18 results on '"MacRae, Calum"'
Search Results
2. Arrhythmogenic right ventricular cardiomyopathy mutations alter shear response without changes in cell–cell adhesion.
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Hariharan, Venkatesh, Asimaki, Angeliki, Michaelson, Jarett E., Plovie, Eva, MacRae, Calum A., Saffitz, Jeffrey E., and Huang, Hayden
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ARRHYTHMIA diagnosis ,CARDIOMYOPATHIES ,HEART disease genetics ,CELL adhesion inhibition ,CELLULAR control mechanisms ,GENETICS - Abstract
Aims The majority of patients diagnosed with arrhythmogenic right ventricular cardiomyopathy (ARVC) have mutations in genes encoding desmosomal proteins, raising the possibility that abnormal intercellular adhesion plays an important role in disease pathogenesis. We characterize cell mechanical properties and molecular responses to oscillatory shear stress in cardiac myocytes expressing mutant forms of the desmosomal proteins, plakoglobin and plakophilin, which are linked to ARVC in patients. Methods and results Cells expressing mutant plakoglobin or plakophilin showed no differences in cell–cell adhesion relative to controls, while knocking down these proteins weakened cell–cell adhesion. However, cells expressing mutant plakoglobin failed to increase the amount of immunoreactive signal for plakoglobin or N-cadherin at cell–cell junctions in response to shear stress, as seen in control cells. Cells expressing mutant plakophilin exhibited a similar attenuation in the shear-induced increase in junctional plakoglobin immunoreactive signal in response to shear stress, suggesting that the phenotype is independent of the type of mutant protein being expressed. Cells expressing mutant plakoglobin also showed greater myocyte apoptosis compared with controls. Apoptosis rates increased greatly in response to shear stress in cells expressing mutant plakoglobin, but not in controls. Abnormal responses to shear stress in cells expressing either mutant plakoglobin or plakophilin could be reversed by SB216763, a GSK3β inhibitor. Conclusions Desmosomal mutations linked to ARVC do not significantly affect cell mechanical properties, but cause myocytes to respond abnormally to mechanical stress through a mechanism involving GSK3β. These results may help explain why patients with ARVC experience disease exacerbations following strenuous exercise. [ABSTRACT FROM AUTHOR]
- Published
- 2014
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3. The developmental basis of adult arrhythmia: atrial fibrillation as a paradigm.
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Kapur, Sunil and MacRae, Calum A.
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ARRHYTHMIA ,DEVELOPMENTAL biology ,ELECTROPHYSIOLOGY ,ATRIAL fibrillation ,GENETIC research - Abstract
Normal cardiac rhythm is one of the most fundamental physiologic phenomena, emerging early in the establishment of the vertebrate body plan. The developmental pathways underlying the patterning and maintenance of stable cardiac electrophysiology must be extremely robust, but are only now beginning to be unraveled. The step-wise emergence of automaticity, AV delay and sequential conduction are each tightly regulated and perturbations of these patterning events is now known to play an integral role in pediatric and adult cardiac arrhythmias. Electrophysiologic patterning within individual cardiac chambers is subject to exquisite control and is influenced by early physiology superimposed on the underlying gene networks that regulate cardiogenesis. As additional cell populations migrate to the developing heart these too bring further complexity to the organ, as it adapts to the dynamic requirements of a growing organism. A comprehensive understanding of the developmental basis of normal rhythm will inform not only the mechanisms of inherited arrhythmias, but also the differential regional propensities of the adult heart to acquired arrhythmias. In this review we use atrial fibrillation as a generalizable example where the various factors are perhaps best understood. [ABSTRACT FROM AUTHOR]
- Published
- 2013
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4. ACE I/D polymorphism associated with abnormal atrial and atrioventricular conduction in lone atrial fibrillation and structural heart disease: Implications for electrical remodeling.
