Human decellularized dermal matrix seeded with adipose-derived stem cells enhances wound healing in a murine model: Experimental study.
Abstract
[OBJECTIVE] Full-thickness cutaneous wounds treated with split-thickness skin grafts often result in unaesthetic and hypertrophic scars. Dermal substitutes are currently used together with skin grafts in a single treatment to reconstruct the dermal layer of the skin, resulting in improved quality of scars. Adipose-derived stem cells (ASCs) have been described to enhance wound healing through structural and humoral mechanisms. In this study, we investigate the compatibility of xenogen-free isolated human ASCs seeded on human acellular dermal matrix (Glyaderm®) in a murine immunodeficient wound model.
[METHODS] Adipose tissue was obtained from abdominal liposuction, and stromal cells were isolated mechanically and cultured xenogen-free in autologous plasma-supplemented medium. Glyaderm® discs were seeded with EGFP-transduced ASCs, and implanted on 8 mm full-thickness dorsal wounds in an immunodeficient murine model, in comparison to standard Glyaderm® discs. Re-epithelialization rate, granulation thickness and vascularity were assessed by histology on days 3, 7 and 12. Statistical analysis was conducted using the Wilcoxon signed-rank test. EGFP-staining allowed for tracking of the ASCs in vivo. Hypoxic culture of the ASCs was performed to evaluate cytokine production.
[RESULTS] ASCs were characterized with flowcytometric analysis and differentiation assay. EGFP-tranduction resulted in 95% positive cells after sorting. Re-epithelialization in the ASC-seeded Glyaderm® side was significantly increased, resulting in complete wound healing in 12 days. Granulation thickness and vascularization were significantly increased during early wound healing. EGFP-ASCs could be retrieved by immunohistochemistry in the granulation tissue in early wound healing, and lining vascular structures in later stages.
[CONCLUSION] Glyaderm® is an effective carrier to deliver ASCs in full-thickness wounds. ASC-seeded Glyaderm® significantly enhances wound healing compared to standard Glyaderm®. The results of this study encourage clinical trials for treatment of full-thickness skin defects. Furthermore, xenogen-free isolation and autologous plasma-augmented culture expansion of ASCs, combined with the existing clinical experience with Glyaderm®, aid in simplifying the necessary procedures in a GMP-laboratory setting.
[METHODS] Adipose tissue was obtained from abdominal liposuction, and stromal cells were isolated mechanically and cultured xenogen-free in autologous plasma-supplemented medium. Glyaderm® discs were seeded with EGFP-transduced ASCs, and implanted on 8 mm full-thickness dorsal wounds in an immunodeficient murine model, in comparison to standard Glyaderm® discs. Re-epithelialization rate, granulation thickness and vascularity were assessed by histology on days 3, 7 and 12. Statistical analysis was conducted using the Wilcoxon signed-rank test. EGFP-staining allowed for tracking of the ASCs in vivo. Hypoxic culture of the ASCs was performed to evaluate cytokine production.
[RESULTS] ASCs were characterized with flowcytometric analysis and differentiation assay. EGFP-tranduction resulted in 95% positive cells after sorting. Re-epithelialization in the ASC-seeded Glyaderm® side was significantly increased, resulting in complete wound healing in 12 days. Granulation thickness and vascularization were significantly increased during early wound healing. EGFP-ASCs could be retrieved by immunohistochemistry in the granulation tissue in early wound healing, and lining vascular structures in later stages.
[CONCLUSION] Glyaderm® is an effective carrier to deliver ASCs in full-thickness wounds. ASC-seeded Glyaderm® significantly enhances wound healing compared to standard Glyaderm®. The results of this study encourage clinical trials for treatment of full-thickness skin defects. Furthermore, xenogen-free isolation and autologous plasma-augmented culture expansion of ASCs, combined with the existing clinical experience with Glyaderm®, aid in simplifying the necessary procedures in a GMP-laboratory setting.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 시술 | liposuction
|
지방흡입 | dict | 1 | |
| 해부 | dermal matrix
|
scispacy | 1 | ||
| 해부 | adipose-derived stem cells
|
scispacy | 1 | ||
| 해부 | skin grafts
|
scispacy | 1 | ||
| 해부 | Dermal
|
scispacy | 1 | ||
| 해부 | skin
|
scispacy | 1 | ||
| 해부 | ASCs
→ Adipose-derived stem cells
|
scispacy | 1 | ||
| 해부 | Adipose tissue
|
scispacy | 1 | ||
| 해부 | abdominal
|
scispacy | 1 | ||
| 해부 | stromal cells
|
scispacy | 1 | ||
| 해부 | EGFP-transduced ASCs
|
scispacy | 1 | ||
| 해부 | granulation
|
scispacy | 1 | ||
| 해부 | cells
|
scispacy | 1 | ||
| 해부 | granulation tissue
|
scispacy | 1 | ||
| 합병증 | wound
|
scispacy | 1 | ||
| 합병증 | wounds
|
scispacy | 1 | ||
| 합병증 | dermal layer
|
scispacy | 1 | ||
| 합병증 | full-thickness wounds
|
scispacy | 1 | ||
| 재료 | acellular dermal matrix
|
무세포진피기질 | dict | 1 | |
| 약물 | [OBJECTIVE] Full-thickness
|
scispacy | 1 | ||
| 기타 | Human
|
scispacy | 1 | ||
| 기타 | murine
|
scispacy | 1 | ||
| 기타 | human ASCs
|
scispacy | 1 | ||
| 기타 | human acellular dermal matrix
|
scispacy | 1 | ||
| 기타 | murine immunodeficient wound
|
scispacy | 1 | ||
| 기타 | full-thickness dorsal wounds
|
scispacy | 1 | ||
| 기타 | immunodeficient murine
|
scispacy | 1 | ||
| 기타 | vascular
|
scispacy | 1 |
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