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Published on: March 3, 2023
Evaluation of the Effect of Different Mesenchymal Stem Cell Microvesicles on Diabetic Wound Healing
Cemal Alper Kemaloğlu1, Ömer Taşkın2, Zeynep Burçin Gönen3
1Department of Plastic, Reconstructive and Aesthetic Surgery, Memorial Ankara Hospital, Ankara, Türkiye.
Objective:
Mesenchymal stem cell (MSC)-derived microvesicles play a pivotal role in the regenerative cascade of wound healing. This study aimed to comparatively evaluate the therapeutic potential of microvesicles isolated from different MSC sources in the healing of diabetic cutaneous wounds.
Materials And Methods:
Forty Wistar albino rats were randomly assigned to four experimental groups (n=10 per group). Following the induction of diabetes and the creation of full-thickness circular dorsal skin defects, each group received a distinct treatment: Group 1 received saline (control), Group 2 received adipose-derived stem cell microvesicles (ADSC-MVs), Group 3 received umbilical cord-derived stem cell microvesicles (UCDSC-MVs), and Group 4 received bone marrow-derived stem cell microvesicles (BMDSC-MVs). Outcomes related to re-epithelialization, neovascularization, and collagen matrix formation were evaluated both macroscopically and histologically.
Results:
The microvesicle-treated groups demonstrated faster wound closure and improved collagen fiber alignment compared with the control group. Angiogenic activity was increased in all treatment groups, with the most pronounced effects observed in the UCDSC-MVs group. Notably, the UCDSC-MVs group exhibited a significantly greater epithelial tongue length than the control group on postoperative days 3 and 14 (p=0.008 and p<0.001, respectively).
Conclusion:
These findings indicate that UCDSC-MVs possess a superior capacity to promote re-epithelialization and may represent an effective cell-free therapeutic approach for diabetic wound repair.
Insights
Umbilical cord-derived stem cell microvesicles (UCDSC-MVs) significantly enhance diabetic wound healing by promoting re-epithelialization and collagen formation. This study highlights UCDSC-MVs as a promising cell-free therapy for diabetic cutaneous wound repair.
Area of Science:
- Regenerative Medicine
- Wound Healing Biology
- Stem Cell Therapeutics
Background:
- Mesenchymal stem cell (MSC)-derived microvesicles are crucial for wound regeneration.
- Diabetic cutaneous wounds present a significant clinical challenge due to impaired healing.
- Evaluating different MSC sources for microvesicle-based therapies is essential for optimizing diabetic wound repair.
Purpose of the Study:
- To comparatively assess the therapeutic efficacy of microvesicles from adipose-derived stem cells (ADSC-MVs), umbilical cord-derived stem cells (UCDSC-MVs), and bone marrow-derived stem cells (BMDSC-MVs) in healing diabetic cutaneous wounds.
- To determine the optimal MSC source for microvesicle-based wound healing therapies.
Main Methods:
- Forty Wistar albino rats with induced diabetes and dorsal skin defects were divided into four groups: control (saline), ADSC-MVs, UCDSC-MVs, and BMDSC-MVs.
- Macroscopic and histological evaluations assessed re-epithelialization, neovascularization, and collagen matrix formation.
- Statistical analysis compared treatment outcomes at specific postoperative time points.
Main Results:
- All microvesicle treatments accelerated wound closure and improved collagen alignment compared to controls.
- Increased angiogenic activity was observed across all treatment groups, with UCDSC-MVs showing the most significant effect.
- UCDSC-MVs demonstrated significantly enhanced epithelial tongue length on postoperative days 3 and 14 (p=0.008 and p<0.001, respectively).
Conclusions:
- Umbilical cord-derived stem cell microvesicles exhibit superior potential in promoting re-epithelialization for diabetic wound healing.
- UCDSC-MVs represent a promising cell-free therapeutic strategy for managing complex diabetic wounds.
- Further research into UCDSC-MVs could lead to novel treatments for chronic wound conditions.
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Mesenchymal Stem Cells
Clinical Applications of Epidermal Stem Cells

