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![Page 1: Oxidative Inhibition of Erythrocyte Na + -K + Pump: A Functionally Relevant Circulating Marker of Oxidative Stress Dr. Chia-chi Liu Molecular Cardiac Research.](https://reader030.fdocuments.us/reader030/viewer/2022032607/56649ec55503460f94bcfa32/html5/thumbnails/1.jpg)
Oxidative Inhibition of Erythrocyte Na+-K+ Pump: A Functionally Relevant Circulating Marker of
Oxidative Stress
Dr. Chia-chi LiuMolecular Cardiac Research Unit
Sydney Medical School University of Sydney Australia
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Outline
• Cardiovascular disease (CVD) • CVD and Na pump• Background of Na pump• Oxidative regulation of the pump• Measurement of oxidative damage of Na
pump- a potential biomarker
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• the number 1 cause of death globally• accounting for 17.3 million deaths per year• a number that is expected to grow to >23.6 million by 2030
Cardiovascular disease (CVD)
http://www.who.int/cardiovascular_diseases/en/
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Overview
• Reactive oxygen species: key feature of cardiovascular disease
• Antioxidants fail to prevent cardiovascular morbidity and mortality
• Complexity of ROS signalling
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60
80
100
120
140
160
5 7 9 11 13 15 17 19
[Na]i
Con
trac
tilit
y (%
con
trol
)
Non-failing FailingFailingFailing
DM Bers. Cardiac E-C Coupling. 2001
Raised levels of cardiac myocyte Na+
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• Plasma membrane ion transporter
• Transports 3Na+ out- and 2K+ into cells
• Uses ~20% of all energy (ATP) in body
• Crucial for normal function and survival of all cells, especially for cardiac myocytes
The Na+-K+ pump
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3D structure of the Na+-K+ pump
Nature 459:446-50, 2009
a
bFXYD
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• Kinases mediate Na+-K+ pump regulation - however, kinases have poor access to
phosphorylation sites on the pump molecule
• Chemical oxidants decrease Na+-K+ pump activity
Na+-K+ pump Regulation
-Bibert S & Geering K. J Biol Chem 2008-Sweadner & Feschenko. Am J Physiol Cell Physiol 2001-Cornelius, et al. J Bioenerg Biomembr 2001
-Ellis DZ, Rabe J, Sweadner KJ. J Neurosci 2003-White CN et al. Am J Physiol Cell Physiol 2008
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Trends in Cardiovascular Medicine. 20(3):85-90, 2010
Oxidative protein modifications
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Protein Glutathionylation
• Protein glutathionylation -
– adduct with –ve charge– is stable but reversible
Liu, C.C. Circ Res 105, 693-700; 2009
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Glutathionylation of Na+-K+ pump
Total Cell Protein GSS- Protein -ve control
Biotin-GSH/streptavidin technique
Baseline
Protein Biotin-GSS
StreptavidinStreptavidin
0.0
0.5
1.0
1.5
2.0
2.5
3.0
3.5
Control ONOO-
*
GS
S-
1(f
old
)
Protein Biotin-GSS
StreptavidinStreptavidin
GS
S-
1(f
old
)
0.0
1.0
2.0
3.0
4.0
5.0
Control 0.2 mM ONOO-
0.5 mM ONOO-
*
*
IP: 1
IB: 1
IB: GSH
Protein GSSAntibodyAntibody
Liu, C.C. Circ Res 105, 693-700; 2009
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ControlONOO-
WT
Overexpression ofXenopus a1/b1 by cRNA
injection in oocytes
Liu, C.C. Circ Res 105, 693-700; 2009
Mutation of Cys45 in b1 subunit
Two–electrodevoltage-clamp
for measurementof pump current
vs.
Cys→Trp mutation eliminates ONOO--induced pump inhibition
Cys45→Trpmutation
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Only Cys 45 in b1 subunit
C45
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Would knowing the degree of oxidative inhibition of the Na+-K+ pump in erythrocytes help to monitor
the heart disease progress?
