Permeability of Lens Gap Junction Channels
透镜间隙连接通道的磁导率
基本信息
- 批准号:10200058
- 负责人:
- 金额:$ 33.79万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-08-15 至 2023-06-30
- 项目状态:已结题
- 来源:
- 关键词:3-DimensionalAgeAgingAntioxidantsBiological AssayCataractCataract ExtractionCell NucleusCellsCommunicationComplementConnexinsCouplingDataDevelopmentDiffuseDiffusionDiseaseEconomic BurdenElectrophysiology (science)EnvironmentExhibitsGap JunctionsGlutathioneGlutathione DisulfideGlutathione ReductaseHealthcare SystemsHumanImageIntercellular JunctionsIon TransportKineticsKnockout MiceLeadMaintenanceMass Spectrum AnalysisMeasuresMediatingMetabolicMethodsModificationMusMutationNADPNatural regenerationNuclearOxidation-ReductionOxidative StressOxidesPathogenesisPathway interactionsPeripheralPermeabilityPlayPost-Translational Protein ProcessingProteinsRadialReactionRecoveryReduced GlutathioneRoleSenile CataractSpatial DistributionTechniquesTestingTracerVariantage relateddrug developmentexperimental studyfiber cellgap junction channelintercellular communicationinterestlenslens gap junctionlens transparencyoxidative damagepreventreal-time imagessight restorationthioredoxin reductase
项目摘要
PROJECT SUMMARY
Intercellular communication mediated by Cx46 and Cx50 gap junction channels is
central to the transport of ions into the lens and to the maintenance of lens transparency.
Studies on KO mice and on Cx46 and Cx50 mutations have established that the absence of gap
junctional coupling leads to cataracts. The main focus of this proposal is to examine the role of
gap junction (GJ) channels in the development of age-related nuclear cataracts. A key factor
that influences nuclear cataract formation is the abrupt age-dependent decline in the levels of
reduced glutathione (GSH) in the lens nucleus. This reduction in GSH levels is not observed in
the outer cortex and therefore has been attributed to the formation of a barrier to the diffusion of
GSH that develops with age. We have used electrophysiological techniques to show that that
Cx46 and Cx50 channels are permeable to GSH. Additional studies indicated that GSH is likely
to diffuse via Cx46 GJs from the cells in the outer cortex, where the anti-oxidant is synthesized,
to the metabolically quiescent cells in the lens nucleus. In this proposal, we will examine the role
of GJ channels in: (1) the establishment of a reducing environment in the lens nucleus, and (2)
mediating the shift to an oxidized environment that occurs with aging. We will use imaging and
mass spectrometry methods to directly measure the variation in the glutathione redox potential
from the lens periphery to the center in the intact lens. In Aim 1, we will assess the influence of
coupling levels on the spatial profile of glutathione redox potential in the intact lens. In Aim 2, we
will determine the permeability of gap junctions to other metabolites known to be essential for
the overall redox state of cells deep in the lens. In Aim 3, we will examine the relationship
between GJ channel functionality and changes in the glutathione redox potential that occur with
age. Specifically, we will determine whether post-translational modifications to Cx46 and Cx50
accumulate with age, leading to a reduction in GJ coupling, and ultimately to the development of
the barrier to GSH diffusion. These studies thus make a direct contribution to the understanding
of the mechanisms underlying the formation of ARN cataracts, and will serve to further highlight
the key role of GJ channels in maintenance of lens transparency.
