Substantial variation in the cardiac differentiation of human embryonic stem cell lines derived and propagated under the same conditionsa comparison of multiple cell lines

被引:48
作者
Pekkanen-Mattila, Mari [1 ,2 ]
Kerkela, Erja [1 ,2 ]
Tanskanen, Jarno M. A. [3 ]
Pietila, Mika [1 ,2 ]
Pelto-Huikko, Markku [4 ]
Hyttinen, Jari [3 ]
Skottman, Heli [1 ,2 ]
Suuronen, Riitta [1 ,2 ,3 ,5 ]
Aalto-Setala, Katriina [1 ,2 ,6 ]
机构
[1] Univ Tampere, Inst Regenerat Med, REGEA, Tampere 33520, Finland
[2] Tampere Univ Hosp, Tampere, Finland
[3] Tampere Univ Technol, Dept Biomed Engn, FIN-33101 Tampere, Finland
[4] Univ Tampere, Dept Dev Biol, Tampere 33520, Finland
[5] Tampere Univ Hosp, Dept Eye Ear & Oral Dis, Tampere, Finland
[6] Tampere Univ Hosp, Ctr Heart, Tampere, Finland
基金
芬兰科学院;
关键词
Cardiac; differentiation; gene expression; human embryonic stem cells; SERUM REPLACEMENT MEDIUM; CARDIOMYOCYTE DIFFERENTIATION; HUMAN BLASTOCYSTS; FEEDER CELLS; CULTURE; FIBROBLASTS; EXPRESSION; DERIVATION; MYOCYTES; HEART;
D O I
10.1080/07853890802609542
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim. The differentiation efficiencies of human embryonic stem cell (hESC) lines differ from each other. To assess this in more detail we studied the cardiac differentiation of eight hESC lines derived in the same laboratory. Results. Substantial variation in growth and in the ability to form beating areas was seen between the different hESC lines; line HS346 gave the best efficiency (9.4%), while HS293 did not differentiate into beating colonies at all. Nine germ layer and differentiation markers were quantified during early differentiation in four hESC lines. The expression levels of Brachyury T, MESP1 and NKX2.5 were highest in the most efficient cardiac line (HS346). A systematic characterization of the beating cells revealed proper cardiac marker expression, electrophysiological activity, and pharmacological response. Conclusions. The hESC lines derived in the same laboratory varied considerably in their potential to differentiate into beating cardiomyocytes. None of the expression markers could clearly predict cardiac differentiation potential, although the expression of early cardiomyogenic genes was upregulated in the best cardiac line. The proper cardiomyocyte characteristics and pharmacological response indicate that these cells could be used as a model for human cardiomyocytes in pharmacological and toxicological analyses when investigating new heart medications or cardiac side-effects.
引用
收藏
页码:360 / U17
页数:15
相关论文
共 38 条
[1]   Characterization of human embryonic stem cell lines by the International Stem Cell Initiative [J].
Adewumi, Oluseun ;
Aflatoonian, Behrouz ;
Ahrlund-Richter, Lars ;
Amit, Michal ;
Andrews, Peter W. ;
Beighton, Gemma ;
Bello, Paul A. ;
Benvenisty, Nissim ;
Berry, Lorraine S. ;
Bevan, Simon ;
Blum, Barak ;
Brooking, Justin ;
Chen, Kevin G. ;
Choo, Andre B. H. ;
Churchill, Gary A. ;
Corbel, Marie ;
Damjanov, Ivan ;
Draper, Jon S. ;
Dvorak, Petr ;
Emanuelsson, Katarina ;
Fleck, Roland A. ;
Ford, Angela ;
Gertow, Karin ;
Gertsenstein, Marina ;
Gokhale, Paul J. ;
Hamilton, Rebecca S. ;
Hampl, Ales ;
Healy, Lyn E. ;
Hovatta, Outi ;
Hyllner, Johan ;
Imreh, Marta P. ;
Itskovitz-Eldor, Joseph ;
Jackson, Jamie ;
Johnson, Jacqueline L. ;
Jones, Mark ;
Kee, Kehkooi ;
King, Benjamin L. ;
Knowles, Barbara B. ;
Lako, Majlinda ;
Lebrin, Franck ;
Mallon, Barbara S. ;
Manning, Daisy ;
Mayshar, Yoav ;
Mckay, Ronald D. G. ;
Michalska, Anna E. ;
Mikkola, Milla ;
Mileikovsky, Masha ;
Minger, Stephen L. ;
Moore, Harry D. ;
Mummery, Christine L. .
