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Updated: May 17, 2026

08:21
A Modified Two Kidney One Clip Mouse Model of Renin Regulation in Renal Artery Stenosis
Published on: October 26, 2020
Mesenchymal stem cells and endothelial progenitor cells decrease renal injury in experimental swine renal artery
Xiang-Yang Zhu1, Victor Urbieta-Caceres, James D Krier
1Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota 55905, USA.
Stem Cells (Dayton, Ohio)
|October 26, 2012
Summary
Endothelial progenitor cells (EPC) and mesenchymal stem cells (MSC) both aid kidney repair in renovascular disease. MSCs offer slightly better functional recovery by reducing inflammation and cell death, while EPCs boost growth factors.
Area of Science:
- Regenerative Medicine
- Nephrology
- Vascular Biology
Background:
- Renovascular disease impairs kidney function.
- Endothelial progenitor cells (EPC) and mesenchymal stem cells (MSC) show promise in tissue repair.
- Understanding cell-specific mechanisms in renovascular disease is crucial.
Purpose of the Study:
- To test if EPCs and MSCs protect kidneys in renovascular disease via distinct pathways.
- To compare the efficacy of EPCs and MSCs in improving kidney hemodynamics and function post-stenosis.
Main Methods:
- Characterization of peripheral blood EPCs and adipose-derived MSCs.
- Assessment of kidney hemodynamics and function in pigs with renal artery stenosis (RAS) treated with EPCs, MSCs, or vehicle.
- Ex vivo evaluation of kidney disease mechanisms and cellular stress pathways (ER stress, apoptosis).
Main Results:
- Both EPCs and MSCs improved renal blood flow similarly in RAS.
- MSCs significantly enhanced glomerular filtration rate compared to EPCs.
- EPCs increased renal growth factors and decreased oxidative stress.
- MSCs more effectively reduced renal inflammation, ER stress, and apoptosis, including caspase-3 and CHOP expression.
Conclusions:
- EPCs and MSCs mitigate kidney injury in renovascular disease through different mechanisms.
- MSCs demonstrated a slightly superior improvement in renal function.
- Cell selection should be guided by the specific pathophysiology of kidney injury in renovascular disease.
