Pilot Studies of the Effect of Aging on Mucociliary Clearance

衰老对粘液纤毛清除影响的初步研究

基本信息

项目摘要

DESCRIPTION (provided by applicant): Respiratory tract infections are a major cause of morbidity and mortality in the elderly population. In this population, pneumonia is the leading cause of death due to infectious disease, and the incidence of community-acquired pneumonia increases with every decade of life. One of the most important innate defense mechanisms against respiratory infections is the mucociliary clearance (MCC) system. Individuals with genetic defects in MCC suffer from chronic pulmonary infections, demonstrating the importance of MCC to host defense. Importantly, there is good evidence to suggest that MCC declines with age. Therefore it is likely that a reduced rate of MCC in the elderly, increases their susceptibiliy to respiratory infections. However, none of the studies reported to date has identified the mechanism(s) responsible for the reduced rate of MCC in older subjects, nor have they explored the effectiveness of treatments to improve MCC. Surprisingly, there have been no studies of the effect of aging on MCC in a mouse model. The lack of an established mouse model is a significant barrier, both to studies of the mechanisms responsible for the reduced rate of MCC in the elderly and to the development and testing of therapeutics designed to improve MCC in this population. Therefore the goals of this proposal are to 1) accurately assess the effect of aging on MCC in an established mouse model of aging, and 2) to examine the effect of aging on the key components of MCC to begin to identify the mechanisms responsible for the decreased rate of MCC in older subjects. Specific aim 1. To test the hypothesis that MCC is reduced in aged mice. Mucociliary clearance will be measured in the trachea and nasopharynx of 3, 6, 12, and 24 month old C57BL/6 mice by tracking the movement of endogenous mucus particles or instilled fluorescent beads. Specific aim 2. To examine the effect of age on individual components of the MCC. 2a) To test the hypothesis that aged mice exhibit defects in the ciliary component of MCC. Ciliary beat frequency (CBF) will be measured by video microscopy in the trachea and nasal cavity of 3, 6, 12, and 24 month old mice. The number of ciliated cells will be determined by histology, and the incidence of axonemal structural defects will be quantified by electron microscopy. 2b) To test the hypothesis that aged mice exhibit defects in the mucus component of MCC. The number of mucous cells in the nasal cavity and trachea will be determined by histology in samples from mice of different ages. The amount of secreted and total airway mucin in the lung will be quantified by agarose gel electrophoresis and Western blotting. 2c) To test the hypothesis that aged mice exhibit defects in the regulation of ion transport. The ion transport properties of the upper and lower airways wil be determined, as these are reflective of the hydration status of the ASL. Tissue samples from mice 3, 6, 12, and 24 months old will be studied in Ussing chambers. PUBLIC HEALTH RELEVANCE: The long-term goal of this research is to understand the cause of reduced mucociliary clearance and the high incidence of respiratory infections (pneumonia) in the elderly population, and to develop effective treatments to improve mucociliary clearance and prevent respiratory disease. In these pilot studies, mucociliary clearance will be measured in young and old mice to determine if mice can be used as a model for studies of mucociliary clearance in humans. Additional studies will investigate some of the possible mechanisms that may contribute to the reduced mucociliary clearance and increased respiratory infections in the elderly.
描述(由申请方提供):呼吸道感染是老年人群发病和死亡的主要原因。在这一人群中,肺炎是传染病导致死亡的主要原因,社区获得性肺炎的发病率随着年龄的增长而增加。对抗呼吸道感染的最重要的先天防御机制之一是粘膜纤毛清除(MCC)系统。具有MCC遗传缺陷的个体患有慢性肺部感染,表明MCC对宿主防御的重要性。重要的是,有很好的证据表明MCC随着年龄的增长而下降。因此,老年人MCC发生率的降低可能会增加他们对呼吸道感染的易感性。然而,迄今为止报告的研究均未确定老年受试者中MCC发生率降低的机制,也未探索治疗改善MCC的有效性。令人惊讶的是,在小鼠模型中没有研究衰老对MCC的影响。缺乏已建立的小鼠模型是一个重大障碍,无论是对老年人MCC发病率降低机制的研究,还是对旨在改善该人群MCC的治疗方法的开发和测试。因此,本提案的目标是:1)在已建立的衰老小鼠模型中准确评估衰老对MCC的影响,以及2)检查衰老对MCC关键组分的影响,以开始确定老年受试者中MCC发生率降低的机制。具体目标1.验证老年小鼠MCC减少的假设。通过跟踪内源性粘液颗粒或滴注荧光珠的运动,测量3、6、12和24月龄C57 BL/6小鼠气管和鼻咽中的粘液纤毛清除率。具体目标2。检查年龄对MCC单个组分的影响。2a)检验老年小鼠表现出MCC纤毛组分缺陷的假设。将通过视频显微镜测量3、6、12和24月龄小鼠气管和鼻腔中的纤毛搏动频率(CBF)。纤毛细胞的数量将通过组织学确定,轴丝结构缺陷的发生率将通过电子显微镜定量。2b)检验老年小鼠表现出MCC粘液组分缺陷的假设。将通过组织学方法测定不同年龄小鼠样品中鼻腔和气管中粘液细胞的数量。通过琼脂糖凝胶电泳和蛋白质印迹定量肺中分泌的和总气道粘蛋白的量。2c)验证老龄小鼠在离子转运调节方面表现出缺陷的假设。将确定上气道和下气道的离子转运特性,因为这些特性反映了ASL的水合状态。将在Ussing室中研究3、6、12和24月龄小鼠的组织样本。 公共卫生关系:本研究的长期目标是了解老年人群中粘膜纤毛清除率降低和呼吸道感染(肺炎)高发的原因,并开发有效的治疗方法来改善粘膜纤毛清除率和预防呼吸道疾病。在这些初步研究中,将在年轻和年老小鼠中测量粘膜纤毛清除率,以确定小鼠是否可用作人体粘膜纤毛清除率研究的模型。其他研究将调查一些可能的机制,可能有助于减少老年人的粘膜纤毛清除和呼吸道感染增加。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