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IB: b1
TL IP: b1 + DTT IP: b1 IP: IgG
IB: GSH ~55 kDa
~55 kDa
Protein GSSAntibodyAntibody
b1 subunit is detectable in erythrocytes, and is glutathionylated
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Natasha Fry PhD in progress; Unpublished, 2014
Sham HFSham HF
Protein GSSAntibodyAntibody
Sham HF
Total Lysate IP: b1 IP: IgG
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Enzyme Linked Immunosorbent Assay - to quantify eb1-GSS
-GSH
RBC membrane proteins
b1 subunit-
B. Plate assayPatient A Patient B
A. Method
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eb1-GSS in HF vs sham rabbits
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Liu, Unpublished, 2014
Correlation of eb1-GSS with b1 subunit glutathionylation in cardiac myocytes
r=0.851; p<0.001
How does eb1-GSS relate to what’s happening in the heart?
3 Na+
2 K+
[Na+][K+]
[Cl-]
[Na+][K+]
[Cl-]
[Na+][K+]
[Cl-]
[Na+][K+]
[Cl-]
V
A
V
A
DRUG
DRUG
Vm = ECl = -14 mV
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How does eb1-GSS relate to what’s happening in the heart?
B-type Natriuretic Peptide (BNP)
LV systolic function
Natasha Fry PhD in progress; Unpublished, 2014
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Protein GSSAntibodyAntibody
Detection of eb1-GSS in humans
What about in humans?
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eb1-GSS HF patients vs. control
3167 ± 164 U vs 1018 ± 20 U; n=16; p<0.001Independent of age, gender, bmi.
What about in humans?......eb1-GSS
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Na-K ATPase activity in erythrocytes from HF patients vs. control
What about in humans?......Na+-K+-ATPase activity
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What about in humans? BNP
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Diabetes and eb1-GSS in animal models
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Diabetes and animal models
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Diabetes and eb1-GSS in humans
IB: b1
TL IP: b1 + DTT IP: b1 IP: IgG
IB: GSH
S-glutathionylation of erythrocyte β1 subunits detected in human.
S-glutathionylation of erythrocyte β1 subunits detected by ELISA. S-glutathionylation of
erythrocytes was significantly increased in DM patients compared to Normal .)
N DM0
50
100
150
200
eb1_
GSS
(%)
Human Model:
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Summary: eb1-GSS
• occurs and is detectable! • ELISA assay is rapid and quantitative• parallels oxidative inhibition of cardiac Na+-K+ pump• increases in patients with HF and reflects severity• increases in diabetics
Liu, Unpublished, 2014
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Potential prognostic value of eb1-GSS?
• For HF: important if being used as diagnostic tool, but less so if combined with clinical and laboratory biomarkers for prognostic purposes
• Ongoing work: – Prognostic significance of eb1-GSS over conventional biomarkers and
risk factors: • in hospitalized HF/DM• in community subjects at high risk of HF (SCREEN-HF ~ 4000
subjects)
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Special Thanks
International - Prof Kaethi Geering (Switzerland)- Dr Stephanie Bibert (Switzerland)- A/Prof Francesca Marassi USA)- A/Prof Kathy Sweadner (USA)- A/Prof Flemming Cornelius (Demark)-Dr Henning Bundgaard (Denmark) -Astellas Pharma company (Japan)
North Shore Heart Research Group- Prof Helge Rasmussen - Prof Gemma Figtree - Dr Elisha Hamilton Molecular Cardiac Research Unit-Miss Chris Mozar
PHD students-Miss. Natasha Fry-Dr. Keyvan Karimi Galougahi-Mr. Alvaro Garcia
Honours student-Mr. William Hannam
Australia - Prof Robert Baxter - A/Prof Jan Gebicki - A/Prof Ronald J. Clarke- A/Prof Richard Payne
Funded by :National Heart Foundation Australia Heart Research Australia