Wnt Pathway Regulation of Lens Polarity
Wnt Pathway Regulation of Lens Polarity
批准号:
8227999
负责人:
Richard A. Lang
金额:
$38.25万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-09 至 2015-02-28
关键词:
AllelesAnteriorBiologyCellsComplexCoupledDataDevelopmentDiseaseEmbryonic DevelopmentEpithelialEpithelial CellsEpitheliumEquilibriumEyeFailureFamilyFamily memberFeedbackFunctional disorderGeneticGoalsHomeostasisLens FiberLigandsModelingMonitorMusMutateNamesOpticsOrganPathway interactionsPatternPhosphorylationProblem SolvingProductionRegulationRetinaRoleSignal PathwaySignal TransductionSourceT cell factor 3TestingTissuesWorkfiber cellhigh riskinnovationintercellular communicationlensloss of functionminimal riskpreventprogenitorpublic health relevancereceptorrecombinaseresearch studyresponsetooltranscription factortumor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Wnt pathways in lens polarity Wnt pathways are known to have a critical role in many aspects of development and disease. The long term goal of this competitive renewal application is an understanding of the role of Wnt pathways in regulating the epithelial to fiber cell transition and lens polarity during development. Preliminary studies show that when production of Wnt ligands is eliminated in the lens lineage, remarkably, lens epithelial cells differentiate into lens fiber cells. By contrast, when the Wnt pathway transcription factor Tcf3 is deleted conditionally in early lens, there is an opposite response where fiber cells fail to differentiate. These are surprising findings that underscore the importance of the Wnt/2-catenin pathway for regulating lens development and establishing the anterior epithelium-posterior fiber cell pattern that defines lens polarity. The function of this pathway in lens development has important implications for lens biology and perhaps for pathophysiologies where the epithelium is not maintained. Our central hypothesis is that The Wnt/2-catenin pathway regulates the epithelial-to-fiber cell transition to establish lens polarity. To investigate the validity of this hypothesis, we propose three Aims. 1. To determine the source of Wnt ligands crucial for establishing lens polarity. The mouse Wntless allele we have generated is very valuable because it is required for the activity of all Wnt ligands and thus solves the problem of how to generate a ligand loss-of-function when multiple ligands are expressed. We will take advantage of this allele, combined with different cre recombinase lines, to identify the source, or sources of Wnt ligands critical for the epithelial-to-fiber cell transition and lens polarity. 2. To determine whether non-canonical Wnt ligands provide negative-feedback regulation of the lens epithelial Wnt response. It has recently been shown that some Wnt ligands function only in the non-canonical pathways and furthermore, that they can block Wnt/2-catenin signaling by preventing the association of the Lrp5/6 co-receptors with Frizzleds. When coupled with the observation that several non-canonical ligands are expressed in lens fiber cells, this suggests that they may serve to down-regulate Wnt/2-catenin signaling after fiber cells have made contact with the epithelium. 3: To determine whether lens repolarization requires reactivation of the canonical Wnt pathway. In 1963, Coulombre and Coulombre performed the now classical experiment showing that a reversed chick lens (epithelium facing the retina) would re-polarize over the course of 10 days. As shown in our preliminary data, disruption of the Wnt pathway disrupts lens polarity suggesting that the Wnt pathway may be re-activated during re-polarization. We will test this hypothesis by monitoring and modulating the Wnt pathway during chick lens re-polarization. Combined, these studies will provide an in- depth assessment of the role of the Wnt pathway in lens development and overall, an important step forward in our understanding of this unique organ.
PUBLIC HEALTH RELEVANCE: In this application, we propose the study a cell-cell signaling pathway, the so-called Wnt pathway that is known to be critical for embryonic development, for tissue homeostasis and for the development of tumors. We will determine whether the Wnt pathway is responsible for determining the orientation of the lens within the eye and thus, whether this pathway is important for the unique optical capability of this organ.