LAWRENCE E OSTROWSKI其他文献

LAWRENCE E OSTROWSKI的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('LAWRENCE E OSTROWSKI', 18)}}的其他基金

Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia
原发性纤毛运动障碍新突变基因的功能研究
  • 批准号:
    8721483
  • 财政年份:
    2013
  • 资助金额:
    $ 7.6万
  • 项目类别:
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia
原发性纤毛运动障碍新突变基因的功能研究
  • 批准号:
    8480072
  • 财政年份:
    2013
  • 资助金额:
    $ 7.6万
  • 项目类别:
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia
原发性纤毛运动障碍新突变基因的功能研究
  • 批准号:
    8829895
  • 财政年份:
    2013
  • 资助金额:
    $ 7.6万
  • 项目类别:
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype
原发性纤毛运动障碍 II 中新突变基因的功能研究:基因型到表型
  • 批准号:
    10363650
  • 财政年份:
    2013
  • 资助金额:
    $ 7.6万
  • 项目类别:
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype
原发性纤毛运动障碍 II 中新突变基因的功能研究:基因型到表型
  • 批准号:
    10570977
  • 财政年份:
    2013
  • 资助金额:
    $ 7.6万
  • 项目类别:
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype
原发性纤毛运动障碍 II 中新突变基因的功能研究:基因型到表型
  • 批准号:
    9887916
  • 财政年份:
    2013
  • 资助金额:
    $ 7.6万
  • 项目类别:
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia
原发性纤毛运动障碍新突变基因的功能研究
  • 批准号:
    9242066
  • 财政年份:
    2013
  • 资助金额:
    $ 7.6万
  • 项目类别:
Pilot Studies of the Effect of Aging on Mucociliary Clearance
衰老对粘液纤毛清除影响的初步研究
  • 批准号:
    8513866
  • 财政年份:
    2012
  • 资助金额:
    $ 7.6万
  • 项目类别:
Pilot Studies of Gene Therapy for Primary Ciliary Dyskinesia
原发性纤毛运动障碍基因治疗的初步研究
  • 批准号:
    7935357
  • 财政年份:
    2009
  • 资助金额:
    $ 7.6万
  • 项目类别:
Pilot Studies of Gene Therapy for Primary Ciliary Dyskinesia
原发性纤毛运动障碍基因治疗的初步研究
  • 批准号:
    7829389
  • 财政年份:
    2009
  • 资助金额:
    $ 7.6万
  • 项目类别:

