TGF-β/Smad signaling in chronic kidney disease: Exploring post-translational regulatory perspectives (Review)

被引:11
作者
Li, Jianchun [1 ,2 ]
Zou, Yuanxia [1 ,2 ]
Kantapan, Jiraporn [1 ]
Su, Hongwei [3 ]
Wang, Li [2 ]
Dechsupa, Nathupakorn [1 ]
机构
[1] Chiang Mai Univ, Fac Associated Med Sci, Dept Radiol Technol, Mol Imaging & Therapy Res Unit, 110 Intawaroros Rd, Chiang Mai 50200, Thailand
[2] Southwest Med Univ, Affiliated Tradit Chinese Med Hosp, Res Ctr Integrated Tradit Chinese & Western Med, 182 Chunhui Rd, Luzhou 646000, Sichuan, Peoples R China
[3] Southwest Med Univ, Affiliated Tradit Chinese Med Hosp, Dept Urol, Luzhou 646000, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
chronic kidney disease; TGF-beta; Smads; post-translational modification; fibrosis; TO-MESENCHYMAL TRANSITION; RENAL FIBROSIS; BETA RECEPTOR; TUBULOINTERSTITIAL FIBROSIS; MYOFIBROBLAST TRANSITION; C-JUN; PROTEIN; SMAD7; ACTIVATION; CELLS;
D O I
10.3892/mmr.2024.13267
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The TGF-beta/Smad signaling pathway plays a pivotal role in the onset of glomerular and tubulointerstitial fibrosis in chronic kidney disease (CKD). The present review delves into the intricate post-translational modulation of this pathway and its implications in CKD. Specifically, the impact of the TGF-beta/Smad pathway on various biological processes was investigated, encompassing not only renal tubular epithelial cell apoptosis, inflammation, myofibroblast activation and cellular aging, but also its role in autophagy. Various post-translational modifications (PTMs), including phosphorylation and ubiquitination, play a crucial role in modulating the intensity and persistence of the TGF-beta/Smad signaling pathway. They also dictate the functionality, stability and interactions of the TGF-beta/Smad components. The present review sheds light on recent findings regarding the impact of PTMs on TGF-beta receptors and Smads within the CKD landscape. In summary, a deeper insight into the post-translational intricacies of TGF-beta/Smad signaling offers avenues for innovative therapeutic interventions to mitigate CKD progression. Ongoing research in this domain holds the potential to unveil powerful antifibrotic treatments, aiming to preserve renal integrity and function in patients with CKD.
引用
收藏
页码:143 / 2024
页数:13
相关论文
共 170 条
[121]   TGF-β1 is involved in senescence-related pathways in glomerular endothelial cells via p16 translocation and p21 induction [J].
Ueda, Sayo ;
Tominaga, Tatsuya ;
Ochi, Arisa ;
Sakurai, Akiko ;
Nishimura, Kenji ;
Shibata, Eriko ;
Wakino, Shu ;
Tamaki, Masanori ;
Nagai, Kojiro .
SCIENTIFIC REPORTS, 2021, 11 (01)
[122]   Suppression of microRNA-29 Expression by TGF-β1 Promotes Collagen Expression and Renal Fibrosis [J].
Wang, Bo ;
Komers, Radko ;
Carew, Rosemarie ;
Winbanks, Catherine E. ;
Xu, Bei ;
Herman-Edelstein, Michal ;
Koh, Philip ;
Thomas, Merlin ;
Jandeleit-Dahm, Karin ;
Gregorevic, Paul ;
Cooper, Mark E. ;
Kantharidis, Phillip .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2012, 23 (02) :252-265
[123]   POH1 contributes to hyperactivation of TGF-β signaling and facilitates hepatocellular carcinoma metastasis through deubiquitinating TGF-β receptors and caveolin-1 [J].
Wang, Boshi ;
Xu, Xiaoli ;
Yang, Zhaojuan ;
Zhang, Li ;
Liu, Yun ;
Ma, Aihui ;
Xu, Guiqin ;
Tang, Ming ;
Jing, Tiantian ;
Wu, Lin ;
Liu, Yongzhong .
EBIOMEDICINE, 2019, 41 :320-332
[124]   Smad3 promotes AKI sensitivity in diabetic mice via interaction with p53 and induction of NOX4-dependent ROS production [J].
Wang, Jia-Nan ;
Yang, Qin ;
Yang, Chen ;
Cai, Yu-Ting ;
Xing, Tian ;
Gao, Li ;
Wang, Fang ;
Chen, Xin ;
Liu, Xue-Qi ;
He, Xiao-Yan ;
Wei, Biao ;
Jiang, Ling ;
Li, Chao ;
Jin, Juan ;
Wen, Jia-Gen ;
Ma, Tao-Tao ;
Chen, Hai-Yong ;
Li, Jun ;
Meng, Xiao-Ming .
REDOX BIOLOGY, 2020, 32
[125]   Ferroptosis, a new target for treatment of renal injury and fibrosis in a 5/6 nephrectomy-induced CKD rat model [J].
Wang, Jingyu ;
Wang, Yaqing ;
Liu, Yi ;
Cai, Xintian ;
Huang, Xin ;
Fu, Wenjing ;
Wang, Lei ;
Qiu, Lihua ;
Li, Junying ;
Sun, Li .
CELL DEATH DISCOVERY, 2022, 8 (01)
[126]   Flavin containing monooxygenase 2 regulates renal tubular cell fibrosis and paracrine secretion via SMURF2 in AKI-CKD transformation [J].
Wang, Longfei ;
Zha, Hongchu ;
Huang, Jing ;
Shi, Lang .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2023, 52 (05)
[127]   TGF-β/Smad3 signalling regulates the transition of bone marrow-derived macrophages into myofibroblasts during tissue fibrosis [J].
Wang, Shuang ;
Meng, Xiao-Ming ;
Ng, Yee-Yung ;
Ma, Frank Y. ;
Zhou, Shuang ;
Zhang, Yang ;
Yang, Chen ;
Huang, Xiao-Ru ;
Xiao, Jun ;
Wang, Ying-Ying ;
Ka, Shuk-Man ;
Tang, Yong-Jiang ;
Chung, Arthur C. K. ;
To, Ka-Fai ;
Nikolic-Paterson, David J. ;
Lan, Hui-Yao .
ONCOTARGET, 2016, 7 (08) :8809-8822
[128]   SARS-CoV-2 N Protein Induces Acute Kidney Injury via Smad3-Dependent G1 Cell Cycle Arrest Mechanism [J].
Wang, Wenbiao ;
Chen, Junzhe ;
Hu, Dingwen ;
Pan, Pan ;
Liang, Liying ;
Wu, Wenjing ;
Tang, Ying ;
Huang, Xiao R. ;
Yu, Xueqing ;
Wu, Jianguo ;
Lan, Hui Y. .
ADVANCED SCIENCE, 2022, 9 (03)
[129]   Signaling mechanism of TGF-βl in prevention of renal inflammation:: Role of Smad7 [J].
Wang, WS ;
Huang, XR ;
Li, AG ;
Liu, F ;
Li, JH ;
Truong, LD ;
Wang, XJ ;
Lan, HY .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (05) :1371-1383
[130]   Regulation of transforming growth factor-β signalling by SUMOylation and its role in fibrosis [J].
Wang, Xinyi ;
Liu, Ting ;
Huang, Yifei ;
Dai, Yifeng ;
Lin, Hui .
OPEN BIOLOGY, 2021, 11 (11)