Suppr超能文献

Ephrin-A5 缺乏改变感觉运动和单胺能发育。

Ephrin-A5 deficiency alters sensorimotor and monoaminergic development.

机构信息

Departments of Chemical Biology, Susan Lehman-Cullman Laboratory for Cancer Research, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, NJ 08854, United States.

Environmental and Occupational Health Sciences Institute, a Joint Institute of Robert Wood Johnson Medical School and Rutgers University, Piscataway, NJ 08854, United States.

出版信息

Behav Brain Res. 2013 Jan 1;236(1):139-147. doi: 10.1016/j.bbr.2012.08.032. Epub 2012 Aug 27.

Abstract

The Eph receptors and their ligands, the ephrins, play an important role during neural development. In particular, ephrin-A5 is highly expressed in the developing nervous system in several brain regions including the olfactory bulb, frontal cortex, striatum and hypothalamus. Although a number of studies have characterized the expression of ephrin-A5 in these regions, very little is known about the functional consequences that might follow alterations in the expression of this ligand. Previously, we demonstrated that ephrin-A5 acts as a guidance molecule regulating the trajectory of the ascending midbrain dopaminergic pathways. In light of this finding and the critical role of dopamine in modulating a number of behaviors, we sought to determine whether loss of ephrin-A5 altered neurobehavioral development. Our results indicate that ephrin-A5-null mice exhibit delays in reaching developmental milestones and in the maturation of motor skills. In addition, they exhibit increased locomotor activity and reduced levels of brain monoamines. Therefore, we conclude that ephrin-A5 expression appears to be critical for proper development of central monoaminergic pathways and that its loss results in a number of neurodevelopmental abnormalities. Because alterations in monoamine function are associated with a variety of neurodevelopmental disorders, these data suggest that further study on the potential role of ephrin-A5 in such disorders is warranted.

摘要

Eph 受体及其配体 Ephrins 在神经发育过程中发挥着重要作用。特别是 Ephrin-A5 在包括嗅球、额叶皮质、纹状体和下丘脑在内的几个脑区的发育神经系统中高度表达。尽管许多研究已经描述了 Ephrin-A5 在这些区域的表达,但对于这种配体表达的改变可能带来的功能后果知之甚少。先前,我们证明 Ephrin-A5 作为一种指导分子,调节中脑多巴胺能通路的上升轨迹。鉴于这一发现以及多巴胺在调节许多行为中的关键作用,我们试图确定 Ephrin-A5 的缺失是否会改变神经行为发育。我们的研究结果表明, Ephrin-A5 缺失小鼠在达到发育里程碑和运动技能成熟方面存在延迟。此外,它们还表现出增加的运动活性和降低的脑单胺水平。因此,我们得出结论, Ephrin-A5 的表达似乎对中枢单胺能通路的正常发育至关重要,其缺失会导致多种神经发育异常。由于单胺功能的改变与多种神经发育障碍有关,这些数据表明,进一步研究 Ephrin-A5 在这些障碍中的潜在作用是有必要的。

相似文献

1
Ephrin-A5 deficiency alters sensorimotor and monoaminergic development.
Behav Brain Res. 2013 Jan 1;236(1):139-147. doi: 10.1016/j.bbr.2012.08.032. Epub 2012 Aug 27.
2
Ephrin-A5 modulates the topographic mapping and connectivity of commissural axons in murine hippocampus.
Neuroscience. 2006 Aug 11;141(1):109-21. doi: 10.1016/j.neuroscience.2006.03.052. Epub 2006 May 11.
3
Decreased maternal behavior and anxiety in ephrin-A5 mice.
Genes Brain Behav. 2017 Feb;16(2):271-284. doi: 10.1111/gbb.12319. Epub 2016 Sep 22.
4
The role of ephrin-A2 and ephrin-A5 in sensorimotor control and gating.
Behav Brain Res. 2014 Dec 15;275:225-33. doi: 10.1016/j.bbr.2014.08.061. Epub 2014 Sep 6.
5
Reduction of ephrin-A5 aggravates disease progression in amyotrophic lateral sclerosis.
Acta Neuropathol Commun. 2019 Jul 12;7(1):114. doi: 10.1186/s40478-019-0759-6.
6
Ephrin-A5 regulates the formation of the ascending midbrain dopaminergic pathways.
Dev Neurobiol. 2009 Jan;69(1):36-46. doi: 10.1002/dneu.20685.
9
Ephrin-A5 exerts positive or inhibitory effects on distinct subsets of EphA4-positive motor neurons.
J Neurosci. 2004 Feb 4;24(5):1070-8. doi: 10.1523/JNEUROSCI.4719-03.2004.

