J4 ›› 2011, Vol. 37 ›› Issue (6): 976-980.

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Calcium excitability of rat primary hippocampal neuron damaged by silenced retinoic acid receptor α

 JIANG Wei1,2,3, YU Qin1,2, GONG Min1,2, BI Yang1,2, ZHANG Zan1,2, CHEN Li1,2, QU Ping1,2, WEI Xiao-Ping1,2, LIU You-Xue1,2, CHEN Ji1,2, LI Ting-Yu1,2   

  1. (1. Children Nutrition Center,Children&rsquo|s Hospital,Chongqing Medical University,Chongqing 400014,China;2. Key Laboratory of Developmental Diseases in Childhood,Ministry of Education,Chongqing Medical University,Chongqing 400014,China;3. Rehabilitation Center,Children’s Hospital,Chongqing Medical University,Chongqing 400014|China)
  • Received:2011-06-29 Online:2011-11-28 Published:2011-11-28

Abstract:

bstract:Objective
To study the necessary of retinoic acid receptor α (RARα) for rat neuron function.
Methods Tissue digestion was used to isolate and cultivate the rat primary hippocampal neurons,and the adenovirus vector was used to  specifically silence the  RARα;Real-Time PCR was used to analyze the influence of silenced RARα in  retinoic acid(RA) receptors and the markers of nerve cells;live cell imaging analysis was performed to analyze the influence of the calcium excitability of neurons silenced RARα.Results The immunofluorescence results showed that  90% of the isolated cells expressed the  neuron marker neuron-specific enolase (NSE),the adenoviral transfection efficiency was up to 80%.The PCR results showed the expression of RARα in silenced RARα neuron was decreased by 75% (P<0.01),the other receptors were significantly decreased (P<0.01),but RARβ was significantly increased (P<0.05).The live cell calcium imaging results showed the calcium excitability in silent group was significantly reduced (P<0.05),however all-trans retinoic acid (ATRA) pretreatment for 24 h could significantly enhance the calcium excitability (P<0.01).Conclusion The absence of RARα can significantly reduce the neuron marker NSE expression of the primary hippocampal neurons,and significantly damage the neuronal calcium excitability.

Key words: primary hippocampal neurons;retinoic acid;retinoic acid receptor α;calcium excitability;gene silence

CLC Number: 

  • R338