Calcium-based Dendritic Excitability and Its Regulation in the 5 Deep Cerebellar Nuclei

نویسندگان

  • Eugene F. Civillico
  • Samuel S.-H. Wang
  • Eve Schneider
  • Eugene Civillico
چکیده

1 2 3 4 CALCIUM-BASED DENDRITIC EXCITABILITY AND ITS REGULATION IN THE 5 DEEP CEREBELLAR NUCLEI 6 7 Eve R. Schneider*, Eugene F. Civillico, Samuel S.-H. Wang 8 9 Department of Psychology, Department of Molecular Biology, and Princeton Neuroscience 10 Institute, Princeton University 11 12 13 14 Author contributions: 15 Eve Schneider, Eugene Civillico and Sam Wang designed the experiments. 16 Eve Schneider and Eugene Civillico performed the experiments. 17 Eve Schneider, Eugene Civillico and Sam Wang analyzed the data. 18 Eve Schneider, Eugene Civillico and Sam Wang wrote the paper. 19 20 Corresponding author: Samuel S.-H. Wang 21 Address: Department of Molecular Biology, Lewis Thomas Laboratory, Washington Road, 22 Princeton University, Princeton NJ, 08544. 23 *Current address: Department of Cellular & Molecular Physiology, Sterling Hall of Medicine, B24 Wing, 333 Cedar Street Room 156, Yale School of Medicine, New Haven, CT 06510. 25 26 Running head: Regulation of calcium spikes in DCN dendrites 27 28

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Contribution of Somatic and Dendritic SK Channels in the Firing Rate of Deep Cerebellar Nuclei: Implication in Cerebellar Ataxia

Introduction: Loss of inhibitory output from Purkinje cells leads to hyperexcitability of the Deep Cerebellar Nuclei (DCN), which results in cerebellar ataxia. Also, inhibition of small-conductancecalcium-activated potassium (SK) channel increases firing rate  f DCN, which could cause cerebellar ataxia. Therefore, SK channel activators can be effective in reducing the symptoms of this disease, ...

متن کامل

Calcium-based dendritic excitability and its regulation in the deep cerebellar nuclei.

The deep cerebellar nuclei (DCN) convey the final output of the cerebellum and are a major site of activity-dependent plasticity. Here, using patch-clamp recording and two-photon calcium imaging in rat brain slices, we demonstrate that DCN dendrites exhibit three hallmarks of active amplification of electrical signals. First, they produce calcium transients with rise times of tens of millisecon...

متن کامل

Contribution of Somatic and Dendritic SK Channels in the Firing Rate of Deep Cerebellar Nuclei: Implication in Cerebellar Ataxia

INTRODUCTION Loss of inhibitory output from Purkinje cells leads to hyperexcitability of the Deep Cerebellar Nuclei (DCN), which results in cerebellar ataxia. Also, inhibition of small-conductance calcium-activated potassium (SK) channel increases firing rate of DCN, which could cause cerebellar ataxia. Therefore, SK channel activators can be effective in reducing the symptoms of this disease, ...

متن کامل

Dendritic calcium spikes are tunable triggers of cannabinoid release and short-term synaptic plasticity in cerebellar Purkinje neurons.

Understanding the relationship between dendritic excitability and synaptic plasticity is vital for determining how dendrites regulate the input-output function of the neuron. Dendritic calcium spikes have been associated with the induction of long-term changes in synaptic efficacy. Here we use direct recordings from cerebellar Purkinje cell dendrites to show that synaptically activated local de...

متن کامل

Kv3.3b: a novel Shaw type potassium channel expressed in terminally differentiated cerebellar Purkinje cells and deep cerebellar nuclei.

A two-step hybridization/subtraction procedure was employed to isolate markers for the later stages of Purkinje cell differentiation. From this screen, a novel Shaw potassium channel cDNA (Kv3.3b) was identified that is developmentally regulated. Expression of this channel is highly enriched in the brain, particularly in the cerebellum, where its expression is confined to Purkinje cells and dee...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2013