Na/Ca exchanges are powerful Ca transporters which strongly influence cardiac contractile and electrical activity, as well as secretion and contraction in other tissues. Our goal is an improved understanding of cardiac (NXC1) Na/Ca exchange function and regulation. Coupled to this goal are two further goals which transcend the scope of the proposal: the development of improved methods to study ion transport, including electroneutral transporters; and an understanding of phosphatidylinositol signaling in the control of surface membrane ion transport. 1) Transport function. To allow structure-function studies by a chimeric approach, the altered transport and gating properties of NCX1 homologues from squid (NCX-SQ1), drosophila (Calx), and arabidopsis will be analyzed. To verify an alternating access model of ion transport, we will test whether individual residues, mutated to cysteine or histidine change their accessibility from inside to outside when ions are transported. 2) Exchanger regulation. The molecular basis of exchanger modulation by phosphatidylinositol-4'-5'-biphosphate (PIP2) will be analyzed, and exchanger regulatory mechanisms will be explored in light of preliminary data indicating potential regulation at the levels of (a) type 2 phosphatidylinositol-4'-kinase, (b) Gq-regulated phospholipase C, (c) lipid phosphatases, and (d) regulatory changes of PIP2 affinity. 3) Cellular function. The hypotheses will be tested that changes of cardiac frequency and stretch modulate Na/Ca exchange activity, and thereby contractility, via changes of PIP2. Our proposed studies has three significant methodological components: 1) Giant-patch and whole-cell methods for studies of Na/Ca exchange regulatory have been improved. 2) Fiber optic methods have been developed to monitor ion transport activity via concentration changes in an artificially restricted extracellular space. They will be validated by measurements of Na/H exchange activity, and they will be used to test for possible exchange stoichiometry changes and to verify different ion selectivities of the Arabidopsis exchanger. 3). A sensitive, non-radioactive method has been developed to quantify phospholipids, including phosphatidylinositides, on TLC plates. In total, therefore, our proposal is of broad physiological significance and is highly relevant to pathological roles of Ca in cardiac ischemia.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL051323-08
Application #
6343531
Study Section
Special Emphasis Panel (ZRG1-MDCN-4 (01))
Program Officer
Reinlib, Leslie
Project Start
1994-01-01
Project End
2003-12-31
Budget Start
2001-01-01
Budget End
2001-12-31
Support Year
8
Fiscal Year
2001
Total Cost
$292,084
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Physiology
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Fuster, Daniel; Moe, Orson W; Hilgemann, Donald W (2008) Steady-state function of the ubiquitous mammalian Na/H exchanger (NHE1) in relation to dimer coupling models with 2Na/2H stoichiometry. J Gen Physiol 132:465-80
Yaradanakul, Alp; Wang, Tzu-Ming; Lariccia, Vincenzo et al. (2008) Massive Ca-induced membrane fusion and phospholipid changes triggered by reverse Na/Ca exchange in BHK fibroblasts. J Gen Physiol 132:29-50
Wang, Tzu-Ming; Hilgemann, Donald W (2008) Ca-dependent nonsecretory vesicle fusion in a secretory cell. J Gen Physiol 132:51-65
Hilgemann, Donald W (2007) Local PIP(2) signals: when, where, and how? Pflugers Arch 455:55-67
Yaradanakul, Alp; Hilgemann, Donald W (2007) Unrestricted diffusion of exogenous and endogenous PIP(2 )in baby hamster kidney and Chinese hamster ovary cell plasmalemma. J Membr Biol 220:53-67
Yaradanakul, Alp; Feng, Siyi; Shen, Chengcheng et al. (2007) Dual control of cardiac Na+ Ca2+ exchange by PIP(2): electrophysiological analysis of direct and indirect mechanisms. J Physiol 582:991-1010
Shen, Chengcheng; Lin, Mei-Jung; Yaradanakul, Alp et al. (2007) Dual control of cardiac Na+ Ca2+ exchange by PIP(2): analysis of the surface membrane fraction by extracellular cysteine PEGylation. J Physiol 582:1011-26
Hilgemann, Donald W (2007) On the physiological roles of PIP(2) at cardiac Na+ Ca2+ exchangers and K(ATP) channels: a long journey from membrane biophysics into cell biology. J Physiol 582:903-9
Hilgemann, Donald W; Yaradanakul, Alp; Wang, Yong et al. (2006) Molecular control of cardiac sodium homeostasis in health and disease. J Cardiovasc Electrophysiol 17 Suppl 1:S47-S56
Fuster, Daniel; Moe, Orson W; Hilgemann, Donald W (2004) Lipid- and mechanosensitivities of sodium/hydrogen exchangers analyzed by electrical methods. Proc Natl Acad Sci U S A 101:10482-7

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