项目摘要
由Cx46和Cx50间隙连接通道介导的细胞间通讯
这对于将离子输送到透镜中以及保持透镜的透明度至关重要。
对KO小鼠以及Cx46和Cx50突变的研究已经确定,
连接偶联导致白内障。本建议的主要重点是审查
缝隙连接(GJ)通道在年龄相关性核性白内障的发展。一个关键因素
影响核性白内障形成的因素是,
透镜核中的还原型谷胱甘肽(GSH)。GSH水平的这种降低在
外皮层,因此已被归因于形成一个屏障的扩散,
GSH随着年龄的增长而增加。我们已经用电生理技术证明,
Cx46和Cx50通道对GSH是可渗透的。进一步的研究表明,GSH可能是
通过Cx46 GJ从合成抗氧化剂的外皮层细胞扩散,
到透镜核中代谢静止的细胞。在本提案中,我们将研究
GJ通道在:(1)在透镜核中建立还原环境,和(2)
介导随着老化而发生的向氧化环境的转变。我们将使用成像技术,
直接测量谷胱甘肽氧化还原电位变化的质谱法
在完整的透镜中从透镜周边到中心。在目标1中,我们将评估
耦合水平对完整透镜中谷胱甘肽氧化还原电位的空间分布的影响。在目标2中,
将决定缝隙连接对其他代谢物的渗透性,这些代谢物是
透镜深处细胞的整体氧化还原状态。在目标3中,我们将研究
GJ通道功能和谷胱甘肽氧化还原电位的变化之间的关系,
年龄具体来说,我们将确定Cx46和Cx50的翻译后修饰是否
随着年龄的增长而积累,导致GJ耦合减少,并最终导致
GSH扩散的障碍。因此,这些研究直接有助于理解
ARN白内障形成的机制,并将进一步强调
GJ通道在保持透镜透明度中的关键作用。
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Age exacerbates the effect of myopia on retinal capillaries and string vessels.
- DOI:10.3389/fmed.2023.1112396
- 发表时间:2023
- 期刊:
- 影响因子:3.9
- 作者:
- 通讯作者:
Gap Junctional Coupling Between Retinal Astrocytes Exacerbates Neuronal Damage in Ischemia-Reperfusion Injury.
视网膜星形胶质细胞之间的间隙连接耦合加剧了缺血再灌注损伤中的神经元损伤。
- DOI:10.1167/iovs.62.14.27
- 发表时间:2021-11-01
- 期刊:
- 影响因子:4.4
- 作者:Toychiev AH;Batsuuri K;Srinivas M
- 通讯作者:Srinivas M
Myopia Alters the Structural Organization of the Retinal Vasculature, GFAP-Positive Glia, and Ganglion Cell Layer Thickness.
- DOI:10.3390/ijms23116202
- 发表时间:2022-05-31
- 期刊:
- 影响因子:5.6
- 作者:Lin, Carol;Toychiev, Abduqodir;Ablordeppey, Reynolds;Slavi, Nefeli;Srinivas, Miduturu;Benavente-Perez, Alexandra
- 通讯作者:Benavente-Perez, Alexandra
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Miduturu Srinivas其他文献
Miduturu Srinivas的其他文献
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{{ truncateString('Miduturu Srinivas', 18)}}的其他基金
Pharmacology of Connexin Channels: Structure-Activity Studies.
连接蛋白通道的药理学:结构-活性研究。
- 批准号:
7845504 - 财政年份:2009
- 资助金额:
$ 33.79万 - 项目类别:
Block of Lens and Neuronal Gap Junctions by Quinine
奎宁阻断晶状体和神经元间隙连接
- 批准号:
7122353 - 财政年份:2002
- 资助金额:
$ 33.79万 - 项目类别:
Block of Lens and Neuronal Gap Junctions by Quinine
奎宁阻断晶状体和神经元间隙连接
- 批准号:
6620670 - 财政年份:2002
- 资助金额:
$ 33.79万 - 项目类别:
Block of Lens and Neuronal Gap Junctions by Quinine
奎宁阻断晶状体和神经元间隙连接
- 批准号:
6983668 - 财政年份:2002
- 资助金额:
$ 33.79万 - 项目类别:
Block of Lens and Neuronal Gap Junctions by Quinine
奎宁阻断晶状体和神经元间隙连接
- 批准号:
6698790 - 财政年份:2002
- 资助金额:
$ 33.79万 - 项目类别:
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