ROCK2 regulates TGF-β-induced expression of CTGF and profibrotic genes via NF-κB and cytoskeleton dynamics in mesangial cells.
Yosuke NagaiKeiichiro MatobaDaiji KawanamiYusuke TakedaTomoyo AkamineSho IshizawaYasushi KanazawaTamotsu YokotaKazunori UtsunomiyaRimei NishimuraPublished in: American journal of physiology. Renal physiology (2019)
The small GTPase Rho and its effector Rho kinase (ROCK) are involved in the pathogenesis of diabetic kidney disease. Rho kinase has two isoforms: ROCK1 and ROCK2. However, it remains unclear which is mainly involved in the progression of diabetic glomerulosclerosis and the regulation of profibrotic mediators. Glomeruli isolated from type 2 diabetic db/db mice demonstrated increased gene expression of transforming growth factor (TGF)-β and its downstream profibrotic mediators. Chemical inhibition of ROCK suppressed the expression of profibrotic mediators in both isolated glomeruli and cultured mesangial cells. An investigation of mechanisms underlying this observation revealed activated ROCK functions through the phosphorylation of JNK and Erk and the nuclear translocation of NF-κB via actin dynamics. Knockdown by siRNA against ROCK1 and ROCK2 showed that ROCK2 but not ROCK1 controls this fibrotic machinery. Further in vivo experiments showed that ROCK2 activity in the renal cortex of db/db mice was elevated compared with control db/m mice. Importantly, oral administration of ROCK2 inhibitor attenuated renal ROCK2 activity, albuminuria, and glomerular fibrosis in db/db mice. These observations indicate that ROCK2 is a key player in the development of diabetic renal injury. Glomerular ROCK2 may be a potential therapeutic target for the treatment of diabetic kidney disease.
Keyphrases
- transforming growth factor
- gene expression
- type diabetes
- signaling pathway
- protein kinase
- epithelial mesenchymal transition
- cell death
- genome wide
- risk assessment
- dna methylation
- climate change
- drug delivery
- adipose tissue
- metabolic syndrome
- tyrosine kinase
- long non coding rna
- endoplasmic reticulum stress
- replacement therapy
- smoking cessation
- wild type