Abstract
Transforming growth factor-β (TGF-β) signaling plays an important and complex role in renal fibrogenesis. The seemingly simple TGF-β/Smad cascade is intensively regulated at several levels, including crosstalk with other signaling pathways. Epidermal growth factor (EGF) is a potent mitogen for epithelial cells and is elevated in diseased kidneys. In this study, we examined its effect on TGF-β-induced fibrotic changes in human proximal tubular epithelial cells. Simultaneous treatment with EGF specifically inhibited basal and TGF-β-induced type-I collagen and α-smooth muscle actin (αSMA) expression at both mRNA and protein levels. These effects were prevented by inhibition of either the EGF receptor kinase or its downstream MEK kinase but not by blockade of either the JNK or PI3K pathway. Overexpression of a constitutively active MEK1 construct mimicked the inhibitory effect of EGF. Further, EGF suppressed Smad transcriptional activities, as shown by reduced activation of ARE-luc and SBE-luc. Both reductions were prevented by MEK inhibition. However, EGF did not block Smad2 or Smad3 phosphorylation by TGF-β, or Smad2/3 nuclear import. Finally EGF induced the phosphorylation and expression of TGIF, a known TGF-β/Smad repressor. Both the phosphorylation and the induction were blocked by a MEK inhibitor. Overexpression of TGIF abolished TGF-β-induced αSMA promoter activity. Together these results suggest that EGF inhibits two TGF-β-stimulated markers of EMT through EGF receptor tyrosine kinase and downstream ERK activation, but not through PI3K or JNK. The inhibition results from effector mechanisms downstream of Smads, and most likely involves the transcriptional repressor, TGIF.
Original language | English (US) |
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Pages (from-to) | 2276-2283 |
Number of pages | 8 |
Journal | Cellular Signalling |
Volume | 26 |
Issue number | 10 |
DOIs | |
State | Published - Oct 2014 |
Funding
We thank Dr. R. Schwartz, Dr. B. Vogelstein and Dr. D. Wotton for providing us with the plasmids, and Dr. L. Racusen for sharing the human proximal tubular epithelial cell line. We also appreciate the discussions and inputs from Dr. T. Hayashida (Northwestern University, Chicago, IL). This work was supported by the grant RO1 DK049362 from the National Institute of Diabetes, Digestive and Kidney Diseases to H.W.S.
Keywords
- EGF
- EMT
- ERK
- Fibrosis
- Smad2/3
- TGF-β
ASJC Scopus subject areas
- Cell Biology