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      Mesenchymal stem cells derivatives as a novel and potential therapeutic approach to treat diabetic foot ulcers

      research-article
      1 , 1 , 1 , 2 , 3 , 3 , 2 , 2
      Endocrinology, Diabetes & Metabolism Case Reports
      Bioscientifica Ltd
      Geriatric, Male, Hispanic or Latino - Central American or South American, Colombia, Skin, Diabetes, Insulin, Diabetic foot syndrome, Diabetic foot ulceration, Hyperglycaemia, Wound size*, Wound closure*, Wound area*, Wound volume*, Wound depth*, Ganulation tissue*, Cytokines, Growth factors*, Mesenchymal stem cell transplantation*, Mesenchymal stem cell derivatives transplantation*, Losartan, Levothyroxine, Atorvastatin, Acetylsalysilic acid*, Metformin, Insulin glargine, Insulin glulisine, Carvedilol, Diclofenac*, Acetaminophen*, Saline, Dermatology, Novel treatment, July, 2020

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          Abstract

          Summary

          Diabetic foot ulcer morbidity and mortality are dramatically increasing worldwide, reinforcing the urgency to propose more effective interventions to treat such a devastating condition. Previously, using a diabetic mouse model, we demonstrated that administration of bone marrow mesenchymal stem cells derivatives is more effective than the use of bone marrow mesenchymal stem cells alone. Here, we used the aforementioned treatments on three patients with grade 2 diabetic foot ulcers and assessed their beneficial effects, relative to the conventional approach. In the present study, two doses of cell derivatives, one dose of mesenchymal stem cells or one dose of vehicle (saline solution with 5% of human albumin), were intradermally injected around wounds. Wound healing process and changes on re-epithelialization were macroscopically evaluated until complete closure of the ulcers. All ulcers were simultaneously treated with conventional treatment (PolyMen® dressing). Patients treated with either cell derivatives or mesenchymal stem cells achieved higher percentages of wound closure in shorter times, relative to the patient treated with the conventional treatment. The cell derivative and mesenchymal stem cells approaches resulted in complete wound closure and enhanced skin regeneration at some point between days 35 and 42, although no differences between these two treatments were observed. Moreover, wounds treated with the conventional treatment healed after 161 days. Intradermal administration of cell derivatives improved wound healing to a similar extent as mesenchymal stem cells. Thus, our results suggest that mesenchymal stem cell derivatives may serve as a novel and potential therapeutic approach to treat diabetic foot ulcers.

          Learning points:
          • In diabetic mouse models, the administration of mesenchymal stem cells derivatives have been demonstrated to be more effective than the use of marrow mesenchymal stem cells alone.

          • Mesenchymal stem cells have been explored as an attractive therapeutic option to treat non-healing ulcers.

          • Mesenchymal stem cells derivatives accelerate the re-epithelialization on diabetic foot ulcers.

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          Most cited references7

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          Mesenchymal Stem Cells Are Recruited into Wounded Skin and Contribute to Wound Repair by Transdifferentiation into Multiple Skin Cell Type

          Mesenchymal stem cells (MSCs) can differentiate not only into mesenchymal lineage cells but also into various other cell lineages. As MSCs can easily be isolated from bone marrow, they can be used in various tissue engineering strategies. In this study, we assessed whether MSCs can differentiate into multiple skin cell types including keratinocytes and contribute to wound repair. First, we found keratin 14-positive cells, presumed to be keratinocytes that transdifferentiated from MSCs in vitro. Next, we assessed whether MSCs can transdifferentiate into multiple skin cell types in vivo. At sites of mouse wounds that had been i.v. injected with MSCs derived from GFP transgenic mice, we detected GFP-positive cells associated with specific markers for keratinocytes, endothelial cells, and pericytes. Because MSCs are predominantly located in bone marrow, we investigated the main MSC recruitment mechanism. MSCs expressed several chemokine receptors; especially CCR7, which is a receptor of SLC/CCL21, that enhanced MSC migration. Finally, MSC-injected mice underwent rapid wound repaired. Furthermore, intradermal injection of SLC/CCL21 increased the migration of MSCs, which resulted in an even greater acceleration of wound repair. Taken together, we have demonstrated that MSCs contribute to wound repair via processes involving MSCs differentiation various cell components of the skin.
            • Record: found
            • Abstract: not found
            • Article: not found

            Cell secretome based drug substances in regenerative medicine: when regulatory affairs meet basic science.

