An in vitro system for the study of epithelial bicarbonate secretion

用于研究上皮碳酸氢盐分泌的体外系统

基本信息

项目摘要

DESCRIPTION (provided by applicant): Bicarbonate secretion plays an essential role in the physiological functioning of the duodenum, airway, pancreas, liver, male reproductive system, and kidney. Impairment of bicarbonate secretion, such as is manifest in the disease cystic fibrosis, can produce severe pathology in some or all of these organs. The mechanism of bicarbonate secretion is still not fully understood, despite decades of intensive study. Part of the problem is the methodology inherent in its study, which can involve intestinal, pancreatic duct, and renal tubule perfusion, and indirect methods, usually in live animals or in intact tissue. All of these methods suffer from excessive expense, cumbersome and time-consuming procedures, the use of laboratory animals which entails considerable expense and near- prohibitive regulatory requirements, and heterogeneity and lack of viability of the tissues studied. A bicarbonate-secreting in vitro system, although overcoming most of these obstacles, has not yet been developed. We propose to develop a bicarbonate secreting system based on commonly studied epithelial cell lines that have attributes similar to bicarbonate secreting intact epithelia and are thus likely to have measurable bicarbonate secretion. Our methodology includes culturing Caco-2 intestinal cells, or alternatively MDCK or other epithelial-derived cultured cells, on semi-permeable supports that can then be mounted in a perfusion chamber that enables the measurement of bicarbonate secretion, in addition to ratiometric measurement of intracellular pH, and short-circuit current across the monolayer. In this fashion, we plan to generate data that will enable us to test several key hypotheses. PUBLIC HEALTH RELEVANCE: Bicarbonate (baking soda) is secreted by the intestine in order to neutralize acid that is secreted by the stomach. Bicarbonate is also secreted by other important organs such as the pancreas, liver, lung, and male reproductive system. Disorders of bicarbonate secretion, as are found in the disease cystic fibrosis, can cause severe problems such as lung disease, pancreatitis, intestinal obstruction, and male infertility. Study of the mechanism of bicarbonate secretion has been hampered by the lack of a suitable model other than the use of live animals. We propose a cell-culture-based system suitable for the study of bicarbonate secretion that will help us and other investigators study how bicarbonate is secreted. With this knowledge, we hope to further understand why problems with bicarbonate secretion can lead to such sever diseases such as cystic fibrosis.
描述(由申请方提供):双歧杆菌分泌在十二指肠、气道、胰腺、肝脏、男性生殖系统和肾脏的生理功能中起重要作用。碳酸氢盐分泌的损害,例如在囊性纤维化疾病中表现的,可以在这些器官中的一些或全部中产生严重的病理。碳酸氢盐分泌的机制仍然没有完全理解,尽管几十年的深入研究。部分问题在于其研究中固有的方法学,包括肠、胰管和肾小管灌注,以及间接方法,通常在活体动物或完整组织中进行。所有这些方法都存在费用过高、程序繁琐和耗时、使用实验室动物(这需要相当大的费用和近乎禁止的监管要求)以及所研究组织的异质性和缺乏活力的问题。尽管克服了这些障碍中的大多数,但尚未开发出分泌碳酸氢盐的体外系统。我们建议基于通常研究的上皮细胞系开发碳酸氢盐分泌系统,所述上皮细胞系具有与碳酸氢盐分泌完整上皮相似的属性,因此可能具有可测量的碳酸氢盐分泌。我们的方法包括在半渗透性支持物上培养Caco-2肠细胞,或者MDCK或其他上皮来源的培养细胞,然后将其安装在灌注室中,除了细胞内pH值的比率测量外,还可以测量碳酸氢盐分泌和单层短路电流。以这种方式,我们计划生成数据,使我们能够测试几个关键假设。公共卫生相关性:Biclitazone(小苏打)是由肠道分泌的,以中和胃分泌的酸。其他重要器官如胰腺、肝脏、肺和男性生殖系统也会分泌Biclidine。在囊性纤维化疾病中发现的碳酸氢盐分泌障碍可导致严重的问题,如肺部疾病、胰腺炎、肠梗阻和男性不育。碳酸氢盐分泌机制的研究由于缺乏合适的模型而受到阻碍,而不是使用活动物。我们提出了一种适合于研究碳酸氢盐分泌的基于细胞培养的系统,这将有助于我们和其他研究人员研究碳酸氢盐是如何分泌的。有了这些知识,我们希望进一步了解为什么碳酸氢盐分泌问题会导致囊性纤维化等严重疾病。