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Watanabe, Hiroshi, Kaiser, Daniel W., Makino, Seiko, MacRae, Calum A., Ellinor, Patrick T., Wasserman, Brian S., Kannankeril, Prince J., Donahue, Brian S., Roden, Dan M., and Darbar, Dawood
- Abstract
Background: The angiotensin-converting enzyme (ACE) gene contains a common polymorphism based on the insertion (I) or deletion (D) of a 287-bp intronic DNA fragment. The D allele is associated with higher ACE activity and thus higher angiotensin II levels. Angiotensin II stimulates cardiac fibrosis and conduction heterogeneity. Objective: The purpose of this study was to determine whether the ACE I/D polymorphism modulates cardiac electrophysiology. Methods: Three different cohorts of patients were studied: 69 patients with paroxysmal lone atrial fibrillation (AF), 151 patients with structural heart disease and no history of AF, and 161 healthy subjects without cardiovascular disease or AF. Patients taking drugs that affect cardiac conduction were excluded from the study. ECG parameters during sinus rhythm were compared among the ACE I/D genotypes. Results: The ACE I/D polymorphism was associated with the PR interval and heart block in the lone AF cohort. In multivariable linear regression models, the D allele was associated with longer PR interval in the lone AF and heart disease cohorts (12.0-ms and 7.1-ms increase per D allele, respectively). P-wave duration showed a similar trend, with increase in PR interval across ACE I/D genotypes in the lone AF and heart disease cohorts. Conclusion: The ACE D allele is associated with electrical remodeling in patients with lone AF and in those with heart disease, but not in control subjects. ACE activity may play a role in cardiac remodeling after the development of AF and heart disease. [Copyright &y& Elsevier]
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- 2009
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5. Zebrafish genetic models for arrhythmia
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Milan, David J. and MacRae, Calum A.
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ZEBRA danio , *ARRHYTHMIA , *ELECTROPHYSIOLOGY , *MORPHOGENESIS - Abstract
Abstract: Over the last decade the zebrafish has emerged as a major genetic model organism. While stimulated originally by the utility of its transparent embryos for the study of vertebrate organogenesis, the success of the zebrafish was consolidated through multiple genetic screens, sequencing of the fish genome by the Sanger Center, and the advent of extensive genomic resources. In the last few years the potential of the zebrafish for in vivo cell biology, physiology, disease modeling and drug discovery has begun to be realized. This review will highlight work on cardiac electrophysiology, emphasizing the arenas in which the zebrafish complements other in vivo and in vitro models; developmental physiology, large-scale screens, high-throughput disease modeling and drug discovery. Much of this work is at an early stage, and so the focus will be on the general principles, the specific advantages of the zebrafish and on future potential. [Copyright &y& Elsevier]
- Published
- 2008
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6. Cardiac sodium channel mutation in atrial fibrillation.
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Ellinor, Patrick T., Nam, Edwin G., Shea, Marisa A., Milan, David J., Ruskin, Jeremy N., and MacRae, Calum A.
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Background: Mutations in the sodium channel SCN5A have been implicated in many cardiac disorders, including the long QT syndrome, Brugada syndrome, conduction system disease, and dilated cardiomyopathy with atrial arrhythmias. Objective: In view of the pleiotropic effects of SCN5A mutations, the purpose of this study was to examine a cohort of patients with familial atrial fibrillation (AF) for mutations in the SCN5A gene. Methods: Probands with AF were enrolled in the study between June 1, 2001 and February 10, 2004. Each patient underwent a standardized evaluation, which included an interview, physical examination, ECG, echocardiogram, and blood sample for genetic analysis. Direct sequencing of the coding region of SCN5A was used to screen for mutations in genomic DNA. Results: One hundred eighty-nine patients with AF were enrolled during the study period. From this cohort, a subset of 57 probands with a family history of AF in at least one first-degree relative was studied. Forty-seven subjects were men (82%); 45 had paroxysmal AF (79%). Echocardiography revealed ejection fraction 62% ± 6.4 % and left atrial dimension 40 ± 6.9 mm. A single mutation (N1986K) was observed in one family but was not present in more than 600 control chromosomes. Expression of the N1986K mutant in Xenopus oocytes revealed a hyperpolarizing shift in channel steady-state inactivation. Conclusion: In a cohort with familial AF, a single SCN5A mutation causing the arrhythmia in one kindred was identified. These data extend the range of phenotypes observed with SCN5A mutations and suggest that variation in the SCN5A gene is not a major cause of familial AF. [Copyright &y& Elsevier]
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- 2008
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7. Genetics of atrial fibrillation.
