Inhibition of ILK by QLT-0267 reduces β-catenin accumulation and inhibits Snail1 expression in obstructive nephropathy. Inhibition of ILK by QLT-0267 reduces.

Slides:



Advertisements
Similar presentations
by Koji Yamamoto, Vivian de Waard, Colleen Fearns, and David J
Advertisements

Volume 78, Issue 3, Pages (August 2010)
Canonical Wnt/β-catenin signaling mediates transforming growth factor-β1-driven podocyte injury and proteinuria  Dan Wang, Chunsun Dai, Yingjian Li, Youhua.
Pioglitazone treatment prevents TRPC6 overexpression and podocyte injury in the adriamycin (ADRIA)–induced nephropathy rat model for FSGS. ADRIA-induced.
Hui Ying Li, Yoon Sin Oh, Ji-Woong Choi, Ji Yong Jung, Hee-Sook Jun 
PDE5A is expressed by podocytes.
Volume 84, Issue 1, Pages (July 2013)
Inhibition of ILK by QLT-0267 suppresses type I and type III collagen expression and ameliorates interstitial collagen deposition and renal fibrosis after.
Sildenafil does not prevent TRPC6 overexpression and podocyte injury in adriamycin (ADRIA)–challenged podocyte-specific PPAR-γ KO mice. Sildenafil does.
TGF-β1 induces ILK activity in renal tubular epithelial cells.
Inhibition of ILK restores epithelial ZO-1 and E-cadherin and inhibits fibronectin and Snail1 expression after TGF-β1 treatment. Inhibition of ILK restores.
Volume 68, Issue 6, Pages (December 2005)
Podocyte-specific PPAR-γ–deficient mice show increased glomerular TRPC6 expression. Podocyte-specific PPAR-γ–deficient mice show increased glomerular TRPC6.
Inhibition of ILK activity does not affect normal kidney structure and nephrin/ILK interaction in vivo. Inhibition of ILK activity does not affect normal.
Inhibition of ILK by QLT-0267 abrogates PAI-1 and MMP-2 induction by TGF-β1 in tubular epithelial cells. Inhibition of ILK by QLT-0267 abrogates PAI-1.
Reduced cell motility and expression of phosphorylated FAK in a fibroblast cell line of an individual with T3257I mutation. Reduced cell motility and expression.
Tubular cell dedifferentiation and peritubular inflammation are coupled by the transcription regulator Id1 in renal fibrogenesis  Yingjian Li, Xiaoyan.
Small-molecule inhibitor QLT-0267 suppresses ILK activity and inhibits its downstream signaling. Small-molecule inhibitor QLT-0267 suppresses ILK activity.
Volume 78, Issue 4, Pages (August 2010)
Volume 70, Issue 4, Pages (August 2006)
Dong Zhou, Yingjian Li, Lin Lin, Lili Zhou, Peter Igarashi, Youhua Liu 
Ganesan Ramesh, W. Brian Reeves  Kidney International 
INT-767 treatment prevents the increase in renal inflammation and oxidative stress in diabetic DBA/2J mice. INT-767 treatment prevents the increase in.
IN-1130, a novel transforming growth factor-β type I receptor kinase (ALK5) inhibitor, suppresses renal fibrosis in obstructive nephropathy  J.-A. Moon,
INT-767 treatment prevents the increase in renal HIF and Glut1 expression and ER stress in diabetic DBA/2J mice. INT-767 treatment prevents the increase.
INT-767 treatment prevents renal lipid accumulation in diabetic DBA/2J mice. INT-767 treatment prevents renal lipid accumulation in diabetic DBA/2J mice.
Volume 86, Issue 3, Pages (September 2014)
Volume 88, Issue 3, Pages (September 2015)
Renal microvascular injury 6 months after induction of JG cell-specific Gsα knockout. Renal microvascular injury 6 months after induction of JG cell-specific.
Volume 75, Issue 2, Pages (January 2009)
Kameswaran Surendran, Theodore C. Simon, Helen Liapis, John K. McGuire 
Volume 56, Issue 6, Pages (December 1999)
Activation of hepatocyte growth factor receptor, c-met, in renal tubules is required for renoprotection after acute kidney injury  Dong Zhou, Roderick.
Everolimus Inhibits SMC Proliferation Through Transcriptional Repression of Telomerase (A) Cell proliferation assay in primary murine vascular smooth muscle.
SS-31 reduces inflammation after acute renal ischemia.
Volume 56, Issue 3, Pages (September 1999)
Volume 93, Issue 1, (January 2018)
Volume 84, Issue 2, Pages (August 2013)
Volume 84, Issue 5, Pages (November 2013)
Volume 73, Issue 4, Pages (February 2008)
1,25-dihydroxyvitamin D3 inhibits renal interstitial myofibroblast activation by inducing hepatocyte growth factor expression  Yingjian Li, Bradley C.
Volume 76, Issue 10, Pages (November 2009)
Volume 72, Issue 3, Pages (August 2007)
Volume 79, Issue 4, Pages (February 2011)
Renal L-type fatty acid-binding protein mediates the bezafibrate reduction of cisplatin- induced acute kidney injury  K. Negishi, E. Noiri, R. Maeda, D.
Volume 56, Issue 4, Pages (October 1999)
Volume 70, Issue 10, Pages (November 2006)
Volume 122, Issue 2, Pages (February 2002)
Quantitative RT-PCR results of relative gene expression normalized to wild-type (WT) expression levels for the LjMYB14 transgene (A) and genes specific.
The increased cytosolic and nuclear β-catenin in the tubular epithelial cells of 7-d obstructed kidneys is suppressed by recombinant sFRP4. The increased.
Volume 73, Issue 6, Pages (March 2008)
M.-J. Wu, M.-C. Wen, Y.-T. Chiu, Y.-Y. Chiou, K.-H. Shu, M.-J. Tang 
Effects of E2 on levels of phospho-CREB in the DH of OVX females, sham males, and GDX males. Effects of E2 on levels of phospho-CREB in the DH of OVX females,
Chien-Te Lee, Viet M. Huynh, Li-Wen Lai, Yeong-Hau H. Lien 
MEK inhibitor, U0126, attenuates cisplatin-induced renal injury by decreasing inflammation and apoptosis  Sang-Kyung Jo, Won Yong Cho, Su Ah Sung, Hyoung.
ILK knockdown decreases mTOR signaling in PKD kidneys.
Collagen accumulation is reduced with UK
Ciliary abnormalities of jck renal epithelia.
PINCH-1 forms a complex with integrin-linked kinase (ILK) at focal adhesion sites. PINCH-1 forms a complex with integrin-linked kinase (ILK) at focal adhesion.
Representative photomicrographs of immunohistochemical staining for Wilms’ tumor 1 (WT1) and cleaved caspase-3 in mouse kidney sections at 10, 20, and.
Ganesan Ramesh, W. Brian Reeves  Kidney International 
Volume 76, Issue 8, Pages (October 2009)
ONC201 activates the ISR. ONC201 activates the ISR. (A) Western blotting analysis for ATF4, CHOP, ATF3, and TRB3 on lysates from HCT116 cells cultured.
CO-1686 does not inhibit WT EGFR signaling in vivo and is active in EGFR-mutant transgenic mouse lung cancer models. CO-1686 does not inhibit WT EGFR signaling.
Volume 21, Issue 2, Pages (February 2013)
(Top) Micrographs of SNAIL-HA and mock-infected cells.
TRAF6 exacerbates I/R-induced neuronal death.
Analysis of mRNA and protein levels of Loricrin, COMP, CXCL9, KRT19, and CYP 3A5 genes in OSFs compared with normal controls. Analysis of mRNA and protein.
NT157 treatment inhibits LNCaP xenograft growth and delays castration-resistant progression. NT157 treatment inhibits LNCaP xenograft growth and delays.
Enhanced expression of Cap43 gene by nickel in breast cancer cell lines. Enhanced expression of Cap43 gene by nickel in breast cancer cell lines. Expression.
Presentation transcript:

