Ras and Phosphoinositide 3-kinase Signaling in Lens Development
Ras and Phosphoinositide 3-kinase Signaling in Lens Development
批准号:
8529686
负责人:
LIXING W RENEKER
金额:
$7.5万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-08-01 至 2013-11-30
关键词:
AddressAnimalsApoptosisApplications GrantsBiohazardous SubstanceBiologicalBudgetsCaringCataract ExtractionCell DeathCell Differentiation processCell ProliferationCell SurvivalCellsComplicationCore FacilityDevelopmentDiseaseDominant-Negative MutationEnvironmentEvaluationEventFGFR2 geneFiberFibroblast Growth Factor ReceptorsFundingGTP-Binding ProteinsGrantGrowth FactorInformation ServicesInstructionInsulinInvestigationKnockout MiceKnowledgeMalignant NeoplasmsMethodsMissouriMouse, Founder, TransgenicMusNuclearPAC1 phosphatasePathway interactionsPatternPhosphatidylinositolsPhosphoric Monoester HydrolasesPhosphotransferasesPlayProcessProductivityPublished CommentRas Signaling PathwayReceptor Protein-Tyrosine KinasesReceptor SignalingRecommendationRequest for ApplicationsResearchResearch PersonnelResource SharingRestRoleServicesSignal PathwaySignal TransductionStructureStudy SectionSystemTechnologyTimeTransgenic AnimalsTransgenic MiceTransgenic OrganismsVertebratesWorkanimal breedingfiber cellhuman subject protectioninnovationinsightlensmeetingsmethod developmentmouse modeloverexpressionpreventpromoterresearch studyweb site
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Lens cell proliferation, differentiation and survival are tightly regulated to achieve the normal developmental pattern and structure of the lens. Growth factors are likely the key regulators of these cellular events, but very little is known about the growth factor signaling pathways in the lens. Ras is a small GTP-binding protein downstream of growth factor receptor tyrosine kinases (RTKs) and plays a critical role in growth factor signaling. In the last grant period, we demonstrated that Ras is required for cell proliferation but not for the initiation of fiber cell differentiation during normal lens development. Other investigators have shown that signals activated by fibroblast growth factor receptors (FGFRs) are essential for fiber cell differentiation and lens cell survival. In this grant application, we will continue our investigation of the RTK-Ras signaling pathway in the lens. In Specific Aim 1 and 2, experiments are proposed to determine the role of Sprouty and ERK in lens development. Sprouty is a negative regulator of the RTK-Ras pathway and ERK is a downstream effector of Ras. In Specific Aim 3, we will explore the cell death mechanisms induced by FGFR signaling deficiency in mouse lens. The proposed experiments will provide further insights into potential ways to block lens cell proliferation and eliminate aberrant cells in the lens. Such knowledge is important for the development of methods to prevent and treat posterior capsular opacification (PCO), the most common complication of cataract surgery. Moreover, the results of this work will expand our understanding of growth factor signaling in cell proliferation and cell survival in other developmental systems and disease processes such as cancer. The purpose of this study is to investigate growth factor signaling in the developing mouse lens. This knowledge will help to develop new methods to prevent and treat posterior capsular opacification (PCO), the most common complication of cataract surgery.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1371/journal.pone.0117089
发表时间:
2015
期刊:
PloS one
影响因子:
3.7
作者:
[Zhang J, Upadhya D, Lu L, Reneker LW]
通讯作者:
Reneker LW
DOI:
10.1242/dev.081042
发表时间:
2013-04-01
期刊:
DEVELOPMENT
影响因子:
4.6
作者:
[Upadhya, Dinesh, Ogata, Masato, Reneker, Lixing W.]
通讯作者:
Reneker, Lixing W.
Programmed Cell Death in Anterior Eye Development and Peters' Anomaly
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批准号:8781813
-
项目类别:
-
资助金额:$38.38万
-
财政年份:2014
-
负责人:LIXING W RENEKER
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依托单位:
Programmed Cell Death in Anterior Eye Development and Peters' Anomaly
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批准号:9310279
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项目类别:
-
资助金额:$38.38万
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财政年份:2014
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负责人:LIXING W RENEKER
-
依托单位:
Ras & PI 3-Kinase Signaling in Lens Development
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批准号:7292135
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项目类别:
-
资助金额:$3.74万
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财政年份:2001
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负责人:LIXING W RENEKER
-
依托单位:
Ras & PI 3-Kinase Signaling in Lens Development
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批准号:6395301
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项目类别:
-
资助金额:$32.88万
-
财政年份:2001
-
负责人:LIXING W RENEKER
-
依托单位:
Ras and Phosphoinositide 3-kinase Signaling in Lens Development
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批准号:7742145
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项目类别:
-
资助金额:$36.02万
-
财政年份:2001
-
负责人:LIXING W RENEKER
-
依托单位:
Ras and Phosphoinositide 3-kinase Signaling in Lens Development
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批准号:7367534
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项目类别:
-
资助金额:$34.65万
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财政年份:2001
-
负责人:LIXING W RENEKER
-
依托单位:
Ras & PI 3-Kinase Signaling in Lens Development
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批准号:6637203
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项目类别:
-
资助金额:$25.38万
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财政年份:2001
-
负责人:LIXING W RENEKER
-
依托单位:
Ras & PI 3-Kinase Signaling in Lens Development
-
批准号:6525071
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项目类别:
-
资助金额:$25.38万
-
财政年份:2001
-
负责人:LIXING W RENEKER
-
依托单位:
Ras & PI 3-Kinase Signaling in Lens Development
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批准号:6782670
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项目类别:
-
资助金额:$25.38万
-
财政年份:2001
-
负责人:LIXING W RENEKER
-
依托单位:
Ras and Phosphoinositide 3-kinase Signaling in Lens Development
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批准号:7995197
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项目类别:
-
资助金额:$34.58万
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财政年份:2001
-
负责人:LIXING W RENEKER
-
依托单位:
Ras and Phosphoinositide 3-kinase Signaling in Lens Development
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批准号:7534777
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项目类别:
-
资助金额:$36.39万
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财政年份:2001
-
负责人:LIXING W RENEKER
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依托单位:
STUDYING MOLECULAR MECHANISMS OF EYE DEVELOPMENT USING TRANSGENIC MICE
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批准号:6221079
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项目类别:
-
资助金额:$0.13万
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财政年份:1999
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负责人:LIXING W RENEKER
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依托单位:
TGF ALPHA AND OCULAR MORPHOGENESIS
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批准号:2160528
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项目类别:
-
资助金额:$3.12万
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财政年份:1996
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负责人:LIXING W RENEKER
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依托单位:
TGF ALPHA AND OCULAR MORPHOGENESIS
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批准号:2160527
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项目类别:
-
资助金额:$2.99万
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财政年份:1995
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负责人:LIXING W RENEKER
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依托单位:
TGF ALPHA AND OCULAR MORPHOGENESIS
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批准号:2160526
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项目类别:
-
资助金额:$2.86万
-
财政年份:1995
-
负责人:LIXING W RENEKER
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依托单位:
海外基金