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专著(0)
科研奖励(0)
会议论文
Melanopsin-dependent light-evoked development of rod photoreceptors
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批准号:10735293
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项目类别:
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资助金额:$40.13万
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财政年份:2023
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负责人:Richard A. Lang
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依托单位:
Mechanisms of intrinsic light responses in the ocular lens
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批准号:10426249
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项目类别:
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资助金额:$37.12万
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财政年份:2021
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负责人:Richard A. Lang
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依托单位:
Light regulated vascular development in the eye via the Hippo pathway
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批准号:10322455
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项目类别:
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资助金额:$41.94万
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财政年份:2021
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负责人:Richard A. Lang
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依托单位:
Mechanisms of intrinsic light responses in the ocular lens
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批准号:10636950
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项目类别:
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资助金额:$38.18万
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财政年份:2021
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负责人:Richard A. Lang
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依托单位:
Light regulated vascular development in the eye via the Hippo pathway
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批准号:10544744
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项目类别:
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资助金额:$43.23万
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财政年份:2021
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负责人:Richard A. Lang
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依托单位:
Regulation of vascular development in the eye by an opsin 5-dependent clock
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批准号:9769754
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项目类别:
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资助金额:$47.86万
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财政年份:2016
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负责人:Richard A. Lang
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依托单位:
Regulation of vascular development in the eye by an opsin 5-dependent clock
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批准号:9336304
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项目类别:
-
资助金额:$47.86万
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财政年份:2016
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负责人:Richard A. Lang
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依托单位:
Regulation of vascular development in the eye by an opsin 5-dependent clock
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批准号:9551622
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项目类别:
-
资助金额:$47.86万
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财政年份:2016
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负责人:Richard A. Lang
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依托单位:
Retinal Microglia and Angiogenesis
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批准号:8310517
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项目类别:
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资助金额:$38.25万
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财政年份:2012
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负责人:Richard A. Lang
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依托单位:
Retinal Microglia and Angiogenesis
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批准号:8461948
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项目类别:
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资助金额:$36.34万
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财政年份:2012
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负责人:Richard A. Lang
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依托单位:
Retinal Microglia and Angiogenesis
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批准号:8658090
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项目类别:
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资助金额:$37.49万
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财政年份:2012
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负责人:Richard A. Lang
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依托单位:
RhoGTPases in Early Eye Development
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批准号:7178055
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项目类别:
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资助金额:$30.0万
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财政年份:2007
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负责人:Richard A. Lang
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依托单位:
RhoGTPases in Early Eye Development
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批准号:7394331
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项目类别:
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资助金额:$29.4万
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财政年份:2007
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负责人:Richard A. Lang
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依托单位:
RhoGTPases in Early Eye Development
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批准号:8035896
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项目类别:
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资助金额:$32.08万
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财政年份:2007
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负责人:Richard A. Lang
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依托单位:
RhoGTPases in Early Eye Development
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批准号:7583884
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项目类别:
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资助金额:$33.75万
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财政年份:2007
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负责人:Richard A. Lang
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依托单位:
RhoGTPases in Early Eye Development
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批准号:7796663
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项目类别:
-
资助金额:$33.41万
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财政年份:2007
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负责人:Richard A. Lang
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依托单位:
Developing vision: Cadherin function in lens morphogenesis
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批准号:7121099
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项目类别:
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资助金额:$36.62万
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财政年份:2005
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负责人:Richard A. Lang
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依托单位:
Developing vision: Cadherin function in lens morphogenesis
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批准号:7487745
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项目类别:
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资助金额:$35.69万
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财政年份:2005
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负责人:Richard A. Lang
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依托单位:
Wnt Pathway Regulation of Lens Polarity
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批准号:8625305
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项目类别:
-
资助金额:$37.49万
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财政年份:2005
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负责人:Richard A. Lang
-
依托单位:
Wnt Pathway Regulation of Lens Polarity
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批准号:8435500
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项目类别:
-
资助金额:$36.34万
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财政年份:2005
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负责人:Richard A. Lang
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依托单位:
海外基金