MITOCHONDRIAL COMPLEX 1 ACTIVITY IN MYOCARDIAL-SPECIFIC CHF1 DEFICIENT MICE Jeffrey Gordon 11/23/2010.

Slides:



Advertisements
Similar presentations
- D A N I S H A G I N G R E S E A R C H C E N T E R - Why do we age so differently? Tinna Stevnsner for Christina Poulsen Hvitby (on maternity.
Advertisements

Citric Acid Cycle 1 C483 Spring The net effect of the eight steps of the citric acid cycle is to A) completely oxidize an acetyl group to carbon.
Molecule of the Week ATP Synthase. ...a nanoscale machine ● Two molecular motors / generators ● Enzyme ● Ion pump Function: Synthesize ATP / Create proton.
CELLULAR RESPIRATION STATIONS Markley. STATION 1: OVERVIEW.
Pulse Oximetry Dr.C.N.Chandra Sekhar M.D. Oxygenation Oxygen tension Oxygen content Oxygen saturation.
Bioenergetics Lecture 5 summary Last time –integrating catabolic metabolism, review catabolism This time –similarities and differences.
The rate of electron transport in mitochondria is frequently measured by the disappearance of oxygen in a solution. Justify why this is a good method.
Packet #28 Chapter #9. Summary Thus Far… At the end of the Krebs Cycle, and before the cell makes more ATP at the electron transport chain, produced so.
Energy Generation in Mitochondria and Chloroplasts
Why Lactate is a Friend to Exercise. 1 st : Lactate & H+ temporal relationship b/w  in force & H+ accumulation at same time, metabolic products  : ADP,
Involvement of the Mitochondrial Calcium Uniporter in Cardioprotection by Ischemic Preconditioning.
Effect of oxygen on the Escherichia coli ArcA and FNR regulation systems and metabolic responses Chao Wang Jan 23, 2006.
Chapter 13 &14 Energy Generation in Mitochondria.
Citric Acid Cycle & Oxidative Phosphorylation The citric acid cycle, formerly known as the Kreb cycle, begins in the mitochondria as the 2 molecules of.
Chapter 16.2: The Citric Acid Cycle CHEM 7784 Biochemistry Professor Bensley.
Lesson 7: Harvesting of Energy “Cellular Respiration”
Apoptosis, controlled cell death, is a natural process of development. Recently it has been found that mitochondria play an important role in apoptosis.
Part 2: Transition Reaction
Introduction Dry eye is a condition in which there are insufficient tears to lubricate and nourish the eye. An estimated 25 million Americans are affected.
How Cells Harvest Chemical Energy
Nitric Oxide Synthase in Mouse Brain Tissue that Exhibits Alzheimer’s Disease Patrick McCarthy
AEROBIC METABOLISM II: ELECTRON TRANSPORT CHAIN Khadijah Hanim Abdul Rahman School of Bioprocess Eng, UniMAP Week 15: 17/12/2012.
8.3 READ Qs 1-IDENTIFY In the Kreb’s cycle what is pyruvate converted to? 2- IDENTIFY: Complete the figure by writing the location of each stage of cell.
Intro to Cellular Respiration, Glycolysis & Krebs Cycle
CELLULAR RESPIRATION. Overall Process C 6 H 12 O 6 + 6O 2  6CO 2 + 6H 2 O + ENERGY Purpose: Organisms routinely break down complex molecules in controlled.
Cellular Respiration Ch. 8
The Role of Electron Transport in Metabolism
How Cells Harvest Energy Chapter 6
Electron Transport Occurs on the Cristae or intermembrane of Mitochondria.
Chapter 19 Oxidative Phosphorylation Electron transferring (flow ) through a chain of membrane bound carriers (coupled redox reactions), generation of.
Why Lactate is a Friend to Exercise. 1 st : Lactate & H+ temporal relationship b/w  in force & H+ accumulation at same time, metabolic products  : ADP,
Glucose metabolism Some ATP Big bonus: NADH, FADH2 → REDUCING POWER
Chapter 7: Cellular Pathways That Harvest Chemical Energy Cellular Pathways That Harvest Chemical Energy Obtaining Energy and Electrons from GlucoseObtaining.
Metabolic Reactions Enzymology Catabolism Litho/Phototrophy Anabolism Microbial Metabolism.
How We Obtain Sufficient Coenzyme Q Benjamin Dahl Beloit College, Beloit, Wisconsin Abstract Avoiding Coenzyme Q (CoQ) deficiency is important because.
Lecture 19: Cellular Respiration. By the end of this lecture you should be able to… Describe respiration as a redox reaction. Concepts and terms: reductant,
Binding ADP + P i Synthesizing ATP Releasing ATP The binding-change mechanism or rotational catalysis (Paul Boyer, 1980s)‏ Each  subunit will take.
Cell Respiration C 6 H 12 O O H 2 O  6 CO H 2 O + ATP.
Chapter 6 Acquiring Energy.
BRG-1 in Cancer BRG-1 is an ATPase subunit of the SWI/SNF class of chromatin remodeling complexes It has been found mutated in a number of cancer cell.
Chromatin remodelling ATPase Brg1 is an essential factor for the maintenance of the intestinal crypt stem cell and adenoma formation Aliaksei Holik.
Cellular Respiration Chapter 7. Cellular Respiration Glycolysis and Fermentation Aerobic Respiration.
Mitochondrial function is essential for life. Increasing attention is paid to mitochondrial dysfunction as this is coupled to many metabolic and age-related.
How Cells Harvest Chemical Energy
Mitochondria and Autism
Mitochondria nitric oxide synthase in inflammation and septic shock Tu jie.
Ch. 6 Cellular Respiration 6.6 – Redox reactions release energy when electrons fall from a hydrogen carrier to oxygen Where do all the electrons.
Citric acid cycle and respiratory chain Pavla Balínová.
Åsa Gustafsson Research Interests Cardiovascular Disease Pathways that regulate life and death of cardiac myocytes Regulation of mitochondrial dynamics.
Lab2 Lactate Dehydrogenase Quantitative determination of lactate dehydrogenase LDH Daheeya AlEnazi.
Chapter 6 Cellular Respiration. Outline Day 1 –Energy Flow and Carbon Cycling –Overview of Energy Metabolism –Redox Reactions –Electrons and Role of Oxygen.
GRK2 Inhibition Reduces Post-Myocardial Infarction Cardiac Fibroblast-Mediated Adverse Remodeling Jennifer L. Philip 1, Xianyao Xu 1,Mei Han 1, Jinju Li.
Chromatin remodelling ATPase Brg-1 is an essential factor for the maintenance of the intestinal crypt stem cell and adenoma formation Aliaksei Holik.
Abstract In response to numerous pathologic stimuli, the myocardium undergoes a hypertrophic response characterized by increased.
C 6 H 12 O O H 2 O  6 CO H 2 O + ATP.
AP Biology Cellular Respiration Overview Part 1. Process of Cellular Respiration.
Regional Citrate Anticoagulation Limits Sepsis-Associated Tissue Injury Through The Decreased Release Of Microvesicles From Activated Leukocytes And Platelets.
Cellular Respiration Cell Respiration Step 1 :Krebs Cycle
Anaerobic respiration
Normal And Abnormal Cardiac Muscle Metabolism
F. Electron Transport Chain [ETC]
Lab2 Lactate Dehydrogenase
Cellular Respiration Ch. 4.4 – 4.5.
Figure 2 The potential effects of nicotinamide adenine
Volume 143, Issue 3, Pages (September 2012)
Volume 23, Issue 6, Pages (June 2016)
Nat. Rev. Cardiol. doi: /nrcardio
Volume 14, Issue 1, Pages (July 2011)
Figure 2 Impaired mitochondrial capacity and function in heart failure
III. Enzymes.
Presentation transcript:

