Isolation of a spontaneously fusing BC3H1 muscle cell line: fusion alters the response to serum stimulation

被引:0
作者
Thomas Steenstrup
Kevin Hannon
机构
[1] Purdue University,Department of Basic Medical Sciences, School of Veterinary Medicine
关键词
BC3H1 cells; muscle differentiation; myoblast fusion; growth factor; MyoD;
D O I
10.1290/1071-2690(2000)036<0241:IOASFB>2.0.CO;2
中图分类号
学科分类号
摘要
Differentiation of skeletal muscle cells involves two distinct events: exit from the cell cycle and expression of musclespecific contractile genes and formation of multinucleated myocytes. Although many studies have shown that growth factors regulate the initial step of differentiation, little is known about regulation of fusion. BC3H1 cells are a skeletal muscle cell line characterized by a nonfusing phenotype and an ability to dedifferentiate. When subjected to serum or growth factors, differentiated BC3H1 cells lose muscle-specific gene expression and re-enter the cell cycle. In this study, we describe a spontaneously fusing clone of BC3H1 cells. We demonstrate that this fusion capability is not due to altered muscle regulatory factor or adhesion molecule expression. Furthermore, we show that fusion inhibits dedifferentiation. Multinucleated BC3H1 cells do not lose myosin expression, nor do they re-enter the cell cycle. Fused BC3H1 cells react to serum stimulation with a hypertrophic response. Our results suggest that the state of differentiation, mono- or multinucleated, is essential to how myocytes react to growth stimulation and may provide a mechanism for how differentiation, fusion, and hypertrophy are regulated in vivo.
引用
收藏
页码:241 / 248
页数:7
相关论文
共 90 条
[1]  
Bader D.(1982)Immunochemical analysis of myosin heavy chain during avian myogenesis in vivo and in vitro J. Cell Biol. 95 763-770
[2]  
Masaki T.(1992)Expression of MRF4, a myogenic helix-loop-helix protein, produces multiple changes in the myogenic program of BC3H-1 cells Mol. Cell. Biol. 12 2482-2492
[3]  
Fischman D. A.(1990)Aberrant regulation of MyoD1 contributes to the partially defective myogenic phenotype of BC3H1 cells J. Cell Biol. 110 929-937
[4]  
Block N. E.(1995)Early stages of chick somite development Anat. Embryol. (Berl) 191 381-396
[5]  
Miller J. B.(1990)Enhanced myogenesis in NCAM-transfected mouse myoblasts Nature 344 348-351
[6]  
Brennan T. J.(1991)Expression of M-cadherin, a member of the cadherin multigene family, correlates with differentiation of skeletal muscle cells Proc. Natl. Acad. Sci. USA 88 8024-8028
[7]  
Edmondson D. G.(1989)A gene with homology to the myc similarity region of MyoD1 is expressed during myogenesis and is sufficient to activate the muscle differentiation program Genes Dev. 3 628-640
[8]  
Olson E. N.(1990)Expression of beta amyloid protein precursor mRNAs: recognition of a novel alternatively spliced form and quantitation in Alzheimer's disease using PCR Neuron 4 253-267
[9]  
Christ B.(1992)Temporal and quantitative analysis of myogenic regulatory and growth factor gene expression in the developing mouse embryo Dev. Biol. 151 137-144
[10]  
Ordahl C. P.(1988)The onset of myotome formation in the chick Anat. Embryol. 177 191-201