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Updated: Sep 7, 2025
A Mouse 5/6th Nephrectomy Model That Induces Experimental Uremic Cardiomyopathy
Published on: November 7, 2017
Cathepsin K Deficiency Prevented Kidney Damage and Dysfunction in Response to 5/6 Nephrectomy Injury in Mice With or
Xueling Yue1,2, Limei Piao1, Hailong Wang1
1Department of Cardiology and Hypertension, Yanbian University Hospital, Yanji, Jilin, People's Republic of China (X.Y., L.P., H.W., Z.H., X.M., Y.W., S.X., X.W.C.).
Background:
Chronic psychological stress is a risk factor for kidney disease, including kidney dysfunction and hypertension. Lysosomal CatK (cathepsin K) participates in various human pathobiologies. We investigated the role of CatK in kidney remodeling and hypertension in response to 5/6 nephrectomy injury in mice with or without chronic stress.
Methods:
Male 7-week-old WT (wild type; CatK+/+) and CatK-deficient (CatK-/-) mice that were or were not subjected to chronic stress underwent 5/6 nephrectomy. At 8 weeks post-stress/surgery, the stress was observed to have accelerated injury-induced glomerulosclerosis, proteinuria, and blood pressure elevation.
Results:
Compared with the nonstressed mice, the stressed mice showed increased levels of TLR (Toll-like receptor)-2/4, p22phox, gp91phox, CatK, MMP (matrix metalloproteinase)-2/9, collagen type I and III genes, PPAR-γ (peroxisome proliferator-activated receptor-gamma), NLRP-3 (NOD-like receptor thermal protein domain associated protein 3), p21, p16, and cleaved caspase-8 proteins, podocyte foot process effacement, macrophage accumulation, apoptosis, and decreased levels of Bcl-2 (B cell lymphoma 2) and Sirt1, as well as decreased glomerular desmin expression in the kidneys. These harmful changes were retarded by the genetic or pharmacological inhibition of CatK. Consistently, CatK inhibition ameliorated 5/6 nephrectomy-related kidney injury and dysfunction. In mesangial cells, CatK silencing or overexpression, respectively, reduced or increased the PPAR-γ and cleaved caspase-8 protein levels, providing evidence and a mechanistic explanation of CatK's involvement in PPAR-γ/caspase-8-mediated cell apoptosis in response to superoxide and stressed serum.
Conclusions:
These results demonstrate that CatK plays an essential role in kidney remodeling and hypertension in response to 5/6 nephrectomy or stress, possibly via a reduction of glomerular inflammation, apoptosis, and fibrosis, suggesting a novel therapeutic strategy for controlling kidney injury in mice under chronic psychological stress conditions.
Insights
Chronic stress accelerates kidney injury and hypertension. Cathepsin K (CatK) inhibition protected against this damage, suggesting CatK as a therapeutic target for stress-induced kidney disease.
Area of Science:
- Nephrology
- Molecular Biology
- Stress Physiology
Background:
- Chronic psychological stress is a significant risk factor for kidney disease, including kidney dysfunction and hypertension.
- Lysosomal Cathepsin K (CatK) is implicated in various human pathologies.
Purpose of the Study:
- To investigate the role of CatK in kidney remodeling and hypertension following 5/6 nephrectomy injury in mice subjected to chronic stress.
- To evaluate the therapeutic potential of CatK inhibition in mitigating stress-exacerbated kidney damage.
Main Methods:
- Male wild-type (WT) and CatK-deficient (CatK-/-) mice were subjected to 5/6 nephrectomy, with or without chronic stress.
- Assessment of kidney injury markers, blood pressure, and molecular changes at 8 weeks post-surgery and stress.
Main Results:
- Chronic stress accelerated glomerulosclerosis, proteinuria, and hypertension post-nephrectomy.
- Stressed mice exhibited increased markers of inflammation, oxidative stress, apoptosis, and fibrosis, which were attenuated by CatK inhibition.
- CatK inhibition ameliorated kidney injury and dysfunction, with CatK silencing/overexpression affecting PPAR-γ and caspase-8 levels in mesangial cells.
Conclusions:
- Cathepsin K (CatK) is crucial in kidney remodeling and hypertension under stress and 5/6 nephrectomy injury.
- CatK inhibition reduces glomerular inflammation, apoptosis, and fibrosis, offering a potential therapeutic strategy for stress-induced kidney disease.
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