| dc.creator | Di Somma M., Schaafsma W., Grillo E., Vliora M., Dakou E., Corsini M., Ravelli C., Ronca R., Sakellariou P., Vanparijs J., Castro B., Mitola S. | en |
| dc.date.accessioned | 2023-01-31T07:54:23Z | |
| dc.date.available | 2023-01-31T07:54:23Z | |
| dc.date.issued | 2019 | |
| dc.identifier | 10.3390/cells8111457 | |
| dc.identifier.issn | 20734409 | |
| dc.identifier.uri | http://hdl.handle.net/11615/73250 | |
| dc.description.abstract | In the treatment of obesity and its related disorders, one of the measures adopted is weight reduction by controlling nutrition and increasing physical activity. A valid alternative to restore the physiological function of the human body could be the increase of energy consumption by inducing the browning of adipose tissue. To this purpose, we tested the ability of Histogel, a natural mixture of glycosaminoglycans isolated from animal Wharton jelly, to sustain the differentiation of adipose derived mesenchymal cells (ADSCs) into brown-like cells expressing UCP-1. Differentiated cells show a higher energy metabolism compared to undifferentiated mesenchymal cells. Furthermore, Histogel acts as a pro-angiogenic matrix, induces endothelial cell proliferation and sprouting in a three-dimensional gel in vitro, and stimulates neovascularization when applied in vivo on top of the chicken embryo chorioallantoic membrane or injected subcutaneously in mice. In addition to the pro-angiogenic activity of Histogel, also the ADSC derived beige cells contribute to activating endothelial cells. These data led us to propose Histogel as a promising scaffold for the modulation of the thermogenic behavior of adipose tissue. Indeed, Histogel simultaneously supports the acquisition of brown tissue markers and activates the vasculature process necessary for the correct function of the thermogenic tissue. Thus, Histogel represents a valid candidate for the development of bioscaffolds to increase the amount of brown adipose tissue in patients with metabolic disorders. © 2019 by the authors. Licensee MDPI, Basel, Switzerland. | en |
| dc.language.iso | en | en |
| dc.source | Cells | en |
| dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85088609830&doi=10.3390%2fcells8111457&partnerID=40&md5=d5cc16d4077a029b301854c0ff8c50c0 | |
| dc.subject | adiponectin receptor 1 | en |
| dc.subject | fibroblast growth factor | en |
| dc.subject | glycosaminoglycan | en |
| dc.subject | hyaluronic acid | en |
| dc.subject | messenger RNA | en |
| dc.subject | peroxisome proliferator activated receptor gamma | en |
| dc.subject | placental growth factor | en |
| dc.subject | platelet derived growth factor | en |
| dc.subject | pyruvate dehydrogenase kinase 4 | en |
| dc.subject | uncoupling protein 1 | en |
| dc.subject | vasculotropin A | en |
| dc.subject | glycosaminoglycan | en |
| dc.subject | agar gel electrophoresis | en |
| dc.subject | angiogenesis | en |
| dc.subject | angiogenesis assay | en |
| dc.subject | animal experiment | en |
| dc.subject | antiangiogenic activity | en |
| dc.subject | Article | en |
| dc.subject | basal metabolic rate | en |
| dc.subject | beige adipose tissue | en |
| dc.subject | cell differentiation | en |
| dc.subject | cell proliferation | en |
| dc.subject | cell viability assay | en |
| dc.subject | chick embryo | en |
| dc.subject | chorioallantoic membrane assay | en |
| dc.subject | controlled study | en |
| dc.subject | embryo | en |
| dc.subject | energy expenditure | en |
| dc.subject | energy metabolism | en |
| dc.subject | gel | en |
| dc.subject | histogel | en |
| dc.subject | human | en |
| dc.subject | human cell | en |
| dc.subject | immunofluorescence test | en |
| dc.subject | infant | en |
| dc.subject | inflammation | en |
| dc.subject | mesenchymal stem cell | en |
| dc.subject | metabolic activity assay | en |
| dc.subject | metabolic disorder | en |
| dc.subject | mouse | en |
| dc.subject | MTT assay | en |
| dc.subject | nonhuman | en |
| dc.subject | protein expression | en |
| dc.subject | real time polymerase chain reaction | en |
| dc.subject | sprouting angiogenesis | en |
| dc.subject | stem cell culture | en |
| dc.subject | stereomicroscopy | en |
| dc.subject | vascularization | en |
| dc.subject | angiogenesis | en |
| dc.subject | animal | en |
| dc.subject | beige adipose tissue | en |
| dc.subject | cell culture | en |
| dc.subject | chemistry | en |
| dc.subject | cytology | en |
| dc.subject | drug effect | en |
| dc.subject | metabolism | en |
| dc.subject | thermogenesis | en |
| dc.subject | tissue scaffold | en |
| dc.subject | vascularization | en |
| dc.subject | Wharton jelly | en |
| dc.subject | Adipose Tissue, Beige | en |
| dc.subject | Animals | en |
| dc.subject | Cell Differentiation | en |
| dc.subject | Cell Proliferation | en |
| dc.subject | Cells, Cultured | en |
| dc.subject | Chick Embryo | en |
| dc.subject | Energy Metabolism | en |
| dc.subject | Glycosaminoglycans | en |
| dc.subject | Humans | en |
| dc.subject | Mesenchymal Stem Cells | en |
| dc.subject | Mice | en |
| dc.subject | Neovascularization, Physiologic | en |
| dc.subject | Thermogenesis | en |
| dc.subject | Tissue Scaffolds | en |
| dc.subject | Wharton Jelly | en |
| dc.subject | MDPI | en |
| dc.title | Natural histogel-based bio-scaffolds for sustaining angiogenesis in beige adipose tissue | en |
| dc.type | journalArticle | en |