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Mimicking Vascular Endothelial Cell In Vivo Environment in Cell Culture

Mimicking Vascular Endothelial Cell In Vivo Environment in Cell Culture
在细胞培养中模拟体内环境中的血管内皮细胞
批准号:
RGPIN-2017-06336
负责人:
Cepinskas, Gediminas
金额:
$1.89万
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2018
资助国家:
加拿大
项目状态:
已结题
起止时间:
2018-01-01 至 2019-12-31

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中文摘要
翻译
导言:实验血管生物学领域的科学家一直面临着两大挑战:1)将多种机械力(如剪应力、循环应变和静水压力)整合到使用体外细胞培养(如血管内皮细胞)的实验系统(S)中;2)大多数细胞培养是在环境氧气(即21%O2)中生长的事实,而不是大多数器官/组织中看到的5%O2的生理水平。关于前者,相对于剪切应力和循环应变的研究,静水压力对EC响应的影响/机制的研究受到的关注要少得多。静水压力(如静水压力的增加),曾经被认为是一种纯粹的“机械成分”,因此是一种相对良性的病理生理状况,最近被认为是一种潜在的刺激,诱导机械信号传递。有限的研究结果(包括我们自己的研究结果)表明,静水压力的增加会诱导复杂和高度敏感的细胞反应,因此,可能在微循环的调节中发挥关键作用。静水压力引起的血管内皮细胞生理/病理生理反应变化的机制尚不清楚。*细胞生物学家面临的另一个主要挑战是大多数细胞在体外实验中生长和使用的条件。通常的做法是在环境氧气(即21%O2)中培养细胞。然而,大多数人体细胞暴露在大约5%的氧气中,从而使普遍接受的细胞生长和实验条件(例如,室内空气;21%O2)严重地“高氧”和非生理性。*研究方法:本研究计划的主要目标是研究血管内皮细胞对静水压力的反应(例如,分子信号和功能后果),并进一步发展一种新的实验模型,以便在体外研究生理O2水平下静水压力的影响/机制。*本研究将使用代表各种血管床的原代人血管内皮细胞培养(例如,来自脑、肺、皮肤的微血管内皮细胞),这些细胞将在5%O2和静水压力(0-30 mm Hg)的条件下培养并用于实验,采用最先进的微灌流和细胞共培养方法。细胞功能/功能障碍的各个方面(例如,氧化剂、细胞因子的产生、细胞骨架的重排、通透性和黏附前表型的变化等)。将会被评估。*期望:这项研究计划将允许开发一种新的体外实验模型,接近模拟体内的生理/病理生理学条件。此外,它还将为培养至少三名硕士研究生提供良好的基础。
英文摘要
Introduction: Scientists in the field of experimental vascular biology are constantly confronting two major challenges: 1) integration of multiple mechanical forces (e.g. shear stress, cyclic strain, and hydrostatic pressure) into the experimental system(s) that employ in vitro cell cultures (e.g. vascular endothelial cells) and 2) the fact that most cell cultures are grown at the ambient O2 (i.e. 21% O2) as opposed to physiological levels of 5% O2 seen in most organs/tissues. ***In regard to the former, studying the effects/mechanisms of hydrostatic pressure on EC responses have received much less attention relative to studies of shear stress and cyclic strain. Hydrostatic pressure (e.g. increase in hydrostatic pressure), that once was considered a purely “mechanical component” and hence, a relatively benign pathophysiological condition, recently has been recognized as a potential stimulus inducing mechanosignaling. Limited research findings (including our own) indicate that increase in hydrostatic pressure induces complex and highly sensitive cellular responses, therefore, may play a critical role in regulation of the microcirculation. The mechanistic aspects of hydrostatic pressure-induced changes in vascular endothelial cell physiological/pathophysiological responses remain poorly understood.***The other major challenge for cell biologists is the conditions at which most of cells are grown and used in the in vitro experiments. The common practice is to culture the cells at the ambient O2 (i.e. 21% O2). However, most of the body's cells are exposed to approximately 5% O2, thus making commonly accepted conditions of cell growth and experimentation (e.g. room air; 21% O2) severely “hyperoxic” and unphysiological. ***Research Approach: The main goal of this research program is to investigate vascular endothelial cell responses (e.g. molecular signaling and functional consequences) to hydrostatic pressure and to further develop a new experimental model allowing investigating the effects/mechanisms of hydrostatic pressure in vitro under physiological O2 levels.***This study will use primary human vascular endothelial cell cultures representing various vascular beds (e.g. microvascular EC derived from brain, lung, skin) which will be cultured and used in the experiments under conditions of 5% O2 and hydrostatic pressure (0-30 mmHg) employing state-of-the-art microperfusion and cell co-culture approaches. Various aspects of cell function/dysfunction (e.g. production of oxidants, cytokines, rearrangement of cytoskeleton, changes in permeability and pro-adhesive phenotype, etc.) will be assessed. ***Expectations: This research program will allow to develop a new experimental model in vitro closely mimicking physiological/pathophysiological conditions in vivo. In addition, it will provide excellent grounds for training of at least three graduate (MSc) students.
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Mimicking Vascular Endothelial Cell In Vivo Environment in Cell Culture
  • 批准号:
    RGPIN-2017-06336
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.79万
  • 财政年份:
    2021
  • 负责人:
    Cepinskas, Gediminas
  • 依托单位:
Mimicking Vascular Endothelial Cell In Vivo Environment in Cell Culture
  • 批准号:
    RGPIN-2017-06336
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $1.89万
  • 财政年份:
    2020
  • 负责人:
    Cepinskas, Gediminas
  • 依托单位:
Mimicking Vascular Endothelial Cell In Vivo Environment in Cell Culture
  • 批准号:
    RGPIN-2017-06336
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $1.89万
  • 财政年份:
    2019
  • 负责人:
    Cepinskas, Gediminas
  • 依托单位:
Mimicking Vascular Endothelial Cell In Vivo Environment in Cell Culture
  • 批准号:
    RGPIN-2017-06336
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $1.89万
  • 财政年份:
    2017
  • 负责人:
    Cepinskas, Gediminas
  • 依托单位:
海外基金