Reversal of Myofibroblast Differentiation by Prostaglandin E2

G Garrison, SK Huang, K Okunishi, JP Scott… - American journal of …, 2013 - atsjournals.org
G Garrison, SK Huang, K Okunishi, JP Scott, LR Kumar Penke, AM Scruggs…
American journal of respiratory cell and molecular biology, 2013atsjournals.org
Differentiation of fibroblasts into α-smooth muscle actin (SMA)–expressing myofibroblasts
represents a critical step in the pathogenesis of fibrotic disorders, and is generally regarded
as irreversible. Prostaglandin E2 (PGE2) has been shown to prevent multiple aspects of
fibroblast activation, including the differentiation of fibroblasts to myofibroblasts. Here, we
investigated its ability to reverse this differentiated phenotype. Fetal and adult lung
fibroblasts were induced to differentiate into myofibroblasts by 24-hour culture with …
Differentiation of fibroblasts into α-smooth muscle actin (SMA)–expressing myofibroblasts represents a critical step in the pathogenesis of fibrotic disorders, and is generally regarded as irreversible. Prostaglandin E2 (PGE2) has been shown to prevent multiple aspects of fibroblast activation, including the differentiation of fibroblasts to myofibroblasts. Here, we investigated its ability to reverse this differentiated phenotype. Fetal and adult lung fibroblasts were induced to differentiate into myofibroblasts by 24-hour culture with transforming growth factor (TGF)-β1 or endothelin-1. Cells were then treated without or with PGE2 for various intervals and assessed for α-SMA expression. In the absence of PGE2 treatment, α-SMA expression induced by TGF-β1 was persistent and stable for up to 8 days. By contrast, PGE2 treatment effected a dose-dependent decrease in α-SMA and collagen I expression that was observed 2 days after PGE2 addition, peaked at 3 days, and persisted through 8 days in culture. This effect was not explained by an increase in myofibroblast apoptosis, and indeed, reintroduction of TGF-β1 2 days after addition of PGE2 prompted dedifferentiated fibroblasts to re-express α-SMA, indicating redifferentiation to myofibroblasts. This effect of PGE2 was associated with inhibition of focal adhesion kinase signaling, and a focal adhesion kinase inhibitor was also capable of reversing myofibroblast phenotype. These data unambiguously demonstrate reversal of established myofibroblast differentiation. Because many patients have established or even advanced fibrosis by the time they seek medical attention, this capacity of PGE2 has the potential to be harnessed for therapy of late-stage fibrotic disorders.
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