NATURE BIOTECHNOLOGY, 2007, 25 (07) :803-816
[2]   Differences between human embryonic stem cell lines [J].
Allegrucci, C. ;
Young, L. E. .
HUMAN REPRODUCTION UPDATE, 2007, 13 (02) :103-120
[3]   Genome-wide transcriptional profiling of human embryonic stem cells differentiating to cardiomyocytes [J].
Beqqali, Abdelaziz ;
Kloots, Jantine ;
Ward-van Oostwaard, Dorien ;
Mummery, Christine ;
Passier, Robert .
STEM CELLS, 2006, 24 (08) :1956-1967
[4]   Improved human embryonic stem cell embryoid body homogeneity and cardiomyocyte differentiation from a novel V-96 plate aggregation system highlights interline variability [J].
Burridge, Paul W. ;
Anderson, David ;
Priddle, Helen ;
Munoz, Maria D. Barbadillo ;
Chamberlain, Sarah ;
Allegrucci, Cinzia ;
Young, Lorraine E. ;
Denning, Chris .
STEM CELLS, 2007, 25 (04) :929-938
[5]   Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart [J].
Cai, CL ;
Liang, XQ ;
Shi, YQ ;
Chu, PH ;
Pfaff, SL ;
Chen, J ;
Evans, S .
DEVELOPMENTAL CELL, 2003, 5 (06) :877-889
[6]  
Cowan CA, 2004, NEW ENGL J MED, V350, P1353, DOI 10.1056/NEJMsr040330
[7]   Common culture conditions for maintenance and cardiomyocyte differentiation of the human embryonic stem cell lines, BG01 and HUES-7 [J].
Denning, C ;
Allegrucci, C ;
Priddle, H ;
Barbadillo-Muñoz, MD ;
Anderson, D ;
Self, T ;
Smith, NM ;
Parkin, CT ;
Young, LE .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 2006, 50 (01) :27-37
[8]   Mesenchymal stem cells are capable of homing to the bone marrow of non-human primates following systemic infusion [J].
Devine, SM ;
Bartholomew, AM ;
Mahmud, N ;
Nelson, M ;
Patil, S ;
Hardy, W ;
Sturgeon, C ;
Hewett, T ;
Chung, T ;
Stock, W ;
Sher, D ;
Weissman, S ;
Ferrer, K ;
Mosca, J ;
Deans, R ;
Moseley, A ;
Hoffman, R .
EXPERIMENTAL HEMATOLOGY, 2001, 29 (02) :244-255
[9]   Regulation of cardiomyocyte differentiation of embryonic stem cells by extracellular signalling [J].
Filipczyk, A. A. ;
Passier, R. ;
Rochat, A. ;
Mummery, C. L. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2007, 64 (06) :704-718
[10]   Enhanced cardiomyogenesis of human embryonic stem cells by a small molecular inhibitor of p38 MAPK [J].
Graichen, Ralph ;
Xu, Xiuqin ;
Braam, Stefan R. ;
Balakrishnan, Thavamalar ;
Norfiza, Siti ;
Sieh, Shirly ;
Soo, Set Yen ;
Tham, Su Chin ;
Mummery, Christine ;
Colman, Alan ;
Zweigerdt, Robert ;
Davidson, Bruce P. .
DIFFERENTIATION, 2008, 76 (04) :357-370