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10.3390/ijms18081614

http://scihub22266oqcxt.onion/10.3390/ijms18081614
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suck abstract from ncbi


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pmid28757565
      Int+J+Mol+Sci 2017 ; 18 (8 ): ä
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  • The Pharmaceutical Device Prisma(®) Skin Promotes in Vitro Angiogenesis through Endothelial to Mesenchymal Transition during Skin Wound Healing #MMPMID28757565
  • Belvedere R ; Bizzarro V ; Parente L ; Petrella F ; Petrella A
  • Int J Mol Sci 2017[Jul]; 18 (8 ): ä PMID28757565 show ga
  • Glycosaminoglycans are polysaccharides of the extracellular matrix supporting skin wound closure. Mesoglycan is a mixture of glycosaminoglycans such as chondroitin-, dermatan-, heparan-sulfate and heparin and is the main component of Prisma(®) Skin, a pharmaceutical device developed by Mediolanum Farmaceutici S.p.a. Here, we show the in vitro effects of this device in the new vessels formation by endothelial cells, since angiogenesis represents a key moment in wound healing. We found a strong increase of migration and invasion rates of these cells treated with mesoglycan and Prisma(®) Skin which mediate the activation of the pathway triggered by CD44 receptor. Furthermore, endothelial cells form longer capillary-like structures with a great number of branches, in the presence of the same treatments. Thus, the device, thanks to the mesoglycan, leads the cells to the Endothelial-to-Mesenchymal Transition, suggesting the switch to a fibroblast-like phenotype, as shown by immunofluorescence assays. Finally, we found that mesoglycan and Prisma(®) Skin inhibit inflammatory reactions such as nitric oxide secretion and NF-?B nuclear translocation in endothelial cells and Tumor Necrosis Factor-? production by macrophages. In conclusion, based on our data, we suggest that Prisma(®) Skin may be able to accelerate angiogenesis in skin wound healing, and regulate inflammation avoiding chronic, thus pathological, responses.
  • |Cell Movement [MESH]
  • |Cell Survival/drug effects [MESH]
  • |Endothelial Cells/cytology/drug effects [MESH]
  • |Epithelial-Mesenchymal Transition/*drug effects [MESH]
  • |Glycosaminoglycans/*pharmacology [MESH]
  • |Human Umbilical Vein Endothelial Cells [MESH]
  • |Humans [MESH]
  • |Hyaluronan Receptors/metabolism [MESH]
  • |In Vitro Techniques [MESH]
  • |Neovascularization, Physiologic/*drug effects [MESH]
  • |Pharmaceutical Preparations [MESH]
  • |Skin/*blood supply [MESH]


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