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驱动蛋白衔接蛋白钙结合蛋白-1在感觉轴突分支发育过程中组织微管极性并调节其动力学。

The Kinesin Adaptor Calsyntenin-1 Organizes Microtubule Polarity and Regulates Dynamics during Sensory Axon Arbor Development.

作者信息

Lee Tristan J, Lee Jacob W, Haynes Elizabeth M, Eliceiri Kevin W, Halloran Mary C

机构信息

Department of Zoology, University of Wisconsin-MadisonMadison, WI, USA.

Department of Neuroscience, University of Wisconsin-MadisonMadison, WI, USA.

出版信息

Front Cell Neurosci. 2017 Apr 20;11:107. doi: 10.3389/fncel.2017.00107. eCollection 2017.

DOI:10.3389/fncel.2017.00107
PMID:28473757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5397401/
Abstract

Axon growth and branching, and development of neuronal polarity are critically dependent on proper organization and dynamics of the microtubule (MT) cytoskeleton. MTs must organize with correct polarity for delivery of diverse cargos to appropriate subcellular locations, yet the molecular mechanisms regulating MT polarity remain poorly understood. Moreover, how an actively branching axon reorganizes MTs to direct their plus ends distally at branch points is unknown. We used high-speed, imaging of polymerizing MT plus ends to characterize MT dynamics in developing sensory axon arbors in zebrafish embryos. We find that axonal MTs are highly dynamic throughout development, and that the peripheral and central axons of sensory neurons show differences in MT behaviors. Furthermore, we show that Calsyntenin-1 (Clstn-1), a kinesin adaptor required for sensory axon branching, also regulates MT polarity in developing axon arbors. In wild type neurons the vast majority of MTs are directed in the correct plus-end-distal orientation from early stages of development. Loss of Clstn-1 causes an increase in MTs polymerizing in the retrograde direction. These misoriented MTs most often are found near growth cones and branch points, suggesting Clstn-1 is particularly important for organizing MT polarity at these locations. Together, our results suggest that Clstn-1, in addition to regulating kinesin-mediated cargo transport, also organizes the underlying MT highway during axon arbor development.

摘要

轴突的生长与分支以及神经元极性的发育,严重依赖于微管(MT)细胞骨架的正确组织和动态变化。微管必须以正确的极性进行组织,以便将各种货物运输到合适的亚细胞位置,然而调节微管极性的分子机制仍知之甚少。此外,活跃分支的轴突如何在分支点重新组织微管,以将其正端向远端引导,目前尚不清楚。我们利用高速成像技术观察聚合微管正端的动态变化,以表征斑马鱼胚胎发育中的感觉轴突分支中的微管动态。我们发现轴突微管在整个发育过程中高度动态,并且感觉神经元的外周和中枢轴突在微管行为上存在差异。此外,我们表明,钙结合蛋白-1(Clstn-1)是感觉轴突分支所需的驱动蛋白适配器,它也调节发育中的轴突分支中的微管极性。在野生型神经元中,从发育早期开始,绝大多数微管就以正确的正端向远端方向定向。Clstn-1的缺失导致逆行方向聚合的微管增加。这些方向错误的微管最常出现在生长锥和分支点附近,这表明Clstn-1对于在这些位置组织微管极性尤为重要。总之,我们的结果表明,Clstn-1除了调节驱动蛋白介导的货物运输外,还在轴突分支发育过程中组织潜在的微管通道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/3caa84277aab/fncel-11-00107-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/58bf4eee4d0e/fncel-11-00107-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/eafaac9b5abb/fncel-11-00107-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/02abaa260b0a/fncel-11-00107-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/5444eff6963d/fncel-11-00107-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/3caa84277aab/fncel-11-00107-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/58bf4eee4d0e/fncel-11-00107-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/eafaac9b5abb/fncel-11-00107-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/02abaa260b0a/fncel-11-00107-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/5444eff6963d/fncel-11-00107-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d66/5397401/3caa84277aab/fncel-11-00107-g0005.jpg

