Progress in the application of mesenchymal stem cells to attenuate apoptosis in diabetic kidney disease

Ping Nie1, Wei Qin1, Wei-Chen Nie2

  • 1Department of Nephropathy, The Second Hospital of Jilin University, Changchun 130041, Jilin Province, China.

PubMed

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.