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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
-
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 640
bp band (primers o107/o108) and the knockout-specific 840
bp band (primers o107/o109), while DNA from Adk−/− cells gives rise to only a 840
bp 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 (38
kDa). Beneath ADK immune reactivity is shown (44–46
kDa). 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 24
h; KO 1w
=
Adk−/− after 1 week). -
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 AExpression of neural stem cell markers. Left: Immunostaining with nestin (red) and GFAP (green) in Adk−/− cells (A) and wild-type cells (C). Scale bar
=
100
μm. Right: Immunostaining with Sox2 (red) in Adk−/− cells (B) and wild-type cells (D). Scale bar
=
50
μm. Nuclei are stained with DAPI (blue). -
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−/− cGlial 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
=
100
μm. -
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 signifiAdenosine releases from Adk−/− cells (blue) and corresponding wild-type cells (red) in 24
h. (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
© 2010 British Epilepsy Association. Published by Elsevier Inc. All rights reserved.
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Seizure: European Journal of Epilepsy
Volume 19, Issue 7
, Pages
390-396
, September 2010
