Abstract

The activity of Ca(2+)/calmodulin-dependent protein kinase IV (CaMKIV) is sensitive to activity-dependent changes in the level of intracellular Ca(2+). Following neuronal stimulation, the activation of CaMKIV may trigger synaptic modifications and transcriptional responses, both of which are involved in regulating cognitive and emotional behavior. Here, we used CaMKIV knockout (KO) neurons and mice to examine the function of CaMKIV in Ca(2+)-stimulated intracellular signaling and animal behavior, respectively. Following NMDA receptor activation or membrane depolarization, the up-regulation of CREB (cAMP responsive element binding protein) and its target gene Bdnf (brain-derived neurotrophic factor) was intact in cortical neurons obtained from CaMKIV KO mice. CaMKIV KO mice displayed severe impairment in contextual fear memory but normal locomotor activity and anxiety level in the contextual training chamber. Although CaMKIV KO mice showed normal memory in the standard passive avoidance task, they were defective in learning the temporal dissociative passive avoidance task. As indicated by the light/dark test and marble-burying test data, CaMKIV KO mice showed less anxiety and normal perseveration. In the voluntary wheel-running test, CaMKIV KO mice showed normal running time and distance but higher maximal running speed. Our results demonstrate the function of CaMKIV in regulating different forms of fear memory, anxiety, and certain aspect of motor function.

Highlights

  • The activity of Ca2+/calmodulin-dependent protein kinase IV (CaMKIV) is sensitive to activity-dependent changes in the level of intracellular Ca2+

  • We examined the function of CaMKIV in CREB phosphorylation and Bdnf transcription following the activation of the NMDA receptors (NMDAR) and the L-type voltage-gated calcium channels (L-VGCC)

  • 2.1 Genetic deletion of CaMKIV does not affect CREB phosphorylation and Bdnf transcription following the activation of NMDAR and L-VGCC

Read more

Summary

Introduction

The activity of Ca2+/calmodulin-dependent protein kinase IV (CaMKIV) is sensitive to activity-dependent changes in the level of intracellular Ca2+. The activation of CaMKIV may trigger synaptic modifications and transcriptional responses, both of which are involved in regulating cognitive and emotional behavior. Following NMDA receptor activation or membrane depolarization, the up-regulation of CREB (cAMP responsive element binding protein) and its target gene Bdnf (brain-derived neurotrophic factor) was intact in cortical neurons obtained from CaMKIV KO mice. Consistent with the notion that the CREB-mediated transcription is critical for neuroplasticity and adaptive behaviors, loss of activity-dependent CREB phosphorylation in CaMKIV KO mice correlates with the impairment in long-term potentiation (LTP) [10] and defective fear memory [10]. We examined the function of CaMKIV in CREB phosphorylation and Bdnf transcription following the activation of the NMDA receptors (NMDAR) and the L-type voltage-gated calcium channels (L-VGCC). Our data help to consolidate some inconsistent results from the previous studies

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call