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Ellinor, Patrick T., Choudry, Subbarao, and MacRae, Calum A.
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ATRIAL fibrillation ,ATRIAL arrhythmias ,HEART diseases ,ARRHYTHMIA ,CLINICAL medicine ,ETIOLOGY of diseases ,GENETICS - Abstract
Atrial fibrillation (AF) is the most common arrhythmia encountered in clinical practice. Despite its prevalence, relatively little is known regarding the primary mechanisms of AF and, therefore, current treatment practices focus mainly on controlling the disorder and preventing its complications once it is already present. The study of the pathogenesis of AF is complicated by the varied clinical presentation of the arrhythmia and its coexistence with other cardiac pathologies. This article reviews current efforts to delineate the fundamental mechanisms of AF, with a focus on genetic studies. Identification of the underlying etiology may result in the development of more targeted and effective therapies for AF. [ABSTRACT FROM AUTHOR]
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- 2006
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8. Arrhythmogenic right ventricular cardiomyopathy: moving toward mechanism.
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MacRae, Calum A., Birchmeier, Walter, and Thierfelder, Ludwig
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CARDIOMYOPATHIES , *GENETIC mutation , *ARRHYTHMIA , *DYSPLASIA , *HEART cells , *PATHOLOGICAL physiology - Abstract
Mutations in genes encoding desmosomal proteins have been identified as the major cause of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC), in which the right ventricle is ‘replaced’ by fibrofatty tissue, resulting in lethal arrhythmias. In this issue of the JCI, Garcia-Gras et al. demonstrate that cardiac-specific loss of the desmosomal protein desmoplakin is sufficient to cause nuclear translocation of plakoglobin, upregulation of adipogenic genes in vitro, and a shift from a cardiomyocyte to an adipocyte cell fate in vivo (see the related article beginning on page 2012). This evidence for potential Wnt/β-catenin signaling defects sets the scene for a comprehensive exploration of the contributions of this pathway to the pathophysiology of ARVC, not only through perturbation of cardiac patterning and development, but also through effects on myocardial differentiation and physiology. [ABSTRACT FROM AUTHOR]
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- 2006
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9. In vivo recording of adult zebrafish electrocardiogram and assessment of drug-induced QT prolongation.
- Author
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Milan, David J., Jones, Ian L., Ellinor, Patrick T., and Macrae, Calum A.
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ZEBRA danio ,ELECTROCARDIOGRAPHY ,MORPHOGENESIS ,ELECTRODES ,PROPRANOLOL ,PERFORMANCE-enhancing drugs ,PHYSIOLOGY - Abstract
In the last decade the zebrafish has become a major model organism for the study of development and organogenesis. To maximize the experimental utility of this organism, it will be important to establish methods for adult phenotyping. We previously proposed that the embryonic zebrafish may be useful in high-throughput screening for drug-induced cardiotoxicity. We now describe a method for the reproducible recording of the adult zebrafish ECG and illustrate its application in the investigation of QT-prolonging drugs. Zebrafish ECGs were obtained by inserting two needle electrodes through the ventral epidermis. Fish were perfused orally, and motion artifacts were eliminated with a paralytic dose of μ-conotoxin GIIIB. Test compounds were delivered via the perfusion system. Without a means of hydration and oxygenation, the fish succumb rapidly. The use of a perfusion system allowed stable recording for >6 h. Baseline conduction intervals were as follows: PR, 66 ms (SD 14); QRS, 34 ms (SD11); QT, 242 ms (SD 54); and R-R, 398 ms (SD 77). The known QT-prolonging agents astemizole, haloperidol, pimozide, and terfenadine caused corrected QT increases of 18% (SD 9), 16% (SD 11), 17% (SD 9), and 11% (SO 6), respectively. The control drugs clonidine, penicillin and propranolol did not prolong the corrected QT interval. In conclusion, perfusion and muscular paralysis allows stable, low-noise recording of zebrafish ECGs. Agents known to cause QT prolongation in humans caused QT prolongation in fish in each case. The development of rigorous tools for the phenotyping of adult zebrafish will complement the high-throughput assays currently under development for embryonic and larval fish. [ABSTRACT FROM AUTHOR]
- Published
- 2006
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10. Reduced apelin levels in lone atrial fibrillation.
