3-Dimensional modeling of basal cell function in pseudostratified epithelia

假复层上皮基底细胞功能的三维建模

基本信息

批准号：
8327225
负责人：
SYLVIE BRETON
金额：
$ 55.82万
依托单位：
MASSACHUSETTS GENERAL HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-09-21 至 2014-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8327225
关键词：
3-Dimensional AQP9 gene Air Animal Model Animals Apical Asthma Basal Cell Behavior Biological Models Biology Blood Breathing Breeding Cell Line Cell physiology Cells Characteristics Chemicals Chronic Obstructive Airway Disease Clear Cell Color Communication Complex Crossbreeding Cyan Fluorescent Protein Cystic Fibrosis Data Dendritic Cells Development Diagnostic Disease Electrodes Epididymis Epithelial Cells Epithelium Female Fertility Future Genes Gland Goals Green Fluorescent Proteins Hormones Human ITGAX gene Image Individual Intercalated Cell Invaded Ion-Selective Electrodes Ions Kidney Knowledge Laboratories Larynx Laser Scanning Confocal Microscopy Life Liquid substance Lung Lung diseases Male Infertility Measures Microelectrodes Microscope Modeling Monitor Mus Nitric Oxide Olfactory Mucosa Organ Organism Pharmaceutical Preparations Play Production Property Prostate Proteins Pseudostratified Epithelium Research Research Proposals Role Sampling Scanning Sensory Side Stimulus Structure System Systems Biology Testis Therapeutic Intervention Three-Dimensional Imaging Tight Junctions Time Tissue Model Tissues Trachea Transgenic Mice Tube United States National Institutes of Health Upper respiratory tract Vas deferens structure Vision cell type in vivo innovation insight intercellular communication male miniaturize mouse model novel novel diagnostics novel strategies novel therapeutics pathogen programs promoter red fluorescent protein reproductive response sensor sperm cell time use tool water channel

项目摘要

DESCRIPTION (provided by applicant): A current paradigm in biology is that so-called basal cells, present in pseudostratified epithelia, are never in contact with the luminal side of an organ. In contrast to this dogma, we recently showed that these cells extend slender body projections that cross the tight-junction barrier to reach the lumen. This research proposal is driven by this paradigm-shifting discovery. We found that basal cells scan the luminal side of selected epithelia and modulate their function via crosstalk with other epithelial cells. We observed "apical-reaching" basal cells in several tissues of the male reproductive and upper respiratory tracts indicating that the luminal sampling property of basal cells is a generalized phenomenon. In this research program, we will examine the spatial, temporal and motional behavior of basal cells in vivo and we will characterize the intercellular communication networks between basal cells and adjacent cells. To do so, we will generate novel mice expressing the red fluorescent protein, mRaspberry, in basal cells exclusively. We will cross-breed these mice with current mice available in our laboratory, including CD11c-YFP mice that express the yellow fluorescent protein in dendritic cells, and B1-EGFP mice that express the green fluorescent protein EGFP in epididymal clear cells, non- ciliated cells of the lung, and kidney intercalated cells. This will generate a novel animal model in which several cell types will be imaged simultaneously, in live animals, using intravital multiphoton microscopes equipped with miniaturized objectives, and in which ionic and nitric oxide fluxes will be measured in real time using selective microelectrodes. We will focus on two epithelia, the epididymis, which is at the core of our research program, and the trachea. The epididymis, which connects the testis to the vas deferens, is involved in the maturation and storage of spermatozoa and, therefore, plays a crucial role in male fertility. The other target tissue of this application, the trachea, is constantly invaded by foreign allergenic and pathogenic substances, and provides a structural barrier between the airway and the body. We propose that basal cells are front-line sensors that probe luminal factors that regulate male fertility in the epididymis, and inhaled molecules in the trachea. A better understanding of the novel apical sensory role of basal cells and how they transmit their findings to adjacent cells will help define the pathophysiological mechanisms underlying male infertility, and diseases of the lung, including asthma, chronic obstructive pulmonary disease (COPD) and cystic fibrosis (CF). Monitoring and decoding intercellular conversations in the epididymis and trachea will, thus, promote innovative diagnostic and therapeutic interventions for the treatment of these diseases. In addition, this research program will have broader implications for our understanding of epithelia in general, as data generated here will provide unprecedented insights into the communication network established by complex tissues and on how it is perturbed in disease.

描述（由申请人提供）：生物学中当前的范例是，存在于假复层上皮中的所谓基底细胞从不与器官的管腔侧接触。与这种教条相反，我们最近发现这些细胞延伸出细长的身体突出物，穿过紧密连接屏障到达管腔。这项研究提案是由这一范式转变的发现推动的。我们发现基底细胞扫描选定上皮细胞的管腔侧并通过与其他上皮细胞的串扰来调节其功能。我们在男性生殖道和上呼吸道的几个组织中观察到“到达顶端”的基底细胞，表明基底细胞的管腔采样特性是一种普遍现象。在本研究项目中，我们将研究基底细胞在体内的空间、时间和运动行为，并表征基底细胞和相邻细胞之间的细胞间通讯网络。为此，我们将培育出仅在基底细胞中表达红色荧光蛋白 mRaspberry 的新型小鼠。我们将把这些小鼠与我们实验室现有的小鼠进行杂交，包括在树突状细胞中表达黄色荧光蛋白的 CD11c-YFP 小鼠，以及在附睾透明细胞、非纤毛细胞中表达绿色荧光蛋白 EGFP 的 B1-EGFP 小鼠。肺细胞和肾闰细胞。这将产生一种新颖的动物模型，其中使用配备微型物镜的活体多光子显微镜对活体动物中的多种细胞类型同时成像，并使用选择性微电极实时测量离子和一氧化氮通量。我们将重点关注两种上皮细胞：附睾（我们研究计划的核心）和气管。附睾连接睾丸和输精管，参与精子的成熟和储存，因此在男性生育能力中发挥着至关重要的作用。该应用的另一个目标组织是气管，不断受到外来过敏和致病物质的侵袭，并在气道和身体之间提供了结构屏障。我们认为基底细胞是探测附睾中调节男性生育能力的管腔因子和气管中吸入分子的前线传感器。更好地了解基底细胞的新的顶端感觉作用以及它们如何将其发现传递给邻近细胞将有助于确定男性不育和肺部疾病（包括哮喘、慢性阻塞性肺病（COPD）和囊性纤维化）的病理生理机制（CF）。因此，监测和解码附睾和气管中的细胞间对话将促进治疗这些疾病的创新诊断和治疗干预措施。此外，该研究计划将对我们对上皮细胞的总体理解产生更广泛的影响，因为这里生成的数据将为复杂组织建立的通信网络及其在疾病中如何受到干扰提供前所未有的见解。