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2018 ; 24
(ä): 1633-1641
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English Wikipedia
Specific Inhibitor of Smad3 (SIS3) Attenuates Fibrosis, Apoptosis, and
Inflammation in Unilateral Ureteral Obstruction Kidneys by Inhibition of
Transforming Growth Factor ? (TGF-?)/Smad3 Signaling
#MMPMID29555895
Ji X
; Wang H
; Wu Z
; Zhong X
; Zhu M
; Zhang Y
; Tan R
; Liu Y
; Li J
; Wang L
Med Sci Monit
2018[Mar]; 24
(ä): 1633-1641
PMID29555895
show ga
BACKGROUND Fibrosis is the common pathological feature in most kinds of chronic
kidney disease (CKD). TGF-?/Smads signaling is the master pathway regulating
kidney fibrosis pathogenesis, in which Smad3 acts as the integrator of various
pro-fibrosis signals. In this study, we analyzed the role of SIS3, a specific
inhibitor of Smad3, in mouse unilateral ureteral obstruction (UUO) kidneys.
MATERIAL AND METHODS UUO mice were intraperitoneally injected with 0.2 mg/kg/day
or 2 mg/kg/day of SIS3 or control saline for 7 days, followed by analysis of
structure injury, fibrosis status, inflammation, apoptosis, and TGF-?/Smads
signaling activity. RESULTS Our results indicated that SIS3 treatment
dosage-dependently relieved the gross structure injury and tubular necrosis in
UUO kidneys. Masson staining, immunohistochemistry, and real-time PCR showed
significantly decreased extracellular matrix deposition, fibronectin staining
intensity, and RNA levels of collagen I and collagen III in SIS3-treated UUO
kidneys. SIS3 treatment also suppressed the activation of myofibroblasts, as
evidenced by decreased expression levels of a-SMA and vimentin in UUO kidneys.
The TGF-?/Smads signaling activity analysis showed that SIS3 inhibited the
phosphorylation of Smad3 but not Smad2 and decreased the protein level of TGF-?1,
suggesting specific inhibition of the TGF-?/Smad3 pathway in UUO kidneys.
Furthermore, SIS3 treatment also ameliorated the increased pro-inflammatory TNF-?
and COX2 in UUO kidneys and circulating IL-1? in UUO mice, and inhibited
caspase-3 activity and the number of apoptotic cells. CONCLUSIONS SIS3
ameliorated fibrosis, apoptosis, and inflammation through inhibition of
TGF-b/Smad3 signaling in UUO mouse kidneys.