Cell Physiology Core

细胞生理学核心

基本信息

  • 批准号:
    10200121
  • 负责人:
  • 金额:
    $ 31.48万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2014
  • 资助国家:
    美国
  • 起止时间:
    2014-08-01 至 2024-05-31
  • 项目状态:
    已结题

项目摘要

CORE C PROJECT SUMMARY Pannexin 1 (Panx1) forms plasma membrane ion channels that release important intercellular signalling molecules, specifically ATP and UTP, under pathological and physiological conditions; the channels also support uptake of various fluorescent dyes that have traditionally been used to mark apoptotic cells (e.g., YO-PRO-1, TO-PRO-3). In this PPG application, novel mouse models are employed to ascertain contributions of Panx1- mediated ATP/UTP release, (and other metabolite release, when needed) to various aspects of cardiometabolic diseases, and to understand corresponding mechanisms of Panx1 channel activation. Cell Physiology Core centralizes the functional analysis of Pannexin channels by absorbing, optimizing and standardizing the key assays of universal significance to all four projects. These include: (1) Analysis of Panx1 channel function in primary cells by electrophysiology and dye uptake assays and; (2) Electrophysiological characterization of novel small molecule modulators of Pannexin channels. Similarly, the core also takes the initiative in the development of innovative tools and methods that can provide a clear technical edge to the entire research program. This includes generation of novel Panx1 variants and gene-edited mouse lines, generated by CRISPR/Cas9 technology. In executing these centralized goals, often of salience to the entire research program, the core recognizes the paramount importance of data quality and reproducibility. For the vertical and horizontal integration proposed in this PPG, this core sits at the interface between cellular and systems levels of analysis of Panx1 function.
Core c项目总结

项目成果

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专利数量(0)

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BIMAL N. DESAI其他文献

BIMAL N. DESAI的其他文献

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{{ truncateString('BIMAL N. DESAI', 18)}}的其他基金

Mitochondrial Calcium Signaling in Cell Intrinsic Immunity
细胞内在免疫中的线粒体钙信号传导
  • 批准号:
    10620267
  • 财政年份:
    2021
  • 资助金额:
    $ 31.48万
  • 项目类别:
Mitochondrial Calcium Signaling in Cell Intrinsic Immunity
细胞内在免疫中的线粒体钙信号传导
  • 批准号:
    10297192
  • 财政年份:
    2021
  • 资助金额:
    $ 31.48万
  • 项目类别:
Mitochondrial Calcium Signaling in Cell Intrinsic Immunity
细胞内在免疫中的线粒体钙信号传导
  • 批准号:
    10424585
  • 财政年份:
    2021
  • 资助金额:
    $ 31.48万
  • 项目类别:
TRPM7 at the Crossroads of Tissue Homeostasis and inflammation
TRPM7 处于组织稳态和炎症的十字路口
  • 批准号:
    10409807
  • 财政年份:
    2016
  • 资助金额:
    $ 31.48万
  • 项目类别:
The regulation and function of TRPM7 in inflammation
TRPM7在炎症中的调控及功能
  • 批准号:
    9198955
  • 财政年份:
    2016
  • 资助金额:
    $ 31.48万
  • 项目类别:
TRPM7 at the Crossroads of Tissue Homeostasis and inflammation
TRPM7 处于组织稳态和炎症的十字路口
  • 批准号:
    10210717
  • 财政年份:
    2016
  • 资助金额:
    $ 31.48万
  • 项目类别:
TRPM7 at the Crossroads of Tissue Homeostasis and inflammation
TRPM7 处于组织稳态和炎症的十字路口
  • 批准号:
    10569632
  • 财政年份:
    2016
  • 资助金额:
    $ 31.48万
  • 项目类别:
The regulation and function of TRPM7 in inflammation
TRPM7在炎症中的调控及功能
  • 批准号:
    9028940
  • 财政年份:
    2016
  • 资助金额:
    $ 31.48万
  • 项目类别:
Cell Physiology Core
细胞生理学核心
  • 批准号:
    10407612
  • 财政年份:
    2014
  • 资助金额:
    $ 31.48万
  • 项目类别:
Cell Physiology Core
细胞生理学核心
  • 批准号:
    10625323
  • 财政年份:
    2014
  • 资助金额:
    $ 31.48万
  • 项目类别:

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细胞中激活凋亡半胱天冬酶的生/死决策的机制
  • 批准号:
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Caspase-3在神经发育中的非凋亡功能
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    2023
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    $ 31.48万
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凋亡供体白细胞促进肾移植耐受
  • 批准号:
    10622209
  • 财政年份:
    2023
  • 资助金额:
    $ 31.48万
  • 项目类别:
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用于治疗细胞因子风暴的模拟凋亡细胞抗炎聚合物的设计
  • 批准号:
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确定线粒体基质定位的 MCL-1 非凋亡功能背后的机制
  • 批准号:
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  • 财政年份:
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  • 资助金额:
    $ 31.48万
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环境致癌物诱导少数 MOMP 引发肺癌和间皮瘤的癌变,同时通过 Mcl-1 维持细胞凋亡抵抗
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  • 财政年份:
    2022
  • 资助金额:
    $ 31.48万
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对自凋亡外泌体的自然免疫在维持免疫稳态中的作用
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  • 资助金额:
    $ 31.48万
  • 项目类别:
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