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 }}

Jonathan D. Kaunitz其他文献

The GI Effects of GLP-1 – The Genesis of Longstanding Progress
  • DOI:
    10.1007/s10620-022-07520-w
  • 发表时间:
    2022-05-30
  • 期刊:
  • 影响因子:
    2.500
  • 作者:
    Jonathan D. Kaunitz
  • 通讯作者:
    Jonathan D. Kaunitz
Mo1171 - Functional Localization of Ffa2 to the Basolateral Membrane of Enterochromaffin Cells in Rat and Mouse Duodenum
  • DOI:
    10.1016/s0016-5085(18)32452-1
  • 发表时间:
    2018-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    Yasutada Akiba;Takeshi Takajo;Jonathan D. Kaunitz
  • 通讯作者:
    Jonathan D. Kaunitz
34 Luminal Acetate Stimulates Duodenal HCO<sub>3</sub><sup>−</sup> Secretion via GLP-2 Release, 5-HT<sub>4</sub> Receptor Activation, the Prostaglandin and Capsaicin Pathways, and Absorptive Transporters
  • DOI:
    10.1016/s0016-5085(13)60030-x
  • 发表时间:
    2013-05-01
  • 期刊:
  • 影响因子:
  • 作者:
    Izumi Kaji;Yasutada Akiba;Paul H. Guth;Eli Engel;Jonathan D. Kaunitz
  • 通讯作者:
    Jonathan D. Kaunitz
Importance of cellular base loading in duodenal mucosal defence
  • DOI:
    10.1016/s0016-5085(00)82998-4
  • 发表时间:
    2000-04-01
  • 期刊:
  • 影响因子:
  • 作者:
    Yasutada Akiba;Paul H. Guth;Eli Engel;Jonathan D. Kaunitz
  • 通讯作者:
    Jonathan D. Kaunitz
Welcome Associate Editors Andrew Stewart Day and Hiromu Suzuki
欢迎副编辑安德鲁·斯图尔特·戴和铃木弘
  • DOI:
    10.1007/s10620-020-06778-2
  • 发表时间:
    2021-01-11
  • 期刊:
  • 影响因子:
    2.500
  • 作者:
    Jonathan D. Kaunitz
  • 通讯作者:
    Jonathan D. Kaunitz

Jonathan D. Kaunitz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('Jonathan D. Kaunitz', 18)}}的其他基金

