TY - JOUR
T1 - Inhibition of MLL1-menin interaction attenuates renal fibrosis in obstructive nephropathy
AU - Zou, Jianan
AU - Yu, Chao
AU - Zhang, Chunyun
AU - Guan, Yingjie
AU - Zhang, Yunhe
AU - Tolbert, Evelyn
AU - Zhang, Wei
AU - Zhao, Ting
AU - Bayliss, George
AU - Li, Xiaogang
AU - Ye, Zhibin
AU - Zhuang, Shougang
N1 - Funding Information:
This work was supported by the US National Institutes of Health (2R01DK08506505A1to S.Z), the National Natural Science Foundation of China (81830021 and 82070700 to S.Z; 822008181 to C.Y), and National key R&D Program of China (2018YFA0108802 to S.Z.).
Publisher Copyright:
© 2022 Federation of American Societies for Experimental Biology.
PY - 2023/1
Y1 - 2023/1
N2 - Mixed lineage leukemia 1 (MLL1), a histone H3 lysine 4 (H3K4) methyltransferase, exerts its enzymatic activity by interacting with menin and other proteins. It is unclear whether inhibition of the MLL1-menin interaction influences epithelial-mesenchymal transition (EMT), renal fibroblast activation, and renal fibrosis. In this study, we investigated the effect of disrupting MLL1-menin interaction on those events and mechanisms involved in a murine model of renal fibrosis induced by unilateral ureteral obstruction (UUO), in cultured mouse proximal tubular cells and renal interstitial fibroblasts. Injury to the kidney increased the expression of MLL1 and menin and H3K4 monomethylation (H3K4me1); MLL1 and menin were expressed in renal epithelial cells and renal interstitial fibroblasts. Inhibition of the MLL1-menin interaction by MI-503 administration or siRNA-mediated silencing of MLL1 attenuated UUO-induced renal fibrosis, and reduced expression of α-smooth muscle actin (α-SMA) and fibronectin. These treatments also inhibited UUO-induced expression of transcription factors Snail and Twist and transforming growth factor β1 (TGF-β1) while expression of E-cadherin was preserved. Moreover, treatment with MI-503 and transfection with either MLL siRNA or menin siRNA inhibited TGF-β1-induced upregulation of α-SMA, fibronectin and Snail, phosphorylation of Smad3 and AKT, and downregulation of E-cadherin in cultured renal epithelial cells. Finally, MI-503 was effective in abrogating serum or TGFβ1-induced transformation of renal interstitial fibroblasts to myofibroblasts in vitro. Taken together, these results suggest that targeting disruption of the MLL1-menin interaction attenuates renal fibrosis through inhibition of partial EMT and renal fibroblast activation.
AB - Mixed lineage leukemia 1 (MLL1), a histone H3 lysine 4 (H3K4) methyltransferase, exerts its enzymatic activity by interacting with menin and other proteins. It is unclear whether inhibition of the MLL1-menin interaction influences epithelial-mesenchymal transition (EMT), renal fibroblast activation, and renal fibrosis. In this study, we investigated the effect of disrupting MLL1-menin interaction on those events and mechanisms involved in a murine model of renal fibrosis induced by unilateral ureteral obstruction (UUO), in cultured mouse proximal tubular cells and renal interstitial fibroblasts. Injury to the kidney increased the expression of MLL1 and menin and H3K4 monomethylation (H3K4me1); MLL1 and menin were expressed in renal epithelial cells and renal interstitial fibroblasts. Inhibition of the MLL1-menin interaction by MI-503 administration or siRNA-mediated silencing of MLL1 attenuated UUO-induced renal fibrosis, and reduced expression of α-smooth muscle actin (α-SMA) and fibronectin. These treatments also inhibited UUO-induced expression of transcription factors Snail and Twist and transforming growth factor β1 (TGF-β1) while expression of E-cadherin was preserved. Moreover, treatment with MI-503 and transfection with either MLL siRNA or menin siRNA inhibited TGF-β1-induced upregulation of α-SMA, fibronectin and Snail, phosphorylation of Smad3 and AKT, and downregulation of E-cadherin in cultured renal epithelial cells. Finally, MI-503 was effective in abrogating serum or TGFβ1-induced transformation of renal interstitial fibroblasts to myofibroblasts in vitro. Taken together, these results suggest that targeting disruption of the MLL1-menin interaction attenuates renal fibrosis through inhibition of partial EMT and renal fibroblast activation.
KW - epithelial-mesenchymal transition
KW - menin
KW - mixed lineage leukemia 1
KW - renal fibrosis
KW - renal interstitial fibroblasts
UR - http://www.scopus.com/inward/record.url?scp=85144586152&partnerID=8YFLogxK
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U2 - 10.1096/fj.202100634RRR
DO - 10.1096/fj.202100634RRR
M3 - Article
C2 - 36527439
AN - SCOPUS:85144586152
SN - 0892-6638
VL - 37
JO - FASEB Journal
JF - FASEB Journal
IS - 1
M1 - e22712
ER -