相似国自然基金

靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
  • 批准号:
    JCZRQN202500010
  • 批准年份:
    2025
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
  • 批准号:
    2025JJ70209
  • 批准年份:
    2025
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
  • 批准年份:
    2024
  • 资助金额:
    0 万元
  • 项目类别:
    面上项目
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
  • 批准号:
    2023JJ50274
  • 批准年份:
    2023
  • 资助金额:
    0.0 万元
  • 项目类别:
    省市级项目
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
  • 批准号:
  • 批准年份:
    2022
  • 资助金额:
    33 万元
  • 项目类别:
    地区科学基金项目
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
  • 批准号:
  • 批准年份:
    2022
  • 资助金额:
    10.0 万元
  • 项目类别:
    省市级项目
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
  • 批准号:
    81973577
  • 批准年份:
    2019
  • 资助金额:
    55.0 万元
  • 项目类别:
    面上项目
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
  • 批准号:
    81602908
  • 批准年份:
    2016
  • 资助金额:
    18.0 万元
  • 项目类别:
    青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
  • 批准号:
    81501928
  • 批准年份:
    2015
  • 资助金额:
    18.0 万元
  • 项目类别:
    青年科学基金项目

相似海外基金

PROTEMO: Emotional Dynamics Of Protective Policies In An Age Of Insecurity
PROTEMO:不安全时代保护政​​策的情绪动态
  • 批准号:
    10108433
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    EU-Funded
The role of dietary and blood proteins in the prevention and development of major age-related diseases
膳食和血液蛋白在预防和发展主要与年龄相关的疾病中的作用
  • 批准号:
    MR/X032809/1
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Fellowship
Atomic Anxiety in the New Nuclear Age: How Can Arms Control and Disarmament Reduce the Risk of Nuclear War?
新核时代的原子焦虑:军控与裁军如何降低核战争风险?
  • 批准号:
    MR/X034690/1
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Fellowship
Collaborative Research: Resolving the LGM ventilation age conundrum: New radiocarbon records from high sedimentation rate sites in the deep western Pacific
合作研究:解决LGM通风年龄难题:西太平洋深部高沉降率地点的新放射性碳记录
  • 批准号:
    2341426
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Continuing Grant
Collaborative Research: Resolving the LGM ventilation age conundrum: New radiocarbon records from high sedimentation rate sites in the deep western Pacific
合作研究:解决LGM通风年龄难题:西太平洋深部高沉降率地点的新放射性碳记录
  • 批准号:
    2341424
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Continuing Grant
Doctoral Dissertation Research: Effects of age of acquisition in emerging sign languages
博士论文研究:新兴手语习得年龄的影响
  • 批准号:
    2335955
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Standard Grant
The economics of (mis)information in the age of social media
社交媒体时代(错误)信息的经济学
  • 批准号:
    DP240103257
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Discovery Projects
How age & sex impact the transcriptional control of mammalian muscle growth
你多大
  • 批准号:
    DP240100408
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Discovery Projects
Supporting teachers and teaching in the age of Artificial Intelligence
支持人工智能时代的教师和教学
  • 批准号:
    DP240100111
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Discovery Projects
Enhancing Wahkohtowin (Kinship beyond the immediate family) Community-based models of care to reach and support Indigenous and racialized women of reproductive age and pregnant women in Canada for the prevention of congenital syphilis
加强 Wahkohtowin(直系亲属以外的亲属关系)以社区为基础的护理模式,以接触和支持加拿大的土著和种族育龄妇女以及孕妇,预防先天梅毒
  • 批准号:
    502786
  • 财政年份:
    2024
  • 资助金额:
    $ 7.6万
  • 项目类别:
    Directed Grant
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了