Luminal factors affecting duodenal protection and chemosensing
影响十二指肠保护和化学传感的管腔因素
  • 批准号:
    8333742
  • 财政年份:
    2012
  • 资助金额:
    $ 15.58万
  • 项目类别:
Luminal factors affecting duodenal protection and chemosensing
影响十二指肠保护和化学传感的管腔因素
  • 批准号:
    8803262
  • 财政年份:
    2012
  • 资助金额:
    $ 15.58万
  • 项目类别:
Luminal factors affecting duodenal protection and chemosensing
影响十二指肠保护和化学传感的管腔因素
  • 批准号:
    8698268
  • 财政年份:
    2012
  • 资助金额:
    $ 15.58万
  • 项目类别:
Luminal Factors Affecting Duodenal Protection and Chemosensing
影响十二指肠保护和化学传感的管腔因素
  • 批准号:
    10700480
  • 财政年份:
    2012
  • 资助金额:
    $ 15.58万
  • 项目类别:
Luminal factors affecting duodenal protection and chemosensing
影响十二指肠保护和化学传感的管腔因素
  • 批准号:
    8517440
  • 财政年份:
    2012
  • 资助金额:
    $ 15.58万
  • 项目类别:
An in vitro system for the study of epithelial bicarbonate secretion
用于研究上皮碳酸氢盐分泌的体外系统
  • 批准号:
    7743851
  • 财政年份:
    2009
  • 资助金额:
    $ 15.58万
  • 项目类别:
DUODENAL MUCOSAL DEFENSE MECHANISM
十二指肠粘膜防御机制
  • 批准号:
    6177886
  • 财政年份:
    1999
  • 资助金额:
    $ 15.58万
  • 项目类别:
Duodenal Muscosal Defense Mechanisms
十二指肠粘膜防御机制
  • 批准号:
    7017701
  • 财政年份:
    1999
  • 资助金额:
    $ 15.58万
  • 项目类别:
Duodenal Mucosal Defense Mechanisms
十二指肠粘膜防御机制
  • 批准号:
    7356225
  • 财政年份:
    1999
  • 资助金额:
    $ 15.58万
  • 项目类别:
Duodenal Muscosal Defense Mechanisms
十二指肠粘膜防御机制
  • 批准号:
    6850669
  • 财政年份:
    1999
  • 资助金额:
    $ 15.58万
  • 项目类别:

相似海外基金

Rational design of rapidly translatable, highly antigenic and novel recombinant immunogens to address deficiencies of current snakebite treatments
合理设计可快速翻译、高抗原性和新型重组免疫原,以解决当前蛇咬伤治疗的缺陷
  • 批准号:
    MR/S03398X/2
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    Fellowship
Re-thinking drug nanocrystals as highly loaded vectors to address key unmet therapeutic challenges
重新思考药物纳米晶体作为高负载载体以解决关键的未满足的治疗挑战
  • 批准号:
    EP/Y001486/1
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    Research Grant
CAREER: FEAST (Food Ecosystems And circularity for Sustainable Transformation) framework to address Hidden Hunger
职业:FEAST(食品生态系统和可持续转型循环)框架解决隐性饥饿
  • 批准号:
    2338423
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    Continuing Grant
Metrology to address ion suppression in multimodal mass spectrometry imaging with application in oncology
计量学解决多模态质谱成像中的离子抑制问题及其在肿瘤学中的应用
  • 批准号:
    MR/X03657X/1
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    Fellowship
CRII: SHF: A Novel Address Translation Architecture for Virtualized Clouds
CRII:SHF:一种用于虚拟化云的新型地址转换架构
  • 批准号:
    2348066
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    Standard Grant
BIORETS: Convergence Research Experiences for Teachers in Synthetic and Systems Biology to Address Challenges in Food, Health, Energy, and Environment
BIORETS:合成和系统生物学教师的融合研究经验,以应对食品、健康、能源和环境方面的挑战
  • 批准号:
    2341402
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    Standard Grant
The Abundance Project: Enhancing Cultural & Green Inclusion in Social Prescribing in Southwest London to Address Ethnic Inequalities in Mental Health
丰富项目:增强文化
  • 批准号:
    AH/Z505481/1
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    Research Grant
ERAMET - Ecosystem for rapid adoption of modelling and simulation METhods to address regulatory needs in the development of orphan and paediatric medicines
ERAMET - 快速采用建模和模拟方法的生态系统,以满足孤儿药和儿科药物开发中的监管需求
  • 批准号:
    10107647
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    EU-Funded
Ecosystem for rapid adoption of modelling and simulation METhods to address regulatory needs in the development of orphan and paediatric medicines
快速采用建模和模拟方法的生态系统,以满足孤儿药和儿科药物开发中的监管需求
  • 批准号:
    10106221
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    EU-Funded
Recite: Building Research by Communities to Address Inequities through Expression
背诵:社区开展研究,通过表达解决不平等问题
  • 批准号:
    AH/Z505341/1
  • 财政年份:
    2024
  • 资助金额:
    $ 15.58万
  • 项目类别:
    Research Grant
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了