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Ellinor, Patrick T., Low, Adrian F., and MacRae, Calum A.
- Abstract
Aims Apelin is an endogenous peptide hormone that appears to have a physiological role in counter-regulation of the angiotensin and vasopressin systems. This peptide has been reported to be down-regulated in subjects with acute heart failure, but has not been studied in other cardiovascular conditions. We studied apelin levels in 73 subjects with lone atrial fibrillation (AF). [ABSTRACT FROM PUBLISHER]
- Published
- 2006
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11. Potassium channel gene mutations rarely cause atrial fibrillation.
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Ellinor, Patrick T, Petrov-Kondratov, Vadim I, Zakharova, Elena, Nam, Edwin G, and MacRae, Calum A
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ATRIAL fibrillation ,POTASSIUM channels ,ARRHYTHMIA ,HEART diseases ,GENETIC polymorphisms - Abstract
Background: Mutations in several potassium channel subunits have been associated with rare forms of atrial fibrillation. In order to explore the role of potassium channels in inherited typical forms of the arrhythmia, we have screened a cohort of patients from a referral clinic for mutations in the channel subunit genes implicated in the arrhythmia. We sought to determine if mutations in KCNJ2 and KCNE1-5 are a common cause of atrial fibrillation. Methods: Serial patients with lone atrial fibrillation or atrial fibrillation with hypertension were enrolled between June 1, 2001 and January 6, 2005. Each patient underwent a standardized interview and physical examination. An electrocardiogram, echocardiogram and blood sample for genetic analysis were also obtained. Patients with a family history of AF were screened for mutations in KCNJ2 and KCNE1-5 using automated sequencing. Results: 96 patients with familial atrial fibrillation were enrolled. Eighty-three patients had lone atrial fibrillation and 13 had atrial fibrillation and hypertension. Patients had a mean age of 56 years at enrollment and 46 years at onset of atrial fibrillation. Eighty-one percent of patients had paroxysmal atrial fibrillation at enrollment. Unlike patients with an activating mutation in KCNQ1, the patients had a normal QT
c interval with a mean of 412 ± 42 ms. Echocardiography revealed a normal mean ejection fraction of 62.0 ± 7.2 % and mean left atrial dimension of 39.9 ± 7.0 mm. A number of common polymorphisms in KCNJ2 and KCNE1-5 were identified, but no mutations were detected. Conclusion: Mutations in KCNJ2 and KCNE1-5 rarely cause typical atrial fibrillation in a referral clinic population. [ABSTRACT FROM AUTHOR]- Published
- 2006
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12. Animal models for arrhythmias
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Milan, David J. and MacRae, Calum A.
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ARRHYTHMIA , *HEART beat , *PALPITATION , *ETIOLOGY of diseases - Abstract
Abstract: The complex pathophysiology of human arrhythmias has proven difficult to model. Direct correlations between the traditional arrhythmia mechanisms, including abnormal excitability, conduction, or repolarization and underlying molecular or cellular biology are poorly defined, as the primary etiologies of many human arrhythmias remain unknown. Since the causes of several arrhythmic syndromes have been identified, genetic models reproducing the mechanisms of these arrhythmias have become feasible. Initial murine modeling has revealed that in many cases the pathophysiology of the respective human disease is more complex than had been suspected. Insights from human genetic studies and animal models strongly suggest that the primary molecular defects may contribute at many stages in the causal chain leading to arrhythmia. The comprehensive analysis of each arrhythmia will require knowledge not only of the membrane effects of the primary defects, but also downstream intracellular signals, the developmental results of these perturbations, and the integration of compensatory responses and environmental factors. Precise modeling will require not only the mutation of specific residues in known disease genes, but also the systematic study of each of the many steps in arrhythmogenesis. Ultimately, such models will enable unbiased screens for disease mechanisms and novel therapies. [Copyright &y& Elsevier]
- Published
- 2005
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13. Clinical Subtypes of Lone Atrial Fibrillation.
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PATTON, KRISTEN K., ZACKS, ERAN S., CHANG, JOSEPH Y., SHEA, MARISA A., RUSKIN, JEREMY N., MACRAE, CALUM A., and ELLINOR, PATRICK T.
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ATRIAL fibrillation ,ATRIAL arrhythmias ,GENETICS ,DISEASES ,ARRHYTHMIA - Abstract
PATTON, K.K., et al.: Clinical Subtypes of Lone Atrial Fibrillation . Aims: In the face of increasing evidence of underlying genetic heterogeneity for lone atrial fibrillation (LAF), we undertook a clinical analysis of subjects to identify the phenotypic subsets of this arrhythmia. Methods and Results: We evaluated serial patients who presented with LAF between July 5, 2001 and December 19, 2003. Subjects underwent a standardized interview to elicit a detailed medical history, prior therapies, and precipitants of atrial fibrillation. The results of a physical exam, electrocardiogram and echocardiogram were reviewed. One hundred and eighty subjects with a mean age of 45 years (15–67 years) at the time of diagnosis were enrolled. The majority of patients originally presented with paroxysmal fibrillation (94%), and 7.8% progressed to permanent AF. Reported triggers for AF included sleeping (44%), exercise (36%), alcohol use (36%), and eating (34%). Women with LAF had distinct symptoms, triggers for episodic AF, and over one-fourth had an underlying rheumatologic condition. Several subsets of AF including familial AF (39%), exercise-induced AF (32%), and conduction system disease requiring pacemaker implantation (7%), were identified. Conclusions: Family history, exercise as a trigger of AF, and a history of a pacemaker identified subtypes of LAF. (PACE 2005; 28:630–638) [ABSTRACT FROM AUTHOR]
- Published
- 2005
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14. Molecular mechanisms in atrial fibrillation.
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Ellinor, Patrick T. and MacRae, Calum A.
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ATRIAL fibrillation ,HEART beat ,ARRHYTHMIA ,ETIOLOGY of diseases - Abstract
Atrial fibrillation is the most common, significant clinical arrhythmia, yet relatively little is known about the primary etiology of this condition and it remains difficult to treat or prevent. Atrial fibrillation induces remodeling of atrial myocytes that in turn helps to sustain the arrhythmia and increases susceptibility to recurrence. Recent work suggests that atrial fibrillation is a heterogeneous syndrome but subsets with specific etiologies are beginning to be uncovered. Identification of the discrete causes of atrial fibrillation will enable the development of targeted strategies for the prevention and treatment of this morbid disorder. [Copyright &y& Elsevier]
- Published
- 2005
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15. Electrophysiologic Characteristics of Accessory Atrioventricular Connections in an Inherited Form of Wolff-Parkinson-White Syndrome.
