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Updated: Jan 22, 2026

An Effective Mouse Model of Unilateral Renal Ischemia-Reperfusion Injury
Published on: July 15, 2021
Biochemical and histological effects of embryonic stem cells in a mouse model of renal failure
Gustavo Jesus Vazquez-Zapien1, Adriana Martinez-Cuazitl, Laura Susana Rangel-Cova
1Laboratorio de Biología Celular y Tisular, Escuela Militar de Medicina, Centro Militar de Ciencias de la Salud, Secretaría de la Defensa Nacional, Ciudad de México, México; mmcmaribel@gmail.com.
Abstract:
Kidney diseases are a global public health problem. Despite significant advances in the understanding of renal failure (RF) and replacement therapies, this condition carries a series of complications and the life's quality of patients decreases. Differentiation capability of stem cells and their beneficial effects when they are implanted in animal models have been reported. Therefore, this work aimed to induce a long-term RF in mice, evaluating the biochemical and histological effects after implanting mouse embryonic stem cells (mESC). Mice were subjected to renal failure induction (RFI) employing cisplatin, subsequently received intraperitoneal (i.p.) injections of salt solution (control group, n=19) or 50 000 mESC (experimental group, n=19) at 24 hours, 7 days, and 13 days post-RFI. Ten animals in each group were used to analyze functional damage through serum biochemical analysis, and the mortality. For histopathological examination, three animals of each group were sacrificed at 5, 10, and 20 days post-RFI, analyzing the tubular system and glomeruli. Both groups showed blood urea nitrogen (BUN) and creatinine elevation three days post-RFI. Accumulated mortality was lower in the experimental group, presenting statistical significance. Respect to histopathological effects, the control group showed tubular dilatation, segmental focal glomerulosclerosis data, and collapsed glomeruli, while in the experimental group, glomerulosclerosis or collapsed glomeruli were not observed, evidencing regenerative data as characterized by large nuclei with prominent and binucleate nucleoli. In conclusion, mESC implant in mice with RFI significantly decreased the mortality, avoiding a greater histological deterioration related to the disease.
Insights
Mouse embryonic stem cell (mESC) implantation in mice with induced renal failure (RF) significantly reduced mortality and prevented severe kidney damage. This study highlights the regenerative potential of mESC in treating kidney disease.
Area of Science:
- Nephrology
- Stem Cell Biology
- Regenerative Medicine
Background:
- Kidney diseases represent a significant global health burden, leading to complications and reduced quality of life.
- Stem cells exhibit differentiation capabilities and have shown promise in animal models of disease.
- Current renal failure (RF) treatments have limitations, necessitating exploration of novel therapeutic approaches.
Purpose of the Study:
- To investigate the therapeutic effects of mouse embryonic stem cell (mESC) transplantation in a murine model of long-term renal failure (RF).
- To evaluate the biochemical and histological outcomes following mESC implantation in mice with cisplatin-induced RF.
Main Methods:
- Long-term RF was induced in mice using cisplatin.
- Mice received intraperitoneal injections of either saline (control) or 50,000 mESC at 24 hours, 7 days, and 13 days post-renal failure induction (RFI).
- Serum biochemical analysis, mortality rates, and histopathological examinations of renal tissues (tubular system and glomeruli) were performed.
Main Results:
- Both groups exhibited elevated blood urea nitrogen (BUN) and creatinine levels three days post-RFI.
- The mESC-treated group showed significantly lower accumulated mortality compared to the control group.
- Histopathological analysis revealed tubular dilatation, glomerulosclerosis, and collapsed glomeruli in controls, whereas the mESC group displayed regenerative signs without glomerulosclerosis or collapsed glomeruli.
Conclusions:
- Implantation of mESC in mice with induced RF significantly reduced mortality rates.
- mESC treatment effectively mitigated severe histological deterioration, including glomerulosclerosis and tubular damage.
- These findings suggest that mESC holds therapeutic potential for mitigating the progression of kidney disease.
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