ipRGC participation and modulation of retinal wave activity
ipRGC participation and modulation of retinal wave activity
批准号:
8326716
负责人:
Jordan Michael Renna
金额:
$5.57万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-08-03 至 2013-08-02
关键词:
AdultAffectBackCell physiologyCellsCircadian RhythmsDataDevelopmentInjuryJet Lag SyndromeLateral Geniculate BodyLightMalignant NeoplasmsMapsMediatingNicotinic ReceptorsPerformancePhotoreceptorsPlayPopulationPublic HealthPupil light reflexRegulationRetinaRetinalRetinal ConeRetinal Ganglion CellsRiskRoleSeasonal Affective DisorderSignal TransductionStagingSynapsesTestingTimeblindelectrical propertyfeedingganglion cellmelanopsinnovelphotoactivationpresynapticpublic health relevanceresponseretinal rodsretinotopicsegregationshift worksuperior colliculus Corpora quadrigeminavision development
中文摘要
描述(由申请人提供):
视网膜波包括跨越未成熟视网膜传播的自发激活区。这些波被认为参与视网膜定位图的发展和双眼输入到上级丘和外侧膝状体核的分离。视网膜波发生在视杆和视锥光感受器成熟之前,此时视网膜被认为对光不敏感。然而,最近的研究结果推翻了这一假设。有一类新的光感受器,即内在光敏视网膜神经节细胞(ipRGC),在此阶段功能完全。事实上,人们对ipRGC、光暴露和视网膜波之间可能的相互作用一无所知。这项提议不仅探讨了这些光感受器如何受到视网膜波的影响,而且还探讨了它们如何反过来影响视网膜波。在成人视网膜中,ipRGC不仅接收兴奋性和抑制性突触输入,而且被认为将信号反馈到内层视网膜中。这提高了视网膜波和ipRGC之间双向相互作用的可能性,尽管在这个发育阶段ipRGC的视网膜内突触连接尚未确定。初步数据表明,不仅ipRGC放电与视网膜波相关,而且这类神经节细胞的光激活改变视网膜波活动。因此,本提案的具体目标是:1.表征视网膜波活动期间ipRGC的激发并鉴定激活的机制; 2.检验光诱导的ipRGC激活改变视网膜波活动的假设,并评估相关机制。这些研究将为视网膜波活动的机制提供新的线索,并将扩展我们对ipRGC的理解,ipRGC在昼夜节律光诱导和瞳孔光反射中起着指导作用。
公共卫生相关性:
本研究将探讨一类特殊的视网膜细胞在正常视觉系统发育的调节中的作用。此外,它将为这些细胞在发育早期的功能提供新的线索。这些细胞在成年人身体对日光的反应中起着核心作用,因此,这些研究与诸如时差反应,季节性情感障碍,盲人昼夜节律紊乱以及轮班工作的负面后果(包括表现受损,受伤风险增加甚至癌症发病率升高)等公共卫生问题有关。
英文摘要
DESCRIPTION (provided by applicant):
Retinal waves comprise zones of spontaneous activation that propagate across the immature retina. These waves are thought to participate in the development of retinotopic maps and the segregation of binocular inputs to the superior colliculus and lateral geniculate nucleus. Retinal waves occur before rod and cone photoreceptors are mature, at a time when the retina has been considered insensitive to light. However, recent findings invalidate this assumption. There is a novel class of photoreceptor, the intrinsically photosensitive retinal ganglion cell (ipRGC), that is fully functional at this stage. Virtually nothing is known about possible interactions between ipRGCs, light exposure, and retinal waves. This proposal explores not only how these photoreceptors are affected by retinal waves, but also how they, in turn, may affect the waves. In the adult retina, ipRGCs not only receive excitatory and inhibitory synaptic input, but also are thought to feed signals back into the inner retina. This raises the possibility of bidirectional interactions between retinal waves and ipRGCs, although the intraretinal synaptic connectivity of ipRGCs at this developmental stage has not been determined. Preliminary data indicate that not only do ipRGCs discharge in association with retinal waves, but also that photic activation of this class of ganglion cells alters retinal wave activity. Therefore, the specific aims of this proposal are: 1. Characterize excitation of ipRGCs during retinal wave activity and identify the mechanism of activation; 2. Test the hypothesis that light-induced activation of ipRGCs alters retinal wave activity and assess the mechanism responsible. These studies will shed new light on the mechanism of retinal wave activity and will extend our understanding of ipRGCs, which play an instructive role in circadian rhythm photoentrainment and the pupillary light reflex.
PUBLIC HEALTH RELEVANCE:
This study will examine the role of a specialized class of retinal cells in the regulation of normal visual system development. Further, it will shed new light on how these cells function early in development. These cells play a central role in the adult body's response to daylight and therefore, these studies are relevant to such public health issues as jet lag, seasonal affective disorder, circadian disruption in the blind, and the negative consequences of shift work including impaired performance, increased risk of injury and even elevated cancer rates.
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会议论文
Novel tools for screening retinal function using improved human retinal organoid models
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批准号:10462668
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项目类别:
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资助金额:$11.3万
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财政年份:2021
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负责人:Jordan Michael Renna
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依托单位:
Novel tools for screening retinal function using improved human retinal organoid models
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批准号:10288593
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项目类别:
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资助金额:$31.98万
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财政年份:2021
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负责人:Jordan Michael Renna
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依托单位:
ipRGC participation and modulation of retinal wave activity
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批准号:8216456
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项目类别:
-
资助金额:$5.3万
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财政年份:2010
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负责人:Jordan Michael Renna
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依托单位:
ipRGC participation and modulation of retinal wave activity
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批准号:7998894
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项目类别:
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资助金额:$5.05万
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财政年份:2010
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负责人:Jordan Michael Renna
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依托单位:
海外基金