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1.
Cell Biochem Funct ; 29(4): 311-33, 2011 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-21491468

RESUMEN

The particular combination of polydeoxyribonucleotides, l-carnitine, calcium ions, proteolytic enzyme and other ingredients acts in a synergetic way in the regeneration of skin and connective tissues. This new formulation of active principles was tested in vitro as a cell and tissue culture medium and in vivo for various preparations in support of tissue regeneration. In vitro, the new blend allowed the maintenance of skin biopsies for more than 1 year in eutrophic conditions. Immunocytochemical analyses of fibroblasts isolated from these biopsies confirmed a significant increase of the epidermal and connective wound-healing markers such as collagen type I, collagen type IV, cytokeratin 1 (CK1), CK5, CK10 and CK14 versus controls. To examine the effects of the new compound in vivo, we studied impaired wound healing in genetically diabetic db/db mice. At day 18, diabetic mice treated with the new composition showed 100% closure of wounds and faster healing than mice treated with the other solutions. This complex of vital continuity factors or life-keeping factors could be used as a tissue-preserving solution or a cosmetic/drug/medical device to accelerate wound healing in the treatment of patients with deficient wound repair to promote the regeneration of cutaneous and connective tissues (injuries-wound, dermatitis) and prevent the recurrent relapses.


Asunto(s)
Química Farmacéutica , Tejido Conectivo/crecimiento & desarrollo , Medios de Cultivo/farmacología , Piel/crecimiento & desarrollo , Cicatrización de Heridas , Administración Tópica , Animales , Biopsia , Peso Corporal , Supervivencia Celular , Células Cultivadas , Colágeno Tipo I/metabolismo , Colágeno Tipo II/metabolismo , Tejido Conectivo/efectos de los fármacos , Medios de Cultivo/química , Diabetes Mellitus/patología , Fibroblastos/efectos de los fármacos , Fibroblastos/fisiología , Humanos , Inmunohistoquímica , Queratinas/metabolismo , Masculino , Ratones , Polidesoxirribonucleótidos/farmacología , Piel/efectos de los fármacos , Coloración y Etiquetado/métodos
2.
Exp Cell Res ; 316(11): 1804-15, 2010 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-20156437

RESUMEN

Cell-based therapy could be a valid option to treat myocardial infarct (MI). Adipose-derived stromal cells (ADStCs) have demonstrated tissue regenerative potential including cardiomyogenesis. Omentum is an extremely rich source of visceral fat and its accumulation seems to correlate with cardiovascular diseases. We investigated the capacity of human fat Omentum-derived StCs (FOStCs) to affect heart function upon acute infarct in pigs induced by permanent ligation of the anterior interventricular artery (IVA). We demonstrated for the first time that the local injection of 50x10(6) of FOStCs ameliorates the functional parameters of post-infarct heart. Most importantly, histology of FOStCs treated hearts demonstrated a substantial improvement of cardiomyogenesis. In culture, FOStCs produced an impressive number and amount of angiogenic factors and cytokines. Moreover, the conditioned medium of FOStCs (FOStCs-CM) stimulates in vitro cardiac endothelial cells (ECs) proliferation and vascular morphogenesis and inhibits monocytes, EC activation and cardiomyocyte apoptosis. Since FOStCs in vivo did not trans-differentiate into cardiomyocyte-like cells, we conclude that FOStCs efficacy was presumably mediated by a potent paracrine mechanism involving molecules that concomitantly improved angiogenesis, reduced inflammation and prevented cardiomyocytes death. Our results highlight for the first time the important role that human FOStCs may have in cardiac regeneration.


Asunto(s)
Infarto del Miocardio/terapia , Epiplón/citología , Regeneración/fisiología , Células del Estroma/fisiología , Células del Estroma/trasplante , Animales , Apoptosis , Diferenciación Celular , Proliferación Celular , Células Cultivadas , Células Endoteliales/patología , Células Endoteliales/fisiología , Femenino , Corazón/fisiología , Humanos , Técnicas In Vitro , Ratones , Infarto del Miocardio/patología , Infarto del Miocardio/fisiopatología , Miocitos Cardíacos/patología , Miocitos Cardíacos/fisiología , Neovascularización Fisiológica , Comunicación Paracrina , Células del Estroma/citología , Porcinos
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