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Mechanisms of Receptor Regulated Na+-H+ Exchange

受体调节 Na -H 交换的机制

基本信息

批准号：
8667456
负责人：
DIANE L BARBER
金额：
$ 33.7万
依托单位：
UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
依托单位国家：
美国
项目类别：
财政年份：
1993
资助国家：
美国
起止时间：
1993-01-01 至 2015-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8667456
关键词：
1-Phosphatidylinositol 3-Kinase 6-Phosphofructokinase Acidosis Address Affect Affinity Animal Model Apoptosis Architecture Attenuated Binding Biochemical C-terminal Carcinoma Cardiac Cell Cycle Progression Cell Proliferation Cell membrane Cell physiology Cells Cerebral Ischemia Computer Simulation Cytoplasmic Tail Data Dependence Diabetes Mellitus Disseminated Malignant Neoplasm Drosophila eye Drosophila genus Enzymes Funding G2/M Transition Genetic Genetic Transcription Glycolysis Goals Grant Growth Factor Hematologic Neoplasms In Situ In Vitro Learning Malignant Neoplasms Mediating Mediator of activation protein Metabolic Metabolism Mitosis Mitotic Modeling Molecular NHE1 Necrosis Neoplasm Metastasis Normal Cell Normal Range Oncogene Activation Oncogenes Pathway interactions Phenotype Phosphatidylinositols Phosphorylation Phosphotransferases Physiological Play Protein Biochemistry Protein Dephosphorylation Proteins Regulation Retinal Role S Phase Signal Transduction Solid Neoplasm Structure Testing Therapeutic Time Tissues Tumor Suppressor Proteins base cancer cell cdc25 Phosphatase cell motility cell transformation cyclin B1 design driving force innovation macromolecular assembly migration mutant overexpression prevent protein structure receptor scaffold sensor tumor progression tumorigenesis

项目摘要

DESCRIPTION (provided by applicant): Dynamic changes in intracellular pH (pHi) regulate a range of normal and pathological cell processes. Increased pHi promotes cell proliferation, differentiation, and migration, and decreased pHi induces apoptosis. Dysregulated pHi is thought to contribute to cancer progression, diabetes, and tissue damage after cardiac and cerebral ischemia. The long-term goals of this grant are to determine the regulation and function of pHi dynamics. The past four funding cycles focused on how H+ fluxes by the plasma membrane Na-H exchanger NHE1 are regulated and drive pHi dynamics. We also showed the functional significance of NHE1-dependent increases in pHi for cell proliferation, cell cycle progression, and cell migration. Despite the broad significance of pHi-dependent cell functions, we have limited understanding of how changes in pHi affect proteins and macromolecular assemblies. To address this limitation we recently began studying the structure and function of pH sensors, or proteins with activities or binding affinities that are sensitive to small physiological changes in pH. The current application applies what we collectively learned in the previous four funding cycles to determine the design principles and function of pH sensors regulating basic cell processes that are aberrant in cancer cells. Increased pHi is a hallmark of most cancers, regardless of the tissue origin or genetic background. This likely reflects a dependence on higher pHi for metabolic adaptation, increased proliferation, and metastasis. We will test the hypothesis that pH sensors controlling metabolism and cell cycle progression play critical roles in how NHE1 and pHi direct cell functions that are dysregulated in cancer. Our studies use an innovative comprehensive approach that bridges protein structure, protein biochemistry, and cell physiology. In Aim 1 we will determine how kinases controlling metabolism are regulated by NHE1. We will test predictions on how phosphoinositide 3-kinase is pH sensitive, based on our recent structural and biochemical findings that its p85 regulatory subunit is a pH sensor. We also will determine NHE1 regulation of phosphofructokinase 1 (PFK1), the first rate-limiting enzyme in glycolysis, which directly binds the C-terminal cytoplasmic domain of NHE1 and has extremely pH-sensitive activity. In Aim 2 we will determine how NHE1 promotes cell proliferation by focusing on our previous findings that H+ efflux by NHE1 times G2/M. We will test predictions on Wee1 as a putative pH sensor based on our new computational and biochemical data and on how cyclin B1 expression is attenuated in cells lacking NHE1 activity. In Aim 3 we will determine the role of NHE activity and dysregulated pHi in tumorigenesis using Drosophila models we generated. We will test predictions on how loss of Dnhe2 may be a synthetic lethal for transformed but not normal cells, and test rescue of phenotypes with mutant pH sensors generated in Aim 1 and 2. We also will ask whether over expression of Dnhe2 cooperates with oncogene activation or tumor suppressor deletion to induce metastatic cancer, and will use modifier screens to identify mediators of the Dnhe2 over expression phenotype.

