Myocardial Notch Signaling Reprograms Cardiomyocytes to a Conduction-Like Phenotype

被引:73
作者
Rentschler, Stacey [1 ,2 ]
Yen, Alberta H. [1 ,2 ]
Lu, Jia [3 ]
Petrenko, Nataliya B. [1 ]
Lu, Min Min [1 ]
Manderfield, Lauren J. [2 ]
Patel, Vickas V. [1 ]
Fishman, Glenn I. [3 ]
Epstein, Jonathan A. [1 ,2 ]
机构
[1] Univ Penn, Cardiovasc Inst, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
[3] NYU, Sch Med, Leon H Charney Div Cardiol, New York, NY USA
关键词
action potentials; conduction; pacemakers; Purkinje; reprogramming; BIOLOGICAL PACEMAKER; PURKINJE-FIBERS; HCN CHANNELS; SYSTEM; HEART; CELLS; SPECIFICATION; EXPRESSION; LINEAGE; PROTEIN;
D O I
10.1161/CIRCULATIONAHA.112.103390
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Notch signaling has previously been shown to play an essential role in regulating cell fate decisions and differentiation during cardiogenesis in many systems including Drosophila, Xenopus, and mammals. We hypothesized that Notch may also be involved in directing the progressive lineage restriction of cardiomyocytes into specialized conduction cells. Methods and Results-In hearts where Notch signaling is activated within the myocardium from early development onward, Notch promotes a conduction-like phenotype based on ectopic expression of conduction system-specific genes and cell autonomous changes in electrophysiology. With the use of an in vitro assay to activate Notch in newborn cardiomyocytes, we observed global changes in the transcriptome, and in action potential characteristics, consistent with reprogramming to a conduction-like phenotype. Conclusions-Notch can instruct the differentiation of chamber cardiac progenitors into specialized conduction-like cells. Plasticity remains in late-stage cardiomyocytes, which has potential implications for engineering of specialized cardiovascular tissues. (Circulation. 2012; 126: 1058-1066.)
引用
收藏
页码:1058 / U140
页数:27
相关论文
共 36 条
[21]   Biphasic Development of the Mammalian Ventricular Conduction System [J].
Miquerol, Lucile ;
Moreno-Rascon, Natividad ;
Beyer, Sabrina ;
Dupays, Laurent ;
Meilhac, Sigolene M. ;
Buckingham, Margaret E. ;
Franco, Diego ;
Kelly, Robert G. .
CIRCULATION RESEARCH, 2010, 107 (01) :153-U344
[22]   A UNIFORM ENZYMATIC METHOD FOR DISSOCIATION OF MYOCYTES FROM HEARTS AND STOMACHS OF VERTEBRATES [J].
MITRA, R ;
MORAD, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 249 (05) :1056-1060
[23]   A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development [J].
Moskowitz, Ivan P. G. ;
Kim, Jae B. ;
Moore, Meredith L. ;
Wolf, Cordula M. ;
Peterson, Michael A. ;
Shendure, Jay ;
Nobrega, Marcelo A. ;
Yokota, Yoshifumi ;
Berul, Charles ;
Izumo, Seigo ;
Seidman, J. G. ;
Seidman, Christine E. .
CELL, 2007, 129 (07) :1365-1376
[24]   Cx30.2 enhancer analysis identifies Gata4 as a novel regulator of atrioventricular delay [J].
Munshi, Nikhil V. ;
McAnally, John ;
Bezprozvannaya, Svetlana ;
Berry, Jeff M. ;
Richardson, James A. ;
Hill, Joseph A. ;
Olson, Eric N. .
DEVELOPMENT, 2009, 136 (15) :2665-2674
[25]   ZO-1 determines adherens and gap junction localization at intercalated disks [J].
Palatinus, Joseph A. ;
O'Quinn, Michael P. ;
Barker, Ralph J. ;
Harris, Brett S. ;
Jourdan, Jane ;
Gourdie, Robert G. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2011, 300 (02) :H583-H594
[26]   Contactin-2 Expression in the Cardiac Purkinje Fiber Network [J].
Pallante, Benedetta A. ;
Giovannone, Steven ;
Fang-Yu, Liu ;
Zhang, Jie ;
Liu, Nian ;
Kang, Guoxin ;
Dun, Wen ;
Boyden, Penelope A. ;
Fishman, Glenn I. .
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY, 2010, 3 (02) :186-U107
[27]   Nkx2-5 pathways and congenital heart disease: Loss of ventricular myocyte lineage progressive cardiomyopathy and complete heart block [J].
Pashmforoush, M ;
Lu, JT ;
Chen, HY ;
St Amand, T ;
Kondo, R ;
Pradervand, S ;
Evans, SM ;
Clark, B ;
Feramisco, JR ;
Giles, W ;
Ho, SY ;
Benson, DW ;
Silberbach, M ;
Shou, WN ;
Chien, KR .
CELL, 2004, 117 (03) :373-386
[28]   Biological pacemaker implanted in canine left bundle branch provides ventricular escape rhythms that have physiologically acceptable rates [J].
Plotnikov, AN ;
Sosunov, EA ;
Qu, JH ;
Shlapakova, IN ;
Anyukhovsky, EP ;
Liu, LL ;
Janse, MJ ;
Brink, PR ;
Cohen, IS ;
Robinson, RB ;
Danilo, P ;
Rosen, MR .
CIRCULATION, 2004, 109 (04) :506-512
[29]   Expression and function of a biological pacemaker in canine heart [J].
Qu, JH ;
Plotnikov, AN ;
Danilo, P ;
Shlapakova, I ;
Cohen, IS ;
Robinson, RB ;
Rosen, MR .
CIRCULATION, 2003, 107 (08) :1106-1109
[30]   Neuregulin-1 promotes formation of the murine cardiac conduction system [J].
Rentschler, S ;
Zander, J ;
Meyers, K ;
France, D ;
Levine, R ;
Porter, G ;
Rivkees, SA ;
Morley, GE ;
Fishman, GI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10464-10469