Nonbinary branching of myelinated dendrites at nodal networks on afferent terminal arbors in paddlefish electroreceptors

D. F. Russell, Desmon E. Rogers, Lilia L. Neiman
{"title":"Nonbinary branching of myelinated dendrites at nodal networks on afferent terminal arbors in paddlefish electroreceptors","authors":"D. F. Russell, Desmon E. Rogers, Lilia L. Neiman","doi":"10.19185/MATTERS.201812000003","DOIUrl":null,"url":null,"abstract":"The branching of vertebrate neuronal processes, axons or dendrites, is predominantly binary, where a proximal neuronal process bifurcates into two distal progeny. Here, we illustrate counterexamples where neuronal processes branched into more than 2, up to 6, progeny branches, in one step. These were branch points of myelinated dendrites in the peripheral terminals of ALLn cranial nerve afferents innervating the Lorenziniantype ampullary electroreceptors on the rostrum of paddlefish, Polyodon spathula. We imaged afferent terminals fluorescently (in widefield stacks, with deconvolution) after immunolabling of afferent terminals for neuronal cytoplasmic neurofilament-H (NEFH), myelin markers (MBP, P0), or nodal ion channels (Nav1.x, Kv1.1), or after migration of DiI in dendrite membranes. Branched afferent terminals formed a laminar radial radiation beneath a receptive field, parallel to the skin surface, with two serial stages: (1) Starting at each afferent’s centric first branchpoint, each of a small group of 2–4 (most often 3) afferents branched radially into 2–4 (usually 3) generations of myelinated dendrites, whose internodes were covered by sheaths immunoreactive for antigenic markers of myelin (MBP+/P0+), ending distally at ~15 heminode presumed spike initiation zones. (2) From the latter, bundles of unmyelinated (MBP-/P0-) sensory neuron (NEFH+) processes projected distally to innervate electrosensory neuroepithelia of adjacent ampullary organs. The nonbinary branch points that we imaged were in stage-1, on myelinated dendrites. Branch points always coincided with composite systems of nodes, in which each progeny dendrite started at a narrowed nodal segment expressing voltage gated sodium ion channels at high density. These narrowed nodal segments of multiple progeny branched in parallel from a parent’s blunt distal end. Hence the branch point nodal complexes formed multisite excitable systems, likely strongly coupled due to proximity.","PeriodicalId":90172,"journal":{"name":"Grief matters","volume":"29 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Grief matters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19185/MATTERS.201812000003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

The branching of vertebrate neuronal processes, axons or dendrites, is predominantly binary, where a proximal neuronal process bifurcates into two distal progeny. Here, we illustrate counterexamples where neuronal processes branched into more than 2, up to 6, progeny branches, in one step. These were branch points of myelinated dendrites in the peripheral terminals of ALLn cranial nerve afferents innervating the Lorenziniantype ampullary electroreceptors on the rostrum of paddlefish, Polyodon spathula. We imaged afferent terminals fluorescently (in widefield stacks, with deconvolution) after immunolabling of afferent terminals for neuronal cytoplasmic neurofilament-H (NEFH), myelin markers (MBP, P0), or nodal ion channels (Nav1.x, Kv1.1), or after migration of DiI in dendrite membranes. Branched afferent terminals formed a laminar radial radiation beneath a receptive field, parallel to the skin surface, with two serial stages: (1) Starting at each afferent’s centric first branchpoint, each of a small group of 2–4 (most often 3) afferents branched radially into 2–4 (usually 3) generations of myelinated dendrites, whose internodes were covered by sheaths immunoreactive for antigenic markers of myelin (MBP+/P0+), ending distally at ~15 heminode presumed spike initiation zones. (2) From the latter, bundles of unmyelinated (MBP-/P0-) sensory neuron (NEFH+) processes projected distally to innervate electrosensory neuroepithelia of adjacent ampullary organs. The nonbinary branch points that we imaged were in stage-1, on myelinated dendrites. Branch points always coincided with composite systems of nodes, in which each progeny dendrite started at a narrowed nodal segment expressing voltage gated sodium ion channels at high density. These narrowed nodal segments of multiple progeny branched in parallel from a parent’s blunt distal end. Hence the branch point nodal complexes formed multisite excitable systems, likely strongly coupled due to proximity.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
白鲟电感受器传入末端乔木节点网络中有髓鞘树突的非二元分支
脊椎动物神经突的分支,轴突或树突,主要是二元的,其中一个近端神经元突分岔成两个远端后代。在这里,我们举例说明反例,其中神经元过程分支成2个以上,最多6个,子分支,在一个步骤。这些是支配白鲟喙部lorenzinia型壶腹电感受器的ALLn颅神经传入神经末梢有髓鞘树突的分支点。在神经细胞质神经丝- h (NEFH)、髓磷脂标记物(MBP、P0)或节离子通道(Nav1)免疫后,我们对传入终端进行荧光成像(宽视场堆栈,反卷积)。x, Kv1.1),或DiI在树突膜中迁移后。分支的传入神经末梢在感受野下形成层状径向辐射,平行于皮肤表面,有两个连续的阶段:(1)从每个传入神经的中心第一个分支点开始,每一个2-4(通常为3)个传入神经末梢径向分支成2-4(通常为3)代有髓鞘树突,其节间被对髓鞘抗原标记物(MBP+/P0+)具有免疫反应的鞘所覆盖,在远端结束于约15个半球处假定的尖峰起始区。(2)从后者,无髓鞘(MBP-/P0-)感觉神经元(NEFH+)突束向远端投射,支配邻近壶腹部器官的电感觉神经上皮。我们成像的非二元分支点处于1期,在有髓鞘的树突上。分支点总是与节点的复合系统重合,其中每个子代枝晶从一个狭窄的节点段开始,表达高密度的电压门控钠离子通道。多个子代的这些狭窄节段从亲本钝的远端平行分枝。因此,分支点节点复合物形成了多位点可激发系统,可能由于邻近而强耦合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
L’erreur française L’indemnisation des biens musicaux spoliés La loi électorale française parmi les difficultés de la Ve République Majorité Science, politique et engagement
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1