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Mehdirad, Ali A., Fatkin, Diane, DiMarco, John P., MacRae, Calum A., Wase, Abdul, Seidman, J.G., Seidman, Christine E., and Benson, D. Woodrow
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ELECTROPHYSIOLOGY ,ATRIOVENTRICULAR node ,WOLFF-Parkinson-White syndrome ,ARRHYTHMIA ,CARDIOMYOPATHIES ,CHROMOSOMES - Abstract
Introduction: A familial form of Wolff-Parkinson- White syndrome (WPW) occurs in association with hypertrophic cardiomyopathy and intraventricular conduction abnormalities. This syndrome, demonstrating autosomal dominant inheritance and segregating with a high degree of penetrance but variable expressivity, has been genetically linked to chromosome 7q3. The purpose of this study is to detail the electrophysiologic characteristics of accessory atrioventricular connections (AC) in four members of a kindred with this syndrome. Methods and Results: We clinically evaluated 32 members of a single kindred and identified 20 individuals with ventricular preexcitation, abnormal intraventricular conduction including complete AV block and/or ventricular hypertrophy. Genetic linkage analysis mapped the disease gene in this kindred to the chromosome 7q3 locus (maximum logarithm of the odds score = 6.88, θ = 0); recoinbination events in affected individuals reduced the genetic interval from 7 centimorgans (cM) to S cM. Electruphysiologic study of four individuals with preexciatation identified seven AC (1 right sided, 3 septal, and 3 left sided). All four individuals had inducible orthodromic tachycardia; while three had multiple AC. Bidirectional conduction was demonstrated in 6 of 7 AC. Successful ablation was accomplished in 5 of 7 AC. Conclusion: The electrophysiologic characteristics and location of AC in family members having this complex cardiac phenotype are similar to those seen in individuals with isolated WPW. Identification of WPW in more than one family member should prompt clinical evaluation of relatives for additional findings of ventricular hypertrophy or conduction abnormalities. [ABSTRACT FROM AUTHOR]
- Published
- 1999
- Full Text
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16. Nr2f1a maintains atrial nkx2.5 expression to repress pacemaker identity within venous atrial cardiomyocytes of zebrafish.
- Author
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Martin, Kendall E., Ravisankar, Padmapriyadarshini, Beerens, Manu, MacRae, Calum A., and Waxman, Joshua S.
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GENE expression , *ARRHYTHMIA , *CONGENITAL heart disease , *BRACHYDANIO , *ATRIUMS (Architecture) , *REGULATOR genes , *ATRIAL arrhythmias - Abstract
Maintenance of cardiomyocyte identity is vital for normal heart development and function. However, our understanding of cardiomyocyte plasticity remains incomplete. Here, we show that sustained expression of the zebrafish transcription factor Nr2f1a prevents the progressive acquisition of ventricular cardiomyocyte (VC) and pacemaker cardiomyocyte (PC) identities within distinct regions of the atrium. Transcriptomic analysis of flow-sorted atrial cardiomyocytes (ACs) from nr2f1a mutant zebrafish embryos showed increased VC marker gene expression and altered expression of core PC regulatory genes, including decreased expression of nkx2.5, a critical repressor of PC differentiation. At the arterial (outflow) pole of the atrium in nr2f1a mutants, cardiomyocytes resolve to VC identity within the expanded atrioventricular canal. However, at the venous (inflow) pole of the atrium, there is a progressive wave of AC transdifferentiation into PCs across the atrium toward the arterial pole. Restoring Nkx2.5 is sufficient to repress PC marker identity in nr2f1a mutant atria and analysis of chromatin accessibility identified an Nr2f1a-dependent nkx2.5 enhancer expressed in the atrial myocardium directly adjacent to PCs. CRISPR/Cas9-mediated deletion of the putative nkx2.5 enhancer leads to a loss of Nkx2.5-expressing ACs and expansion of a PC reporter, supporting that Nr2f1a limits PC differentiation within venous ACs via maintaining nkx2.5 expression. The Nr2fdependent maintenance of AC identity within discrete atrial compartments may provide insights into the molecular etiology of concurrent structural congenital heart defects and associated arrhythmias. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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17. The zebrafish as a novel animal model to study the molecular mechanisms of mechano-electrical feedback in the heart
- Author
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Werdich, Andreas A., Brzezinski, Anna, Jeyaraj, Darwin, Khaled Sabeh, M., Ficker, Eckhard, Wan, Xiaoping, McDermott, Brian M., MacRae, Calum A., and Rosenbaum, David S.
- Subjects
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PHYSIOLOGICAL control systems , *HEART physiology , *LABORATORY zebrafish , *MOLECULAR biology , *ELECTROPHYSIOLOGY , *CARDIOVASCULAR diseases , *HYPERTROPHY , *ARRHYTHMIA - Abstract
Abstract: Altered mechanical loading of the heart leads to hypertrophy, decompensated heart failure and fatal arrhythmias. However, the molecular mechanisms that link mechanical and electrical dysfunction remain poorly understood. Growing evidence suggest that ventricular electrical remodeling (VER) is a process that can be induced by altered mechanical stress, creating persistent electrophysiological changes that predispose the heart to life-threatening arrhythmias. While VER is clearly a physiological property of the human heart, as evidenced by “T wave memory”, it is also thought to occur in a variety of pathological states associated with altered ventricular activation such as bundle branch block, myocardial infarction, and cardiac pacing. Animal models that are currently being used for investigating stretch-induced VER have significant limitations. The zebrafish has recently emerged as an attractive animal model for studying cardiovascular disease and could overcome some of these limitations. Owing to its extensively sequenced genome, high conservation of gene function, and the comprehensive genetic resources that are available in this model, the zebrafish may provide new insights into the molecular mechanisms that drive detrimental electrical remodeling in response to stretch. Here, we have established a zebrafish model to study mechano-electrical feedback in the heart, which combines efficient genetic manipulation with high-precision stretch and high-resolution electrophysiology. In this model, only 90 min of ventricular stretch caused VER and recapitulated key features of VER found previously in the mammalian heart. Our data suggest that the zebrafish model is a powerful platform for investigating the molecular mechanisms underlying mechano-electrical feedback and VER in the heart. [Copyright &y& Elsevier]
- Published
- 2012
- Full Text
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18. C-Reactive Protein in Lone Atrial Fibrillation
- Author
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Ellinor, Patrick T., Low, Adrian, Patton, Kristen K., Shea, Marisa A., and MacRae, Calum A.
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ATRIAL fibrillation , *C-reactive protein , *HYPERTENSION , *ARRHYTHMIA - Abstract
An inflammatory cause of atrial fibrillation (AF) has been proposed on the basis of the presence of lymphocytic infiltrates in the biopsy results of patients with lone AF, alterations of C-reactive protein (CRP) and interleukin-6 levels in subjects with AF, and the time course of postoperative AF. Many previous studies exploring inflammatory factors in AF have been confounded by concomitant medical illnesses. Subjects with lone AF provide a unique opportunity to eliminate the effects of associated conditions. We therefore sought to determine CRP levels in homogenous cohorts of patients with lone AF or AF and hypertension. One hundred twenty-one subjects with lone AF, 52 subjects with AF and hypertension, and 75 control subjects were enrolled and studied. Plasma CRP levels were determined using a commercially available immunoassay. There was no significant difference in CRP levels between subjects with lone AF and controls (1.34 vs 1.21 mg/L, p = 0.18). CRP levels in subjects with AF and hypertension were elevated compared with those of controls and those of subjects with lone AF, although this difference was attributable to increased body mass indexes. CRP levels were not elevated in subjects with lone AF compared with controls. In conclusion, these findings clarify previous observations of elevations in CRP levels in subjects with AF and suggest that this marker of systemic inflammation is associated not with the arrhythmia per se, but rather with underlying cardiovascular disease. [Copyright &y& Elsevier]
- Published
- 2006
- Full Text
- View/download PDF
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