Seizure: European Journal of Epilepsy
Volume 19, Issue 7 , Pages 390-396 , September 2010

Astrocytes derived from fetal neural progenitor cells as a novel source for therapeutic adenosine delivery

  • Annelies Van Dycke

      Affiliations

    • Laboratory for Clinical and Experimental Neurophysiology, Department of Neurology, Ghent University Hospital, 1K12, 185 De Pintelaan, 9000 Ghent, Belgium
    • Corresponding Author InformationCorresponding author. Tel.: +32 9 332 6946; fax: +32 9 332 4971.
  • ,
  • Robrecht Raedt

      Affiliations

    • Laboratory for Clinical and Experimental Neurophysiology, Department of Neurology, Ghent University Hospital, 1K12, 185 De Pintelaan, 9000 Ghent, Belgium
  • ,
  • Alain Verstraete

      Affiliations

    • Laboratory of Clinical Biology, Ghent University Hospital, Ghent, Belgium
  • ,
  • Panos Theofilas

      Affiliations

    • Robert Stone Dow Neurobiology Laboratories, Legacy Research, Portland, OR, USA
  • ,
  • Wytse Wadman

      Affiliations

    • Laboratory for Clinical and Experimental Neurophysiology, Department of Neurology, Ghent University Hospital, 1K12, 185 De Pintelaan, 9000 Ghent, Belgium
    • Swammerdam Institute of Life Sciences, Department of Neurobiology, University of Amsterdam, Amsterdam, The Netherlands
  • ,
  • Kristl Vonck

      Affiliations

    • Laboratory for Clinical and Experimental Neurophysiology, Department of Neurology, Ghent University Hospital, 1K12, 185 De Pintelaan, 9000 Ghent, Belgium
  • ,
  • Detlev Boison

      Affiliations

    • Robert Stone Dow Neurobiology Laboratories, Legacy Research, Portland, OR, USA
  • ,
  • Paul Boon

      Affiliations

    • Laboratory for Clinical and Experimental Neurophysiology, Department of Neurology, Ghent University Hospital, 1K12, 185 De Pintelaan, 9000 Ghent, Belgium

Received 31 March 2010 ,Revised 8 May 2010 ,Accepted 21 May 2010.

  • Image Result

    PCR and Western Blot. (A) PCR: results of isolated cells from Adk+/−×Adk+/− matings. Based on these results, an Adk−/− clone needed for the experiment could be detected. The genomic DNA was amplified

    PCR and Western Blot. (A) PCR: results of isolated cells from Adk+/−×Adk+/− matings. Based on these results, an Adk−/− clone needed for the experiment could be detected. The genomic DNA was amplified using the three allele-specific primers o107, o108 and o109. DNA from Adk+/− cells gives a combination of the wild-type specific 640bp band (primers o107/o108) and the knockout-specific 840bp band (primers o107/o109), while DNA from Adk−/− cells gives rise to only a 840bp band (primers o107/o109), demonstrating the bi-allelic genetic disruption of the Adk locus. (B) Western Blot: above the GAPDH immune reactivity for protein control is shown (38kDa). Beneath ADK immune reactivity is shown (44–46kDa). A clear reactivity is found in wild-type cells, whereas no reactivity is found in non-differentiated and differentiated Adk−/− cells (CO=control wild-type; KO 1d=Adk−/− after 24h; KO 1w=Adk−/− after 1 week).

  • Image Result
    Expression of neural stem cell markers. Left: Immunostaining with nestin (red) and GFAP (green) in Adk−/− cells (A) and wild-type cells (C). Scale bar=100μm. Right: Immunostaining with Sox2 (red) in A

    Expression of neural stem cell markers. Left: Immunostaining with nestin (red) and GFAP (green) in Adk−/− cells (A) and wild-type cells (C). Scale bar=100μm. Right: Immunostaining with Sox2 (red) in Adk−/− cells (B) and wild-type cells (D). Scale bar=50μm. Nuclei are stained with DAPI (blue).

  • Image Result
    Glial and neural differentiation of neural progenitor cells in vitro. Left: Immunostaining with GFAP (red) in Adk−/− cells (A) and wild-type cells (C). Right: Immunostaining with tau (red) in Adk−/− c

    Glial and neural differentiation of neural progenitor cells in vitro. Left: Immunostaining with GFAP (red) in Adk−/− cells (A) and wild-type cells (C). Right: Immunostaining with tau (red) in Adk−/− cells (B) and wild-type cells (D). Nuclei are stained with DAPI (blue). Scale bar=100μm.

  • Image Result
    Adenosine releases from Adk−/− cells (blue) and corresponding wild-type cells (red) in 24h. (A) Adenosine released from 100,000 non-differentiated cells: adenosine release from Adk−/− cells is signifi

    Adenosine releases from Adk−/− cells (blue) and corresponding wild-type cells (red) in 24h. (A) Adenosine released from 100,000 non-differentiated cells: adenosine release from Adk−/− cells is significantly higher compared to wild-type cells. (B) Adenosine released from 100,000 differentiated cells: adenosine release from Adk−/− cells is significantly higher compared to wild-type cells. Standard errors are marked with black bars. Significance is marked with an asterisk (*): p<0.05.

PII: S1059-1311(10)00114-7

doi: 10.1016/j.seizure.2010.05.010

Seizure: European Journal of Epilepsy
Volume 19, Issue 7 , Pages 390-396 , September 2010