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本文引用的文献

1
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Proc Natl Acad Sci U S A. 2016 Mar 1;113(9):2418-23. doi: 10.1073/pnas.1520817113. Epub 2016 Feb 16.
2
Calsyntenin 1-mediated trafficking of axon guidance receptors regulates the switch in axonal responsiveness at a choice point.钙黏连蛋白1介导的轴突导向受体运输调控了轴突在选择点处反应性的转换。
Development. 2016 Mar 15;143(6):994-1004. doi: 10.1242/dev.127449. Epub 2016 Feb 2.
3
Dendrites In Vitro and In Vivo Contain Microtubules of Opposite Polarity and Axon Formation Correlates with Uniform Plus-End-Out Microtubule Orientation.
Res Sq. 2024 Sep 27:rs.3.rs-5006011. doi: 10.21203/rs.3.rs-5006011/v1.
4
Nageotte nodules in human DRG reveal neurodegeneration in painful diabetic neuropathy.人类背根神经节中的纳热奥特小结揭示了疼痛性糖尿病神经病变中的神经退行性变。
bioRxiv. 2024 Aug 23:2024.08.22.609215. doi: 10.1101/2024.08.22.609215.
5
KLC4 shapes axon arbors during development and mediates adult behavior.KLC4 塑造发育中的轴突分支,并介导成年行为。
Elife. 2022 Oct 12;11:e74270. doi: 10.7554/eLife.74270.
6
Phosphoregulation of Kinesins Involved in Long-Range Intracellular Transport.参与长距离细胞内运输的驱动蛋白的磷酸化调控
Front Cell Dev Biol. 2022 Jun 3;10:873164. doi: 10.3389/fcell.2022.873164. eCollection 2022.
7
A Model of Discovery: The Role of Imaging Established and Emerging Non-mammalian Models in Neuroscience.一种发现模式:成像技术在神经科学中已确立和新兴的非哺乳动物模型中的作用。
Front Mol Neurosci. 2022 Apr 14;15:867010. doi: 10.3389/fnmol.2022.867010. eCollection 2022.
8
Activation of the CaMKII-Sarm1-ASK1-p38 MAP kinase pathway protects against axon degeneration caused by loss of mitochondria.钙调蛋白激酶 II-Sarm1-ASK1-p38MAP 激酶通路的激活可防止因线粒体丧失引起的轴突变性。
Elife. 2022 Mar 14;11:e73557. doi: 10.7554/eLife.73557.
9
Microtubule organization of vertebrate sensory neurons in vivo.脊椎动物感觉神经元的微管组织。
Dev Biol. 2021 Oct;478:1-12. doi: 10.1016/j.ydbio.2021.06.007. Epub 2021 Jun 18.
10
Trim9 and Klp61F promote polymerization of new dendritic microtubules along parallel microtubules.Trim9 和 Klp61F 促进新的树突状微管沿着平行微管进行聚合。
J Cell Sci. 2021 Jun 1;134(11). doi: 10.1242/jcs.258437. Epub 2021 Jun 7.
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J Neurosci. 2016 Jan 27;36(4):1071-85. doi: 10.1523/JNEUROSCI.2430-15.2016.
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Neuron. 2015 Dec 16;88(6):1208-1226. doi: 10.1016/j.neuron.2015.11.012. Epub 2015 Dec 6.
5
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Elife. 2015 Dec 28;4:e10140. doi: 10.7554/eLife.10140.
6
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Nat Neurosci. 2015 Oct;18(10):1437-45. doi: 10.1038/nn.4099. Epub 2015 Aug 31.
7
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J Neurosci. 2014 Jul 9;34(28):9235-48. doi: 10.1523/JNEUROSCI.0561-14.2014.
10
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J Neurosci. 2014 Jun 25;34(26):8716-27. doi: 10.1523/JNEUROSCI.0144-14.2014.