Comparative study of regenerative effects of mesenchymal stem cells derived from placental amnion, chorion and umbilical cord on dermal wounds. (May 2018)

• Record Type: Journal Article
• Authors: Ertl, Juliane; Pichlsberger, Melanie; Tuca, Alexandru-Cristian; Wurzer, Paul; Fuchs, Jakob; Geyer, Stefan H.; Maurer-Gesek, Barbara; Weninger, Wolfgang J.; Pfeiffer, Dagmar; Bubalo, Vladimir; Parvizi, Daryousch; Kamolz, Lars-Peter; Lang, Ingrid
• Is Part Of: Placenta. Volume 65(2018)
• Page Start: 37
• Page End: 46
• Publication Date: 2018-05
• Subjects: Human placenta -- Amnion -- Umbilical cord -- Blood vessels -- Mesenchymal stem cells -- Wound healing -- Angiogenesis -- Mouse model; Placenta -- Periodicals; Reproduction -- Periodicals; Placenta -- Periodicals; Placenta -- Périodiques; Reproduction -- Périodiques; 612.63
• DOI: 10.1016/j.placenta.2018.04.004
• Languages: English
• ISSNs: 0143-4004

Abstract

Abstract: Objective: Mesenchymal stem/stromal cells derived from human term placentas (PMSCs) are novel therapeutic agents and more topical than ever. Here we evaluated the effects of three types of PMSCs on wound healing in an in vivo mouse model: Amnion-derived MSCs (AMSCs), blood vessel-derived MSCs (BV-MSCs) from the chorionic plate and Wharton's jelly-derived MSCs (WJ-MSCs) from the umbilical cord. Methods: We topically applied PMSCs onto skin wounds in mice using the dermal substitute Matriderm ® as carrier and evaluated wound healing parameters. In addition, we investigated the effects of all PMSC types under co-application with placental endothelial cells (PLECs). After 8 days, we compared the percent of wound closure and the angiogenic potential between all groups. Results: AMSCs, BV-MSCs and WJ-MSCs significantly induced a faster healing and a higher number of blood vessels in the wound when compared to controls (Matriderm ® -alone). PLECs did not further improve the advantageous effects of PMSC-treatment. Quantitative data and 3D analysis by high resolution episcopic microscopy confirmed a lower density of vessels in Matriderm ® /PMSCs/PLECs co-application compared to Matriderm ® /PMSCs treatment. Conclusion: Results indicate that all three PMSC types exert similar beneficial effects on wound closure and neovascularization in our mouse model. Practice: Using Matriderm ® as carrier for PMSCs propagates rapid cell migration towards the wound area that allows a fast and clinically practicable method for stem cell application. Implications: These promising effects warrant further investigation in clinical trials. Highlights: 3 types of placental mesenchymal stem cells (PMSCs) were tested in a mouse model. PMSCs from amnion, chorionic blood vessels and umbilical cord promote wound healing. Matriderm as carrier for PMSCs propagates rapid cell migration towards the wound. PMSCs co-application with endothelial cells does not further improve wound healing.