Progress in the application of mesenchymal stem cells to attenuate apoptosis in diabetic kidney disease
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Updated: Sep 18, 2025

Prospective, Randomized, and Controlled Study of a Human Umbilical Cord Mesenchymal Stem Cell Injection for Treating Diabetic Foot Ulcers
Published on: March 3, 2023
Ping Nie1, Wei Qin1, Wei-Chen Nie2
1Department of Nephropathy, The Second Hospital of Jilin University, Changchun 130041, Jilin Province, China.
Abstract:
Diabetic kidney disease (DKD) has a high incidence and mortality rate and lacks effective preventive and therapeutic methods. Apoptosis is one of the main reasons for the occurrence and development of DKD. Mesenchymal stem cells (MSCs) have shown great promise in tissue regeneration for DKD treatment and have protective effects against DKD, including decreased blood glucose and urinary protein levels and improved renal function. MSCs can directly differentiate into kidney cells or act via paracrine mechanisms to reduce apoptosis in DKD by modulating signaling pathways. MSC-derived extracellular vesicles (MSC-EVs) mitigate apoptosis and DKD-related symptoms by transferring miRNAs to target cells or organs. However, studies on the regulatory mechanisms of MSCs and MSC-EVs in apoptosis in DKD are insufficient. This review comprehensively examines the mechanisms of apoptosis in DKD and research progress regarding the roles of MSCs and MSC-EVs in the disease process.
Insights
Mesenchymal stem cells (MSCs) and their extracellular vesicles (MSC-EVs) show promise in treating diabetic kidney disease (DKD) by reducing apoptosis. Further research is needed to fully understand their regulatory mechanisms in DKD.
Area of Science:
- Nephrology
- Regenerative Medicine
- Cell Biology
Background:
- Diabetic kidney disease (DKD) presents a significant health challenge with high mortality and limited treatment options.
- Apoptosis, or programmed cell death, is a key driver in the progression of DKD.
- Mesenchymal stem cells (MSCs) offer potential therapeutic benefits for DKD through tissue regeneration and protective effects.
Purpose of the Study:
- To review the mechanisms of apoptosis in diabetic kidney disease.
- To examine the current research on the therapeutic roles of MSCs and MSC-derived extracellular vesicles (MSC-EVs) in DKD.
- To highlight the need for further investigation into MSC and MSC-EV regulatory pathways in DKD.
Main Methods:
- Comprehensive literature review of studies on apoptosis in DKD.
- Analysis of research on MSC transplantation and paracrine effects in DKD models.
- Evaluation of studies investigating MSC-EVs, including miRNA transfer, in DKD treatment.
Main Results:
- MSCs demonstrate protective effects in DKD by improving renal function, reducing blood glucose, and lowering urinary protein levels.
- MSCs and MSC-EVs can mitigate apoptosis in DKD through direct differentiation or paracrine signaling, including miRNA modulation.
- Existing research indicates MSCs and MSC-EVs are promising for DKD therapy, but mechanisms require deeper exploration.
Conclusions:
- Apoptosis is a critical factor in DKD pathogenesis, and MSC-based therapies show significant potential for mitigating this process.
- MSC-EVs offer a cell-free therapeutic strategy for DKD by delivering bioactive molecules that reduce apoptosis.
- Further research is essential to elucidate the intricate mechanisms of MSCs and MSC-EVs in combating DKD and to optimize their clinical application.
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