Generation and characterization of neurospheres from canine adipose tissue-derived stromal cells

Cell Reprogram. 2010 Aug;12(4):417-25. doi: 10.1089/cell.2009.0093.

Abstract

Adipose tissue-derived stromal cells (ADSCs) have been identified as a powerful stem cell source for cellular transplantation therapy. The dog is increasingly used as a model of human neurological disease; however, few studies have reported induction of canine ADSCs to neural lineages. We characterized canine ADSCs and investigated whether they could be induced to differentiate into neural lineages. Subcutaneous adipose tissue collected from the dorsal epaxial region of adult dogs aged from 1 to 6 years was cultured to produce ADSCs that were then induced to neural lineages. RT-PCR, flow cytometry, and immunocytochemistry were performed to characterize these cell populations. Morphologically fibroblast-like ADSCs were isolated and had similar characteristics to mesenchymal stem cells. Under neurogenic conditions containing basic fibroblast growth factor and epidermal growth factor, ADSCs formed spherical cellular aggregates that resembled neurospheres. RT-PCR confirmed expression of Sox2 and CD90 by these aggregates. Expression of neural stem/progenitor markers (Nestin, Sox2, Vimentin) and neural lineage markers (A2B5, GFAP, Tuj1) was shown on immunocytochemistry. After differentiation, 60% of the cells were Tuj1 positive. In conclusion, we isolated and generated neural progenitor cells from canine ADSCs. ADSCs have potential for future autologous cell transplantation therapy for neurological disorders.

MeSH terms

  • Adipose Tissue / metabolism*
  • Animals
  • Biomarkers / metabolism
  • Blotting, Western
  • Bone and Bones / cytology
  • Bone and Bones / metabolism
  • Cell Differentiation*
  • Cell Lineage
  • Cells, Cultured
  • Dogs
  • Flow Cytometry
  • Neurons / metabolism*
  • Osteogenesis
  • Phenotype
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cells / cytology*
  • Stromal Cells / metabolism*

Substances

  • Biomarkers
  • RNA, Messenger