钙传感器STIM1和STIM2调节培养海马神经元不同钙功能。

IF 2.8 4区 医学 Q2 NEUROSCIENCES
Frontiers in Synaptic Neuroscience Pub Date : 2021-01-05 eCollection Date: 2020-01-01 DOI:10.3389/fnsyn.2020.573714
Liliya Kushnireva, Eduard Korkotian, Menahem Segal
{"title":"钙传感器STIM1和STIM2调节培养海马神经元不同钙功能。","authors":"Liliya Kushnireva,&nbsp;Eduard Korkotian,&nbsp;Menahem Segal","doi":"10.3389/fnsyn.2020.573714","DOIUrl":null,"url":null,"abstract":"<p><p>There are growing indications for the involvement of calcium stores in the plastic properties of neurons and particularly in dendritic spines of central neurons. The store-operated calcium entry (SOCE) channels are assumed to be activated by the calcium sensor stromal interaction molecule (STIM)which leads to activation of its associated Orai channel. There are two STIM species, and the differential role of the two in SOCE is not entirely clear. In the present study, we were able to distinguish between transfected STIM1, which is more mobile primarily in young neurons, and STIM2 which is less mobile and more prominent in older neurons in culture. STIM1 mobility is associated with spontaneous calcium sparks, local transient rise in cytosolic [Ca<sup>2+</sup>]<sub>i</sub>, and in the formation and elongation of dendritic filopodia/spines. In contrast, STIM2 is associated with older neurons, where it is mobile and moves into dendritic spines primarily when cytosolic [Ca<sup>2+</sup>]<sub>i</sub> levels are reduced, apparently to activate resident Orai channels. These results highlight a role for STIM1 in the regulation of [Ca<sup>2+</sup>]<sub>i</sub> fluctuations associated with the <i>formation</i> of dendritic spines or filopodia in the developing neuron, whereas STIM2 is associated with the <i>maintenance</i> of calcium entry into stores in the adult neuron.</p>","PeriodicalId":12650,"journal":{"name":"Frontiers in Synaptic Neuroscience","volume":"12 ","pages":"573714"},"PeriodicalIF":2.8000,"publicationDate":"2021-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3389/fnsyn.2020.573714","citationCount":"9","resultStr":"{\"title\":\"Calcium Sensors STIM1 and STIM2 Regulate Different Calcium Functions in Cultured Hippocampal Neurons.\",\"authors\":\"Liliya Kushnireva,&nbsp;Eduard Korkotian,&nbsp;Menahem Segal\",\"doi\":\"10.3389/fnsyn.2020.573714\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>There are growing indications for the involvement of calcium stores in the plastic properties of neurons and particularly in dendritic spines of central neurons. The store-operated calcium entry (SOCE) channels are assumed to be activated by the calcium sensor stromal interaction molecule (STIM)which leads to activation of its associated Orai channel. There are two STIM species, and the differential role of the two in SOCE is not entirely clear. In the present study, we were able to distinguish between transfected STIM1, which is more mobile primarily in young neurons, and STIM2 which is less mobile and more prominent in older neurons in culture. STIM1 mobility is associated with spontaneous calcium sparks, local transient rise in cytosolic [Ca<sup>2+</sup>]<sub>i</sub>, and in the formation and elongation of dendritic filopodia/spines. In contrast, STIM2 is associated with older neurons, where it is mobile and moves into dendritic spines primarily when cytosolic [Ca<sup>2+</sup>]<sub>i</sub> levels are reduced, apparently to activate resident Orai channels. These results highlight a role for STIM1 in the regulation of [Ca<sup>2+</sup>]<sub>i</sub> fluctuations associated with the <i>formation</i> of dendritic spines or filopodia in the developing neuron, whereas STIM2 is associated with the <i>maintenance</i> of calcium entry into stores in the adult neuron.</p>\",\"PeriodicalId\":12650,\"journal\":{\"name\":\"Frontiers in Synaptic Neuroscience\",\"volume\":\"12 \",\"pages\":\"573714\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2021-01-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.3389/fnsyn.2020.573714\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Synaptic Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3389/fnsyn.2020.573714\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Synaptic Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fnsyn.2020.573714","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 9

摘要

越来越多的迹象表明,钙的储存与神经元的可塑性有关,特别是与中枢神经元的树突棘有关。储存操作钙进入(SOCE)通道被钙传感器基质相互作用分子(STIM)激活,从而导致其相关的Orai通道被激活。有两种STIM,两者在SOCE中的不同作用尚不完全清楚。在目前的研究中,我们能够区分转染的STIM1和STIM2,前者主要在年轻神经元中更具移动性,后者在培养的老年神经元中移动性较差,但更突出。STIM1迁移率与自发钙火花、细胞质[Ca2+]i的局部瞬时升高以及树突丝状足/棘的形成和伸长有关。相反,STIM2与较老的神经元有关,当细胞质[Ca2+]i水平降低时,STIM2是可移动的,主要移动到树突棘中,显然是为了激活常驻的Orai通道。这些结果强调了STIM1在调节与发育中的神经元树突棘或丝状足形成相关的[Ca2+]i波动中的作用,而STIM2与维持钙进入成年神经元中的储存有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Calcium Sensors STIM1 and STIM2 Regulate Different Calcium Functions in Cultured Hippocampal Neurons.

Calcium Sensors STIM1 and STIM2 Regulate Different Calcium Functions in Cultured Hippocampal Neurons.

Calcium Sensors STIM1 and STIM2 Regulate Different Calcium Functions in Cultured Hippocampal Neurons.

Calcium Sensors STIM1 and STIM2 Regulate Different Calcium Functions in Cultured Hippocampal Neurons.

There are growing indications for the involvement of calcium stores in the plastic properties of neurons and particularly in dendritic spines of central neurons. The store-operated calcium entry (SOCE) channels are assumed to be activated by the calcium sensor stromal interaction molecule (STIM)which leads to activation of its associated Orai channel. There are two STIM species, and the differential role of the two in SOCE is not entirely clear. In the present study, we were able to distinguish between transfected STIM1, which is more mobile primarily in young neurons, and STIM2 which is less mobile and more prominent in older neurons in culture. STIM1 mobility is associated with spontaneous calcium sparks, local transient rise in cytosolic [Ca2+]i, and in the formation and elongation of dendritic filopodia/spines. In contrast, STIM2 is associated with older neurons, where it is mobile and moves into dendritic spines primarily when cytosolic [Ca2+]i levels are reduced, apparently to activate resident Orai channels. These results highlight a role for STIM1 in the regulation of [Ca2+]i fluctuations associated with the formation of dendritic spines or filopodia in the developing neuron, whereas STIM2 is associated with the maintenance of calcium entry into stores in the adult neuron.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.10
自引率
2.70%
发文量
74
审稿时长
14 weeks
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信