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A Guide to Extract Spinal Cord for Translational Stem Cell Biology Research: Comparative Analysis of Adult Human, Porcine, and Rodent Spinal Cord Stem Cells.
Galuta, Ahmad; Sandarage, Ryan; Ghinda, Diana; Auriat, Angela M; Chen, Suzan; Kwan, Jason C S; Tsai, Eve C.
Afiliação
  • Galuta A; Department of Neurosciences, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
  • Sandarage R; Neuroscience Program, Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, ON, Canada.
  • Ghinda D; Department of Neurosciences, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
  • Auriat AM; Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
  • Chen S; Neuroscience Program, Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, ON, Canada.
  • Kwan JCS; Division of Neurosurgery, Department of Surgery, The Ottawa Hospital, Ottawa, ON, Canada.
  • Tsai EC; Neuroscience Program, Ottawa Hospital Research Institute, The Ottawa Hospital, Ottawa, ON, Canada.
Front Neurosci ; 14: 607, 2020.
Article em En | MEDLINE | ID: mdl-32625055
ABSTRACT
Improving the clinical translation of animal-based neural stem/progenitor cell (NSPC) therapies to humans requires an understanding of intrinsic human and animal cell characteristics. We report a novel in vitro method to assess spinal cord NSPCs from a small (rodent) and large (porcine) animal model in comparison to human NSPCs. To extract live adult human, porcine, and rodent spinal cord tissue, we illustrate a strategy using an anterior or posterior approach that was simulated in a porcine model. The initial expansion of primary NSPCs is carried out using the neurosphere assay followed by a pharmacological treatment phase during which NSPCs derived from humans, porcines, and rodents are assessed in parallel using the same defined parameters. Using this model, NSPCs from all species demonstrated multi-lineage differentiation and self-renewal. Importantly, these methods provide conditions to enable the direct comparison of species-dependent cell behavior in response to specific exogenous signals.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Neurosci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Neurosci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá