Topical Transplantation of Bone Marrow Mesenchymal Stem Cells Made Deeper Skin Wounds Regeneration

Current wound healing models generally employ full-thickness or irregular split wounds. Consequently, assessing the type of healing at varying wound depths and determining the deepest level at which wounds can regenerate has been a challenge. We describe a wound model that allows assessment of the healing process over a continuous gradient of wound depth, from epidermal to full-thickness dermal loss. Further, we investigate whether green fluorescent protein–labeled bone marrow mesenchymal stem cells (BM-MSCs/GFP) transplantation could regenerate deeper wounds that might otherwise lead to scar formation. A wound gradient was created on the back of 120 Sprague Dawley rats, which were randomized into the BM-MSCs/GFP and control group. These were further subdivided into 6 groups where terminal biopsies of the healing wounds were taken at days 1, 3, 5, 7, 14, and 21 post-operatively. At each observed time point, the experimental animals were anesthetized and photographed, and depending on the group, the animals euthanized and skin taken for rapid freezing, haemotoxylin and eosin staining, and vascular endothelial growth factor (VEGF) immunohistochemistry. We found the deepest layer to regenerate in the control group was at the level of the infundibulum apex, while in the BM-MSCs/GFP group this was deeper, at the opening site of sebaceous duct at hair follicle in which had the appearance of normal skin and less wound contraction than the control group (P value less than .05). The expression of VEGF in BM-MSCs/GFP group was higher than that in control group (P value less than .05). The number of vessels increased from 2.5 ± 0.2/phf of control group to 5.0 ± 0.3/phf of BM-MSCs/GFP (P value less than .05). The progressively deepening wound model we described can identify the type of wound repair at increasing depths. Further, topical transplantation of BM-MSCs/GFP significantly improved regeneration of deeper wounds from infundibulum apex (maximum depth of control group regeneration) to the opening site of sebaceous duct at hair follicle level.

[1]  R. Reis,et al.  Hydrogel-Based Strategies to Advance Therapies for Chronic Skin Wounds. , 2019, Annual review of biomedical engineering.

[2]  K. Matsumura,et al.  Effect of dual-drug-releasing micelle-hydrogel composite on wound healing in vivo in full-thickness excision wound rat model. , 2019, Journal of biomedical materials research. Part A.

[3]  J. Marchal,et al.  Therapeutic strategies for skin regeneration based on biomedical substitutes , 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

[4]  Jianping Wu,et al.  Evaluation of astaxanthin incorporated collagen film developed from the outer skin waste of squid Doryteuthis singhalensis for wound healing and tissue regenerative applications. , 2019, Materials science & engineering. C, Materials for biological applications.

[5]  Deshka S. Foster,et al.  Wound healing and fibrosis: current stem cell therapies , 2019, Transfusion.

[6]  Bhushan Mahadik,et al.  Current and Future Perspectives on Skin Tissue Engineering: Key Features of Biomedical Research, Translational Assessment, and Clinical Application , 2019, Advanced healthcare materials.

[7]  A. Abbaszadeh,et al.  Encapsulation of Satureja khuzistanica extract in alginate hydrogel accelerate wound healing in adult male rats , 2019, Inflammation and regeneration.

[8]  S. Bayat,et al.  Improvement in infected wound healing in type 1 diabetic rat by the synergistic effect of photobiomodulation therapy and conditioned medium , 2018, Journal of cellular biochemistry.

[9]  Qingsan Zhu,et al.  The Healing Effects of Conditioned Medium Derived from Mesenchymal Stem Cells on Radiation-Induced Skin Wounds in Rats , 2018, Cell transplantation.

[10]  C. Pizarro,et al.  Hyperbaric Oxygen Increases Stem Cell Proliferation, Angiogenesis and Wound-Healing Ability of WJ-MSCs in Diabetic Mice , 2018, Front. Physiol..

[11]  Rodney K. Chan,et al.  Advancements in Regenerative Strategies Through the Continuum of Burn Care , 2018, Front. Pharmacol..

[12]  S. Son,et al.  In vivo migration of mesenchymal stem cells to burn injury sites and their therapeutic effects in a living mouse model , 2018, Journal of controlled release : official journal of the Controlled Release Society.

[13]  P. Xue,et al.  Autophagy promotes MSC-mediated vascularization in cutaneous wound healing via regulation of VEGF secretion , 2018, Cell Death & Disease.

[14]  H. Alavi Majd,et al.  Effects of Acellular Amniotic Membrane Matrix and Bone Marrow-Derived Mesenchymal Stem Cells in Improving Random Skin Flap Survival in Rats , 2016, Iranian Red Crescent medical journal.

[15]  M. Maitz,et al.  Heparin desulfation modulates VEGF release and angiogenesis in diabetic wounds. , 2015, Journal of controlled release : official journal of the Controlled Release Society.

[16]  M. Plikus,et al.  Principles and mechanisms of regeneration in the mouse model for wound‐induced hair follicle neogenesis , 2015, Regeneration.

[17]  Austin Nuschke,et al.  Activity of mesenchymal stem cells in therapies for chronic skin wound healing , 2014, Organogenesis.

[18]  Y. Lyoo,et al.  The effects of topical mesenchymal stem cell transplantation in canine experimental cutaneous wounds , 2013, Veterinary dermatology.

[19]  H. Aithal,et al.  Evaluation of autologous bone marrow‐derived nucleated cells for healing of full‐thickness skin wounds in rabbits , 2010, International wound journal.

[20]  Murad Alam,et al.  Dermabrasion and microdermabrasion. , 2009, Facial plastic surgery : FPS.