描述（由申请人提供）：细胞内pH（pHi）的动态变化调节一系列正常和病理细胞过程。pHi升高促进细胞增殖、分化和迁移，pHi降低诱导细胞凋亡。失调的pHi被认为有助于癌症进展、糖尿病和心脏和脑缺血后的组织损伤。该补助金的长期目标是确定pHi动态的调节和功能。过去的四个资助周期集中在质膜Na-H交换器NHE 1的H+通量如何调节和驱动pHi动态。我们还显示了NHE 1依赖性pHi增加对细胞增殖、细胞周期进展和细胞迁移的功能意义。尽管pH依赖性细胞功能具有广泛的意义，但我们对pH变化如何影响蛋白质和大分子组装的理解有限。为了解决这一限制，我们最近开始研究pH传感器的结构和功能，或具有对pH的微小生理变化敏感的活性或结合亲和力的蛋白质。当前的应用程序应用了我们在前四个资助周期中共同学到的知识，以确定pH传感器的设计原理和功能，调节癌细胞中异常的基本细胞过程。pHi升高是大多数癌症的标志，无论组织来源或遗传背景如何。这可能反映了代谢适应、增殖增加和转移对较高pHi的依赖性。我们将测试这一假设，即控制代谢和细胞周期进程的pH传感器在NHE 1和pHi如何指导癌症中失调的细胞功能中发挥关键作用。我们的研究采用创新的综合方法，将蛋白质结构，蛋白质生物化学和细胞生理学联系起来。在目标1中，我们将确定NHE 1如何调节控制代谢的激酶。我们将测试预测磷酸肌醇3-激酶是如何pH敏感，根据我们最近的结构和生化研究结果，其p85调节亚基是一个pH传感器。我们还将确定NHE 1对磷酸果糖激酶1（PFK 1）的调节，PFK 1是糖酵解中的第一个限速酶，它直接结合NHE 1的C-末端胞质结构域，具有极强的pH敏感性活性。在目标2中，我们将确定NHE 1如何促进细胞增殖，重点是我们以前的发现，即H+流出NHE 1倍G2/M。我们将测试预测Wee 1作为一个假定的pH传感器基于我们的新的计算和生化数据，以及细胞周期蛋白B1的表达是如何在缺乏NHE 1活性的细胞衰减。在目标3中，我们将使用我们生成的果蝇模型确定NHE活性和失调的pHi在肿瘤发生中的作用。我们将测试关于Dnhe 2的丢失如何可能是转化但不是正常细胞的合成致死的预测，并测试Aim 1和2中产生的突变pH传感器对表型的拯救。我们还将询问是否Dnhe 2的过表达与癌基因激活或肿瘤抑制基因缺失合作，以诱导转移性癌症，并将使用修饰筛选来鉴定Dnhe 2过表达表型的介体。

项目成果

期刊论文数量（24）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

pH sensing by FAK-His58 regulates focal adhesion remodeling.

DOI：
10.1083/jcb.201302131
发表时间：
2013-09-16
期刊：
The Journal of cell biology
影响因子：
0
作者：
Choi CH;Webb BA;Chimenti MS;Jacobson MP;Barber DL
通讯作者：
Barber DL

Galpha12 differentially regulates Na+-H+ exchanger isoforms.

Galpha12 差异性调节 Na -H 交换异构体。

DOI：
10.1074/jbc.271.37.22604
发表时间：
1996
期刊：
The Journal of biological chemistry
影响因子：
0
作者：
Lin,X;Voyno-Yasenetskaya,TA;Hooley,R;Lin,CY;Orlowski,J;Barber,DL
通讯作者：
Barber,DL

Increased intracellular pH is necessary for adult epithelial and embryonic stem cell differentiation.

DOI：
10.1083/jcb.201606042
发表时间：
2016-11-07
期刊：
The Journal of cell biology
影响因子：
0
作者：
Ulmschneider B;Grillo-Hill BK;Benitez M;Azimova DR;Barber DL;Nystul TG
通讯作者：
Nystul TG

A human MAP kinase interactome.

DOI：
10.1038/nmeth.1506
发表时间：
2010-10
期刊：
NATURE METHODS
影响因子：
48
作者：
Bandyopadhyay, Sourav;Chiang, Chih-yuan;Srivastava, Jyoti;Gersten, Merril;White, Suhaila;Bell, Russell;Kurschner, Cornelia;Martin, Christopher H.;Smoot, Mike;Sahasrabudhe, Sudhir;Barber, Diane L.;Chanda, Sumit K.;Ideker, Trey
通讯作者：
Ideker, Trey

The Nck-interacting kinase NIK increases Arp2/3 complex activity by phosphorylating the Arp2 subunit.