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Fig. 7. Treatment of retina cells with SFRP1 is associated with phospho-Ser9-mediated inhibition of GSK3ß activity. (A) SFRP1-inhibits GSK3ß activity by phosphorylation at Ser9. SFRP1- or control-treated retina cells, harvested three or five hours after the culture, were analysed by immunoblots with antibodies {alpha}-GSK3ß-phospho-Ser9 (inactive form), GSK3ß-phospho-Tyr216 (active form) and {alpha}-tubulin, as loading control. NDV indicate a clear increase in phospho-Ser9-mediated inhibition of GSK3ß activity. (B) The total and phospho-Ser9-fraction of GSK3ß was evaluated with specific antibodies by western blots in retina explants electroporated with either Gfp or Sfrp1-myc and collected five hours after protein expression. Total content of GSK3ß was normalised against {alpha}-tubulin. Phospho-Ser9 positive bands were normalised against total GSK3ß content. Anti-myc demonstrates Sfrp1-myc expression after electroporation.





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