MITOCHONDRIAL COMPLEX 1 ACTIVITY IN MYOCARDIAL-SPECIFIC CHF1 DEFICIENT MICE Jeffrey Gordon 11/23/2010

CHF1 – A Brief Overview CHF1 is a basic-HLH transcription repressor which plays an important role in cardiovascular development CHF1 deficient mice are more susceptible to heart failure CHF1 myocardial transgenic mice are less susceptible to heart failure

My Project Hypothesis: differences of mitochondrial complex 1 activity may explain the phenotypic difference in susceptibility to heart failure in the myocardial specific CHF1 deficient mouse model Why investigate complex 1? Who cares / to what end?

 In heart failure, decreased mitochondrial content and overall mitochondrial dysfunction exist  There are increased RNA transcripts of complex 1 in CHF1 transgenic mice  Preliminary data suggests decreased mitochondrial respiration in CHF1 deficient mice  Complex I is a manageable target Why Test Complex 1 ?

Mitochondria  Mitochondria generate most of a cell’s ATP.  Mitochondria have a more broad function  Made of 4 complexes and ATP synthase

Complex I  Largest complex – 45 different polypeptides  Redox reaction – NADH + H(+) + ubiquinone (Q) NAD(+) + dihydroubiquinone (QH2)

Who Cares / to what end?  Further characterize the mechanism responsible for increased susceptibility to heart failure of CHF1 deficient mice  Further understand mitochondria, which may offer therapeutic targets in the future

Overview of My Project 1. Breed wild-type controls and myocardial-specific CHF1 deficient mice 2. Isolate left ventricular mitochondrial tissue 3. Measure complex 1 activity via spectrophotometry 4. Normalize this to total mitochondrial activity 5. Compare the two groups

Spectrophotometry for Complex 1  Beer - Lambert Law  Measure light absorbance of a material to calculate concentration.  For complex 1: NADH + H(+) + ubiquinone (Q) NAD(+) + dihydroubiquinone (QH2) ?exp_id=187&section_id=13&name_id=245&template=teaching

Results GenotypeC1 activityC1/CS F/F aMHC-Cre F/F aMHC-Cre F/F aMHC-Cre F/F aMHC-Cre F/F aMHC-Cre F/F F/F F/F F/F F/F F/F F/F F/F F/F C1 = complex 1. CS = citrate synthase. -C1 Activity measured in nm/ (min *mg)

Results CHF1 Deficient WT P Value:

Conclusions  Complex 1 activity is not significantly different between wild-type and myocardial specific CHF- 1 deficient mice  Thus, differences in complex 1 are unlikely to explain the increased susceptibility to heart failure between these groups

Future Avenues  CHF1 deficient mice have abnormal with calcium signaling and apoptosis. Further studies into mitochondrial dysfunction may lead to better understandings of these mechanisms.