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Viability of mesenchymal stem cells during electrospinning
Zanatta, G; Steffens, D; Braghirolli, D. I; Fernandes, R. A; Netto, C. A; Pranke, P.
  • Zanatta, G; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
  • Steffens, D; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
  • Braghirolli, D. I; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
  • Fernandes, R. A; Grupo Hospitalar Conceição. Hospital Nossa Senhora da Conceição. Porto Alegre. BR
  • Netto, C. A; Universidade Federal do Rio Grande do Sul. Departamento de Bioquímica. Laboratório de Isquemia Cerebral. Porto Alegre. BR
  • Pranke, P; Universidade Federal do Rio Grande do Sul. Faculdade de Farmácia. Laboratório de Hematologia e Células-tronco. Porto Alegre. BR
Braz. j. med. biol. res ; 45(2): 125-130, Feb. 2012. ilus
Article in English | LILACS | ID: lil-614573
ABSTRACT
Tissue engineering is a technique by which a live tissue can be re-constructed and one of its main goals is to associate cells with biomaterials. Electrospinning is a technique that facilitates the production of nanofibers and is commonly used to develop fibrous scaffolds to be used in tissue engineering. In the present study, a different approach for cell incorporation into fibrous scaffolds was tested. Mesenchymal stem cells were extracted from the wall of the umbilical cord and mononuclear cells from umbilical cord blood. Cells were re-suspended in a 10 percent polyvinyl alcohol solution and subjected to electrospinning for 30 min under a voltage of 21 kV. Cell viability was assessed before and after the procedure by exclusion of dead cells using trypan blue staining. Fiber diameter was observed by scanning electron microscopy and the presence of cells within the scaffolds was analyzed by confocal laser scanning microscopy. After electrospinning, the viability of mesenchymal stem cells was reduced from 88 to 19.6 percent and the viability of mononuclear cells from 99 to 8.38 percent. The loss of viability was possibly due to the high viscosity of the polymer solution, which reduced the access to nutrients associated with electric and mechanical stress during electrospinning. These results suggest that the incorporation of cells during fiber formation by electrospinning is a viable process that needs more investigation in order to find ways to protect cells from damage.
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Full text: Available Index: LILACS (Americas) Main subject: Leukocytes, Mononuclear / Electrochemistry / Mesenchymal Stem Cells Limits: Humans / Infant, Newborn Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2012 Type: Article Affiliation country: Brazil Institution/Affiliation country: Grupo Hospitalar Conceição/BR / Universidade Federal do Rio Grande do Sul/BR

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Full text: Available Index: LILACS (Americas) Main subject: Leukocytes, Mononuclear / Electrochemistry / Mesenchymal Stem Cells Limits: Humans / Infant, Newborn Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2012 Type: Article Affiliation country: Brazil Institution/Affiliation country: Grupo Hospitalar Conceição/BR / Universidade Federal do Rio Grande do Sul/BR