Impaired dendritic spike generation in the Fragile X prefrontal cortex is due to loss of dendritic sodium channels

Author:

Brandalise Federico123,Kalmbach Brian E.1245,Cook Erik P.6ORCID,Brager Darrin H.12ORCID

Affiliation:

1. Center for Learning and Memory University of Texas at Austin Austin TX USA

2. Department of Neuroscience University of Texas at Austin Austin TX USA

3. Department of Biosciences University of Milan Milano Italy

4. Allen Institute for Brain Science Seattle WA USA

5. Department of Physiology and Biophysics University of Washington Seattle WA USA

6. Department of Physiology McGill University Montreal QC Canada

Abstract

AbstractPatients with Fragile X syndrome, the leading monogenetic cause of autism, suffer from impairments related to the prefrontal cortex, including working memory and attention. Synaptic inputs to the distal dendrites of layer 5 pyramidal neurons in the prefrontal cortex have a weak influence on the somatic membrane potential. To overcome this filtering, distal inputs are transformed into local dendritic Na+ spikes, which propagate to the soma and trigger action potential output. Layer 5 extratelencephalic (ET) prefrontal cortex (PFC) neurons project to the brainstem and various thalamic nuclei and are therefore well positioned to integrate task‐relevant sensory signals and guide motor actions. We used current clamp and outside‐out patch clamp recording to investigate dendritic spike generation in ET neurons from male wild‐type and Fmr1 knockout (FX) mice. The threshold for dendritic spikes was more depolarized in FX neurons compared to wild‐type. Analysis of voltage responses to simulated in vivo ‘noisy’ current injections showed that a larger dendritic input stimulus was required to elicit dendritic spikes in FX ET dendrites compared to wild‐type. Patch clamp recordings revealed that the dendritic Na+ conductance was significantly smaller in FX ET dendrites. Taken together, our results suggest that the generation of Na+‐dependent dendritic spikes is impaired in ET neurons of the PFC in FX mice. Considering our prior findings that somatic D‐type K+ and dendritic hyperpolarization‐activated cyclic nucleotide‐gated‐channel function is reduced in ET neurons, we suggest that dendritic integration by PFC circuits is fundamentally altered in Fragile X syndrome. imageKey points Dendritic spike threshold is depolarized in layer 5 prefrontal cortex neurons in Fmr1 knockout (FX) mice. Simultaneous somatic and dendritic recording with white noise current injections revealed that larger dendritic stimuli were required to elicit dendritic spikes in FX extratelencephalic (ET) neurons. Outside‐out patch clamp recording revealed that dendritic sodium conductance density was lower in FX ET neurons.

Funder

National Institutes of Health

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

Physiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3