Objective: To Observe the role of Notch signaling pathways in adult nerve regeneration.Method: Male mice of thirty five C57/BL were randomly divided into ischemia group,DAPT group (indicating ischemia and DAPT)and sham group. After middle cerebralocclusion(MCAO),experimental mice group were randomly injected DAPT and DMSO(100mg/kg)by intraperitoneal injection. Ten days after MCAO, the mices were injectedBrdU (50mg/kg)for three consecutive days. After12hours, sacrificing the mices,thehippocampus were dyed with GFAP/BrdU, DCX/BrdU immunofluorescence doublestandard to observe the changes of cells.Western Blot had test the change of the Notch1signaling proteins.The Real time PCR had detected Hes1relative expression ofmRNA.Result:After MCAO,among ischemia group, DAPT group (indicating ischemia andDAPT) and sham group,GFAP/BrdU, DCX/BrdU positive cells of ischemia group wassignificantly increased (P <0.01).Western Blot results suggest that ischemia can promoteNICD protein expression (P <0.01), DAPT can decrease the NICD protein expression (P<0.01).Real time PCR results indicate that the Hes1mRNA relative expression ofhippocampal tissue were significantly increased in ischemia group (P <0.01).Ischemia canpromote Hes1mRNA expression,but DAPT may reduce Hes1mRNA expression.,Conclusion: After cerebral ischemia Notch signaling is involved in the differentiation ofneural stem cells. |