              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              The role of bone marrow mesenchymal stromal cell derivatives in skin wound healing in diabetic mice

              Mesenchymal stromal cells (MSCs) have shown to be a promising tool in cell therapies to treat different conditions. Several pre-clinical and clinical studies have proved that the transplantation of MSCs improves wound healing. Here, we compare the beneficial effects of mouse bone marrow-derived allogeneic MSCs (allo-mBM-MSCs) and their acelullar derivatives (allo-acd-mMSCs) on skin wound healing in Non-Obese Diabetic (NOD) mice. One dose of allo-mBM-MSCs (1×106 cells) or one dose of allo-acd-mMSCs (1X) were intradermally injected around wounds in 8–10 week old female NOD mice. Wound healing was evaluated macroscopically (wound closure) every two days, and microscopically (reepithelialization, dermoepidermal junction, skin appendage regeneration, leukocyte infiltration, vascularization, granulation tissue formation, and density of collagen fibers in the dermis) after 16 days of MSC injection. In addition, we measured growth factors and specific proteins that were present in the allo-acd-mMSCs. Results showed significant differences in the wound healing kinetics of lesions that received allo-acd-mMSCs compared to lesions that received vehicle or allo-mBM-MSCs. In particular, mice treated with allo-acd-mMSCs reached significantly higher percentages of wound closure at day 4, 6 and 8, relative to the allo-mBM-MSCs and vehicle groups (p < 0.05), while wound closure percentages could not be statistically distinguished between the allo-mBM-MSCs and vehicle groups. Also, allo-acd-mMSCs had a greater influence in the skin would healing process. Specifically, they caused a less pronounced inflammatory severe response (p < 0.0001), more granulation tissue formation at an advanced stage (p < 0.0001), and higher density of collagen fibers (p < 0.05) compared to the other groups. Nevertheless, at day 16, both allo-mBM-MSCs and allo-acd-mMSCs revealed a higher effect on the recovery of the quality skin (continuous epidermis; regular dermoepidermal junction and skin appendages) relative to untreated lesions (p < 0.0001), but not between them. On the other hand, ELISA analyses indicated that the allo-acd-mMSCs contained growth factors and proteins relevant to wound healing such as IGF-1, KGF, HGF, VEGF, ANG-2, MMP-1, CoL-1 and PGE2. Compared to allo-acd-mMSCs, the administration of allo-mBM-MSCs is insufficient for wound healing in diabetic mice and delays the therapeutic effect, which maybe explained by the fact that trophic factors secreted by MSCs are critical for skin regeneration, and not the cells per se, suggesting that MSCs may require some time to secrete these factors after their administration.

                Author and article information

                Journal
                Endocrinol Diabetes Metab Case Rep
                Endocrinol Diabetes Metab Case Rep
                EDM
                Endocrinology, Diabetes & Metabolism Case Reports
                Bioscientifica Ltd (Bristol )
                2052-0573
                05 July 2020
                2020
                : 2020
                : 19-0164
                Affiliations
                [1 ]Facultad de Ciencias de la Salud , Universidad Autónoma de Bucaramanga – UNAB, Bucaramanga, Colombia
                [2 ]Banco Multitejidos y Centro de Terapias Avanzadas , Fundación Oftalmológica de Santander, Clínica Carlos Ardila Lulle – FOSCAL, Floridablanca, Colombia
                [3 ]Fundación Oftalmológica de Santander , Clínica Carlos Ardila Lulle – FOSCAL, Floridablanca, Colombia
                Author notes
                Correspondence should be addressed to M L Arango-Rodríguez; Email: martha.arango@ 123456foscal.com.co
                Article
                EDM190164
                10.1530/EDM-19-0164
                7354732
                32698128
                1da4af8b-fd0a-4172-aa5c-5de0d6b6f403
                © 2020 The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License..

                History
                : 02 April 2020
                : 26 May 2020
                Categories
                Geriatric
                Male
                Hispanic or Latino - Central American or South American
                Colombia
                Skin
                Diabetes
                Insulin
                Diabetic Foot Syndrome
                Diabetic Foot Ulceration
                Hyperglycaemia
                Wound Size*
                Wound Closure*
                Wound Area*
                Wound Volume*
                Wound Depth*
                Ganulation Tissue*
                Cytokines
                Growth Factors*
                Mesenchymal Stem Cell Transplantation*
                Mesenchymal Stem Cell Derivatives Transplantation*
                Losartan
                Levothyroxine
                Atorvastatin
                Acetylsalysilic Acid*
                Metformin
                Insulin Glargine
                Insulin Glulisine
                Carvedilol
                Diclofenac*
                Acetaminophen*
                Saline
                Dermatology
                Novel Treatment
                Novel Treatment

                geriatric,male,hispanic or latino - central american or south american,colombia,skin,diabetes,insulin,diabetic foot syndrome,diabetic foot ulceration,hyperglycaemia,wound size*,wound closure*,wound area*,wound volume*,wound depth*,ganulation tissue*,cytokines,growth factors*,mesenchymal stem cell transplantation*,mesenchymal stem cell derivatives transplantation*,losartan,levothyroxine,atorvastatin,acetylsalysilic acid*,metformin,insulin glargine,insulin glulisine,carvedilol,diclofenac*,acetaminophen*,saline,dermatology,novel treatment,july,2020

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