473-P: HDAC Inhibition Augments TGF-ß-Induced JNK Activation, CTGF Expression, and NF-E2 Degradation Promoting Profibrotic Signaling in Renal Proximal Tubules

Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 473-P
Author(s):  
JIA LI ◽  
MADHAVI JAGDISH RANE ◽  
LU CAI ◽  
YI TAN
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2016 ◽  
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He Tian ◽  
Ping Zhang ◽  
Zhen-Xing Zhang

2019 ◽  
Vol 4 (7) ◽  
pp. S216
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M. Nakamura ◽  
N. Satoh ◽  
T. Mizuno ◽  
Y. Sato ◽  
...  

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pp. 80-85 ◽  
Author(s):  
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Bok Yun Kang ◽  
Hyun Joong Yoon ◽  
Eun Mi Park ◽  
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Vol 20 (4) ◽  
Author(s):  
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Brian Westwood ◽  
David Averill ◽  
Jorge Figueroa ◽  
Carlos Ferrario ◽  
...  

2021 ◽  
Author(s):  
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Lei Cai ◽  
Dien Ye ◽  
Hisashi Sawada ◽  
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...  

AGT (Angiotensinogen) is the unique substrate of the renin-angiotensin system. Liver is the primary source of circulating AGT. The present study determined whether hepatocyte-derived AGT regulates renal AGT accumulation by injecting ASO (antisense oligonucleotides) targeting hepatocyte-derived AGT (GalNAc AGT ASO) into female cynomolgus monkeys. Hepatocyte-specific inhibition of AGT led to profound reductions of plasma AGT concentrations. AGT protein in S1 and S2 of renal proximal tubules was greatly diminished by GalNAc AGT ASO. Given the similarity between nonhuman primates and human, our findings support the notion that renal AGT is predominantly derived from liver, and liver regulates renal angiotensin II production in humans.


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