引用本文的文献

4
Decreased maternal behavior and anxiety in ephrin-A5 mice.
Genes Brain Behav. 2017 Feb;16(2):271-284. doi: 10.1111/gbb.12319. Epub 2016 Sep 22.
5
Comparative Proteomic Analysis of Carbonylated Proteins from the Striatum and Cortex of Pesticide-Treated Mice.
Parkinsons Dis. 2015;2015:812532. doi: 10.1155/2015/812532. Epub 2015 Aug 9.
8
Ephrin-A5 regulates inter-male aggression in mice.
Behav Brain Res. 2015 Jun 1;286:300-7. doi: 10.1016/j.bbr.2015.03.001. Epub 2015 Mar 6.
9
The Ephrin-A5/EphA4 Interaction Modulates Neurogenesis and Angiogenesis by the p-Akt and p-ERK Pathways in a Mouse Model of TLE.
Mol Neurobiol. 2016 Jan;53(1):561-576. doi: 10.1007/s12035-014-9020-2. Epub 2014 Dec 11.
10
Formation of persistent hyperplastic primary vitreous in ephrin-A5-/- mice.
Invest Ophthalmol Vis Sci. 2014 Mar 19;55(3):1594-606. doi: 10.1167/iovs.13-12706.

本文引用的文献

1
Astrocyte-specific disruption of SynCAM1 signaling results in ADHD-like behavioral manifestations.
PLoS One. 2012;7(4):e36424. doi: 10.1371/journal.pone.0036424. Epub 2012 Apr 30.
2
Ephrin reverse signaling in axon guidance and synaptogenesis.
Semin Cell Dev Biol. 2012 Feb;23(1):58-64. doi: 10.1016/j.semcdb.2011.10.024. Epub 2011 Oct 24.
3
Non-SH2/PDZ reverse signaling by ephrins.
Semin Cell Dev Biol. 2012 Feb;23(1):65-74. doi: 10.1016/j.semcdb.2011.10.012. Epub 2011 Oct 21.
4
Mesolimbic dopamine transients in motivated behaviors: focus on maternal behavior.
Front Psychiatry. 2011 May 9;2:23. doi: 10.3389/fpsyt.2011.00023. eCollection 2011.
5
Cingulate, frontal, and parietal cortical dysfunction in attention-deficit/hyperactivity disorder.
Biol Psychiatry. 2011 Jun 15;69(12):1160-7. doi: 10.1016/j.biopsych.2011.01.022. Epub 2011 Apr 13.
6
7
Motor cortex inhibition: a marker of ADHD behavior and motor development in children.
Neurology. 2011 Feb 15;76(7):615-21. doi: 10.1212/WNL.0b013e31820c2ebd.
8
Visual map development: bidirectional signaling, bifunctional guidance molecules, and competition.
Cold Spring Harb Perspect Biol. 2010 Nov;2(11):a001768. doi: 10.1101/cshperspect.a001768. Epub 2010 Sep 29.
9
EphrinA5 protein distribution in the developing mouse brain.
BMC Neurosci. 2010 Aug 25;11:105. doi: 10.1186/1471-2202-11-105.
10
Axon guidance molecules in vascular patterning.
Cold Spring Harb Perspect Biol. 2010 May;2(5):a001875. doi: 10.1101/cshperspect.a001875. Epub 2010 Mar 31.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验