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Disruption of Smad4 impairs TGF-β/Smad3 and Smad7 transcriptional regulation during renal inflammation and fibrosis in vivo and in vitro.
- Source :
-
Kidney international [Kidney Int] 2012 Feb; Vol. 81 (3), pp. 266-79. Date of Electronic Publication: 2011 Nov 02. - Publication Year :
- 2012
-
Abstract
- The mechanism by which TGF-β regulates renal inflammation and fibrosis is largely unclear; however, it is well accepted that its biological effects are mediated through Smad2 and Smad3 phosphorylation. Following activation, these Smads form heteromeric complex with Smad4 and translocate into the nucleus to bind and regulate the expression of target genes. Here we studied the roles of Smad4 to regulate TGF-β signaling in a mouse model of unilateral ureteral obstruction using conditional Smad4 knockout mice and in isolated Smad4 mutant macrophages and fibroblasts. Disruption of Smad4 significantly enhanced renal inflammation as evidenced by a greater CD45(+) leukocyte and F4/80(+) macrophage infiltration and upregulation of IL-1β, TNF-α, MCP-1, and ICAM-1 in the obstructed kidney and in IL-1β-stimulated macrophages. In contrast, deletion of Smad4 inhibited renal fibrosis and TGF-β1-induced collagen I expression by fibroblasts. Further studies showed that the loss of Smad4 repressed Smad7 transcription, leading to a loss of functional protein. This, in turn, inhibited IκBα expression but enhanced NF-κB activation, thereby promoting renal inflammation. Interestingly, deletion of Smad4 influenced Smad3-mediated promoter activities and the binding of Smad3 to the COL1A2 promoter, but not Smad3 phosphorylation and nuclear translocation, thereby inhibiting the fibrotic response. Thus, Smad4 may be a key regulator for the diverse roles of TGF-β1 in inflammation and fibrogenesis by interacting with Smad7 and Smad3 to influence their transcriptional activities in renal inflammation and fibrosis.
- Subjects :
- Animals
Extracellular Signal-Regulated MAP Kinases physiology
Fibrosis
Gene Expression Regulation
Interleukin-1beta pharmacology
Mice
Mice, Inbred C57BL
NF-kappa B metabolism
Transcription, Genetic
Kidney pathology
Nephritis metabolism
Smad3 Protein physiology
Smad4 Protein physiology
Smad7 Protein physiology
Transforming Growth Factor beta physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1523-1755
- Volume :
- 81
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Kidney international
- Publication Type :
- Academic Journal
- Accession number :
- 22048127
- Full Text :
- https://doi.org/10.1038/ki.2011.327