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Bioprocessing strategies to enhance the challenging isolation of neuro-regenerative cells from olfactory mucosa.
Georgiou, Melanie; Reis, Joana Neves Dos; Wood, Rachael; Esteban, Patricia Perez; Roberton, Victoria; Mason, Chris; Li, Daqing; Li, Ying; Choi, David; Wall, Ivan.
Affiliation
  • Georgiou M; Department of Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, UK.
  • Reis JND; Cell and Gene Therapy Catapult, Guy's Hospital, Great Maze Pond, London, SE1 9RT, UK.
  • Wood R; Department of Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, UK.
  • Esteban PP; Department of Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, UK.
  • Roberton V; Aston Medical Research Institute and School of Life & Health Sciences, Aston University, Aston Triangle, Birmingham, B4 7ET, UK.
  • Mason C; Department of Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, UK.
  • Li D; Aston Medical Research Institute and School of Life & Health Sciences, Aston University, Aston Triangle, Birmingham, B4 7ET, UK.
  • Li Y; Department of Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, UK.
  • Choi D; Department of Biochemical Engineering, University College London, Torrington Place, London, WC1E 7JE, UK.
  • Wall I; Spinal Repair Unit, Department of Brain, Repair and Rehabilitation, Institute of Neurology, University College London, Queen Square, London, WC1N 3BG, UK.
Sci Rep ; 8(1): 14440, 2018 09 27.
Article in En | MEDLINE | ID: mdl-30262897
Olfactory ensheathing cells (OECs) are a promising potential cell therapy to aid regeneration. However, there are significant challenges in isolating and characterizing them. In the current study, we have explored methods to enhance the recovery of cells expressing OEC marker p75NTR from rat mucosa. With the addition of a 24-hour differential adhesion step, the expression of p75NTR was significantly increased to 73 ± 5% and 46 ± 18% on PDL and laminin matrices respectively. Additionally, the introduction of neurotrophic factor NT-3 and the decrease in serum concentration to 2% FBS resulted in enrichment of OECs, with p75NTR at nearly 100% (100 ± 0% and 98 ± 2% on PDL and laminin respectively), and candidate fibroblast marker Thy1.1 decreased to zero. Culturing OECs at physiologically relevant oxygen tension (2-8%) had a negative impact on p75NTR expression and overall cell survival. Regarding cell potency, co-culture of OECs with NG108-15 neurons resulted in more neuronal growth and potential migration at atmospheric oxygen. Moreover, OECs behaved similarly to a Schwann cell line positive control. In conclusion, this work identified key bioprocessing fundamentals that will underpin future development of OEC-based cell therapies for potential use in spinal cord injury repair. However, there is still much work to do to create optimized isolation methods.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Separation / Olfactory Mucosa / Cell Culture Techniques / Neurons Type of study: Prognostic_studies Limits: Animals Language: En Journal: Sci Rep Year: 2018 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Separation / Olfactory Mucosa / Cell Culture Techniques / Neurons Type of study: Prognostic_studies Limits: Animals Language: En Journal: Sci Rep Year: 2018 Document type: Article Country of publication: United kingdom