Mukilan Murugan, Ragu Varman Durairaj, Sudhakar Sivasubramaniam, Rajan Koilmani Emmanuvel
Department of Animal Science, School of Life Sciences, Bharathidasan University, Tiruchirappalli 620024, India.
Department of Biotechnology, Manonmaniam Sundaranar University, Tirunelveli 627012, India.
Neurobiol Learn Mem. 2015 Apr;120:41-51. doi: 10.1016/j.nlm.2015.02.010. Epub 2015 Feb 25.
The activity-dependent expression of immediate-early genes (IEGs) and microRNA (miR)-132 has been implicated in synaptic plasticity and the formation of long-term memory (LTM). In the present study, we show that olfactory training induces the expression of IEGs (EGR-1, C-fos, C-jun) and miR-132 at similar time scale in olfactory bulb (OB) of Cynopterus sphinx. We examined the role of miR-132 in the OB using antisense oligodeoxynucleotide (AS-ODN) and demonstrated that a local infusion of AS-ODN in the OB 2h prior to training impaired olfactory memory formation in C. sphinx. However, the infusion of AS-ODN post-training did not cause a deficit in memory formation. Furthermore, the inhibition of miR-132 reduced the olfactory training-induced expression of IEGs and post synaptic density protein-95 (PSD-95) in the OB. Additionally, we show that miR-132 regulates the activation of calcium/calmodulin-dependent protein kinase-II (CaMKII) and cAMP response element binding protein (CREB), possibly through miR-148a. These data suggest that olfactory training induces the expression of miR-132 and IEGs, which in turn activates post-synaptic proteins that regulate olfactory memory formation.
即刻早期基因(IEGs)和微小RNA(miR)-132的活性依赖型表达与突触可塑性及长期记忆(LTM)的形成有关。在本研究中,我们发现嗅觉训练在短鼻果蝠嗅球(OB)中,在相似的时间尺度上诱导了IEGs(早期生长反应蛋白-1、C-Fos、C-Jun)和miR-132的表达。我们使用反义寡脱氧核苷酸(AS-ODN)研究了miR-132在嗅球中的作用,并证明在训练前2小时向嗅球局部注入AS-ODN会损害短鼻果蝠的嗅觉记忆形成。然而,训练后注入AS-ODN并未导致记忆形成缺陷。此外,抑制miR-132可降低嗅球中嗅觉训练诱导的IEGs和突触后致密蛋白95(PSD-95)的表达。此外,我们发现miR-132可能通过miR-148a调节钙/钙调蛋白依赖性蛋白激酶-II(CaMKII)和环磷酸腺苷反应元件结合蛋白(CREB)的激活。这些数据表明,嗅觉训练诱导了miR-132和IEGs的表达,进而激活了调节嗅觉记忆形成的突触后蛋白。