Cardiac physiology at the cellular level: use of cultured HL-1 cardiomyocytes for studies of cardiac muscle cell structure and function

被引:344
作者
White, SM [1 ]
Constantin, PE [1 ]
Claycomb, WC [1 ]
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Dept Biochem & Mol Biol, New Orleans, LA 70112 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2004年 / 286卷 / 03期
关键词
heart muscle cell; cell culture; cell line;
D O I
10.1152/ajpheart.00986.2003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
HL-1 cells are currently the only cardiomyocyte cell line available that continuously divides and spontaneously contracts while maintaining a differentiated cardiac phenotype. Extensive characterization using microscopic, genetic, immunohistochemical, electrophysiological, and pharmacological techniques has demonstrated how similar HL-1 cells are to primary cardiomyocytes. In the few years that HL-1 cells have been available, they have been used in a variety of model systems designed to answer important questions regarding cardiac biology at the cellular and molecular levels. Whereas HL-1 cells have been used to study normal cardiomyocyte function with regard to signaling, electrical, metabolic, and transcriptional regulation, they have also been used to address pathological conditions such as hypoxia, hyperglycemia-hyperinsulinemia, apoptosis, and ischemia-reperfusion. The availability of an immortalized, contractile cardiac cell line has provided investigators with a tool for probing the intricacies of cardiomyocyte function. In this review, we describe the culture and characterization of HL-1 cardiomyocytes as well as various model systems that have been developed using these cells to gain a better understanding of cardiac biology at the cellular and molecular levels.
引用
收藏
页码:H823 / H829
页数:7
相关论文
共 62 条
[1]   Identification of a COOH-terminal segment involved in maturation and stability of human ether-a-go-go-related gene potassium channels [J].
Akhavan, A ;
Atanasiu, R ;
Shrier, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (41) :40105-40112
[2]   SAGE identification of differentiation responsive genes in P19 embryonic cells induced to form cardiomyocytes in vitro [J].
Anisimov, SV ;
Tarasov, KV ;
Riordan, D ;
Wobus, AM ;
Boheler, KR .
MECHANISMS OF DEVELOPMENT, 2002, 117 (1-2) :25-74
[3]  
ATLAS S A, 1985, Journal of Clinical Hypertension, V1, P187
[4]   Adrenomedullin is a regulated modulator of neonatal cardiomyocyte hypertrophy in vitro [J].
Autelitano, DJ ;
Ridings, R ;
Tang, F .
CARDIOVASCULAR RESEARCH, 2001, 51 (02) :255-264
[5]   Differentiation of pluripotent embryonic stem cells into cardiomyocytes [J].
Boheler, KR ;
Czyz, J ;
Tweedie, D ;
Yang, HT ;
Anisimov, SV ;
Wobus, AM .
CIRCULATION RESEARCH, 2002, 91 (03) :189-201
[6]   Burn plasma mediates cardiac myocyte apoptosis via endotoxin [J].
Carlson, DL ;
Lightfoot, E ;
Bryant, DD ;
Haudek, SB ;
Maass, D ;
Horton, J ;
Giroir, BP .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 282 (05) :H1907-H1914
[7]   The fission yeast Rad32 (Mre11)-Rad50-Nbs1 complex is required for the S-phase DNA damage checkpoint [J].
Chahwan, C ;
Nakamura, TM ;
Sivakumar, S ;
Russell, P ;
Rhind, N .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (18) :6564-6573
[8]   Transport characteristics of HL-1 cells: A new model for the study of adenosine physiology in cardiomyocytes [J].
Chaudary, N ;
Shuralyova, I ;
Liron, T ;
Sweeney, G ;
Coe, IR .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 2002, 80 (05) :655-665
[9]   Characterization of apoptosis signal transduction pathways in HL-5 cardiomyocytes exposed to ischemia/reperfusion oxidative stress model [J].
Cicconi, S ;
Ventura, N ;
Pastore, D ;
Bonini, P ;
Di Nardo, P ;
Lauro, R ;
Marlier, LNJL .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 195 (01) :27-37
[10]   HL-1 cells: A cardiac muscle cell line that contracts and retains phenotypic characteristics of the adult cardiomyocyte [J].
Claycomb, WC ;
Lanson, NA ;
Stallworth, BS ;
Egeland, DB ;
Delcarpio, JB ;
Bahinski, A ;
Izzo, NJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :2979-2984