Establishment of the mesodermal cell line QCE-6 - A model system for cardiac cell differentiation

被引:23
作者
Eisenberg, CA [1 ]
Bader, DM [1 ]
机构
[1] CORNELL UNIV, COLL MED, DEPT ANAT & CELL BIOL, NEW YORK, NY USA
关键词
cardiac development; mesoderm; cell line; growth factors;
D O I
10.1161/01.RES.78.2.205
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The QCE-6 cell line was derived from precardiac mesoderm of the Japanese quail. As previously reported, these cells are able to differentiate into two distinct cardiac cell types with myocardial or endocardial endothelial cell properties. This present communication describes in detail the derivation of this cell line and further characterizes the nontreated and induced myocardial and endothelial phenotypes of these cells. The QCE-6 cells exhibit an epithelial morphology, as well as the pattern of protein expression, that is characteristic of precardiac mesoderm. Treatment with retinoic acid, basic fibroblast growth factor (bFGF), transforming growth factor (TGF)-beta 2, and TGF-beta 3 induces these cells to differentiate and produce mixed cultures of epithelial and mesenchymal cells. The epithelial cells express myosin, desmin, and cardiac troponin I in a punctate pattern throughout the cytoplasm. These sarcomeric proteins become organized in a premyofibrillar pattern when TGF-beta 1, platelet-derived growth factor (PDGF)-BB, and insulin-like growth factor (IGF) II are added in combination along with retinoic acid, bFGF, TGF-beta 2, and TGF-beta 3. Also, these treatments induce N+,(+)-ATPase expression. When the QCE-6 cells are cultured on collagen type I, the mesenchymal cells that are promoted by retinoic acid, bFGF, TGF-beta 2, and TGF-beta 3 will invade the gel. These mesenchymal cells are positive for QH1 and JB3, which are both markers for presumptive endocardial cells within the early cardiogenic mesoderm. The addition of both PDGF-BB and IGF II to QCE-6 cell cultures will inhibit the ability of retinoic acid, bFGF, TGF-beta 2, and TGF-beta 3 to induce both the mesenchymal morphology and QH1 and JB3 expression. Collectively, these results suggest that the process of cardiac cell differentiation is regulated by multiple signals and that early cardiogenic mesoderm contains a bipotential stem cell that can give rise to both the myocardial and endocardial lineages. More important, since the QCE-6 cells are representative of early cardiogenic cells, this cell line offers a unique model system to study cardiac cell differentiation.
引用
收藏
页码:205 / 216
页数:12
相关论文
共 75 条
[21]  
FAMBROUGH DM, 1983, J BIOL CHEM, V258, P3926
[22]   CONGENITAL HEART-DISEASE - PREVALENCE AT LIVEBIRTH - THE BALTIMORE WASHINGTON INFANT STUDY [J].
FERENCZ, C ;
RUBIN, JD ;
MCCARTER, RJ ;
BRENNER, JI ;
NEILL, CA ;
PERRY, LW ;
HEPNER, SI ;
DOWNING, JW .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1985, 121 (01) :31-36
[23]   MONOCLONAL-ANTIBODIES TO DESMIN - EVIDENCE FOR STAGE-DEPENDENT INTERMEDIATE FILAMENT IMMUNOREACTIVITY DURING CARDIAC AND SKELETAL-MUSCLE DEVELOPMENT [J].
FISCHMAN, DA ;
DANTO, SI .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1985, 455 :167-184
[24]  
Gartside CL, 1991, DEV REGENERATION POT, P385
[25]   INVITRO ANALYSIS OF CARDIAC PROGENITOR-CELL DIFFERENTIATION [J].
GONZALEZSANCHEZ, A ;
BADER, D .
DEVELOPMENTAL BIOLOGY, 1990, 139 (01) :197-209
[26]   A SERIES OF NORMAL STAGES IN THE DEVELOPMENT OF THE CHICK EMBRYO [J].
HAMBURGER, V ;
HAMILTON, HL .
JOURNAL OF MORPHOLOGY, 1951, 88 (01) :49-&
[27]   EXPRESSION OF SARCOMERIC MYOSIN IN THE PRESUMPTIVE MYOCARDIUM OF CHICKEN EMBRYOS OCCURS WITHIN 6 HOURS OF MYOCYTE COMMITMENT [J].
HAN, Y ;
DENNIS, JE ;
COHENGOULD, L ;
BADER, DM ;
FISCHMAN, DA .
DEVELOPMENTAL DYNAMICS, 1992, 193 (03) :257-265
[28]   CELL-TRANSFORMATION BY CHEMICAL-AGENTS - A REVIEW AND ANALYSIS OF THE LITERATURE - A REPORT OF THE UNITED-STATES-ENVIRONMENTAL-PROTECTION-AGENCY GENE-TOX PROGRAM [J].
HEIDELBERGER, C ;
FREEMAN, AE ;
PIENTA, RJ ;
SIVAK, A ;
BERTRAM, JS ;
CASTO, BC ;
DUNKEL, VC ;
FRANCIS, MW ;
KAKUNAGA, T ;
LITTLE, JB ;
SCHECHTMAN, LM .
MUTATION RESEARCH, 1983, 114 (03) :283-385
[29]  
HEINE UI, 1985, VIRCHOWS ARCH B, V50, P135
[30]   MORPHOLOGICAL, BIOCHEMICAL, AND ELECTROPHYSIOLOGICAL CHARACTERIZATION OF A CLONAL CELL (H9C2) LINE FROM RAT-HEART [J].
HESCHELER, J ;
MEYER, R ;
PLANT, S ;
KRAUTWURST, D ;
ROSENTHAL, W ;
SCHULTZ, G .
CIRCULATION RESEARCH, 1991, 69 (06) :1476-1486