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The cardiac Na/Ca exchanger (NCX) is the principal Ca efflux mechanism in cardiac myocytes and plays an essential role in regulating cardiac contractility. Characterizing the exchanger's regulatory properties is important for understanding both normal cardiac physiology and the perturbations that occur in pathogenic conditions. This project focuses on the allosteric regulation of NCX activity by cytosolic Ca and its modulation by the cytoskeleton. The hypothesis guiding these studies is that allosteric Ca activation displays hysteresis so that activity becomes Ca-independent following NCXactivation (persistent Ca activation). We propose that the hysteresis is due to (a) cytoskeletal interactions involving the "beta repeat regions" of the NCX protein that restrict access of Ca to the regulatory binding sites and (b) interaction of PIP2 with the so- called XIP region of the NCX protein. The project has 5 specific aims directed toward the following goals: (1) Elevations in cytosolic [Na] induce a Ca-independent mode of NCXactivity. We will measure the [Na] dependence of this response and investigate the role of cytoskeletal interactions, PIP2 and XIP mutations in the development of this activity. (2) We will determine whether stimulation of F-actin dynamics by protein kinase C, NO donors or activated Rac or Cdc42 enhances the development of Ca-independent activity and accelerates the rate of allosteric Ca activation. (3) We will determine how cytoskeletal interactions, cytosolic [Na] and PIP2 influence the development and relaxation of persistent Ca activation. (4) Mutations will be created in the beta repeat regions of the exchanger and their influence on cytoskeletal interactions, allosteric Ca activation and Ca-independent NCX activity will be assessed. (5) We will determine whether cytoskeletal interactions modulate NCX activity In rat neonatal and adult cardiac myocytes. Transfected CHO cells will be used in Aims 1-4. Digital imaging techniques using fluorescent Ca probes will be used to measureNCX transport activity.
期刊论文(28)
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Physiological and molecular characterization of the Na+/Ca2+ exchanger in human platelets.
人血小板中 Na /Ca2 交换器的生理和分子特征。
DOI: 10.1152/ajpheart.1999.277.3.h911
发表时间: 1999
期刊: The American journal of physiology
影响因子: --
作者: [Kimura,M, Jeanclos,EM, Donnelly,RJ, Lytton,J, Reeves,JP, Aviv,A]
通讯作者: Aviv,A
Regulation of the cardiac L-type calcium channel in L6 cells by arginine-vasopressin.
精氨酸加压素对 L6 细胞中心脏 L 型钙通道的调节。
DOI: 10.1042/bj20060742
发表时间: 2006
期刊: The Biochemical journal
影响因子: --
作者: [Hantash,BasilM, Thomas,AndrewP, Reeves,JohnP]
通讯作者: Reeves,JohnP
Acceleration of sodium-calcium exchange activity during ATP-induced calcium release in transfected Chinese hamster ovary cells.
转染的中国仓鼠卵巢细胞中 ATP 诱导的钙释放过程中钠钙交换活性的加速。
DOI: 10.1085/jgp.109.1.53
发表时间: 1997
期刊: The Journal of general physiology
影响因子: --
作者: [Vázquez,M, Fang,Y, Reeves,JP]
通讯作者: Reeves,JP
DOI: 10.1085/jgp.200308915
发表时间: 2003-11
期刊: The Journal of general physiology
影响因子: --
作者: [Reeves JP, Condrescu M]
通讯作者: Condrescu M
12
    REGULATION OF THE CARDIAC NA+/CA++ EXCHANGER
    REGULATION OF THE CARDIAC NA+/CA++ EXCHANGER
    REGULATION OF THE CARDIAC NA+/CA+2 EXCHANGER
    REGULATION OF THE CARDIAC NA+/CA+2 EXCHANGER
    海外基金