous histoarchitecture with increased
levels of type-V collagen (Col V) in lungs of human
idiopathic pulmonary fibrosis (IPF) and bleomycin
(BLM) airway-centered interstitial fibrosis suggest that
this collagen can be a possible trigger involved in the
pathogenesis of these diseases. Butylated hydroxytoluene (BHT) injury model revealed a distal
involvement of lung parenchyma with significant
endothelial injury and fibrotic response, contrasting with
the BLM airway-centered insult. We undertook this
study to analyze whether BHT alters distal
airway/alveolar epithelial cells (AECs) and extracellular
matrix (ECM) signaling involved in the initiation and
progression of pulmonary fibrosis in a different pathway
concerning overexpression of Col V. Female mice
C57BL/6 (n=6) were instilled intraperitoneally with
400mg/kg of BHT dissolved in 1 mL of corn oil and
euthanized at day 14 or 21 after BHT administration.
Morphometry, immunohistochemistry and transmission
electron microscopy were performed to characterize
microscopic and submicroscopic changes of AECs and
endothelial cells through transforming growth factor beta
(TGF-β) basic fibroblast growth factor (bFGF) and
vascular endothelial growth factor (VEGF) expression.
Immunofluorescence and immunogold electron
microscopy were performed to characterize Col V.
Quantitative polymerase chain reaction (qPCR) was used
to confirm differential levels of RNA messenger. BHT
lungs showed marked fibrotic areas and hyperplastic
AECs. The alveolar damage caused destruction of elastic
fibers and a critical increase of Col V in ECM of distal
lung parenchyma. Fibrogenesis-promoting markers
TGF-β, bFGF and VEGF were also overexpressed in
situ, coinciding with up-regulation in remodeling
enzymes, growth factors, cytokines, transduction and
transcription genes. BHT alters distal lung parenchyma
signaling involved in pulmonary fibrosis highlighted
similarities to human IPF in a pathway involving Col V
arising as a promissory model to identify effective
therapeutic targets.
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Citation
Histology and Histopathology, Vol.33, nº10, (2018)
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