Inhibition of ILK by QLT-0267 reduces β-catenin accumulation and inhibits Snail1 expression in obstructive nephropathy. Inhibition of ILK by QLT-0267 reduces β-catenin accumulation and inhibits Snail1 expression in obstructive nephropathy. (A) Representative Western blot demonstrates that QLT-0267 administration significantly reduced β-catenin abundance in the obstructed kidney at 7 d after UUO. Numbers denote each individual mouse in a given group. (B) Graphic presentation shows the relative abundance of β-catenin in various groups as indicated. Data are means ± SEM of five animals per group. *P < 0.05 versus sham controls; †P < 0.05 versus vehicle controls. (C through E) Immunohistochemical staining shows β-catenin localization in different groups. (C) Sham controls. (D) UUO 7d. (E) UUO 7d injected with QLT-0267. Bar = 40 μm. Arrowheads indicate nuclear staining of β-catenin. (F) Quantitative determination of renal Snail1 mRNA levels by real-time RT-PCR in various groups as indicated. Relative renal Snail1 mRNA levels (fold induction versus sham controls) were presented. *P < 0.05 versus sham controls; †P < 0.05 versus vehicle controls. The dosages of QLT-0267 (mg/kg body wt) are given. Yingjian Li et al. JASN 2009;20:1907-1918 ©2009 by American Society of Nephrology