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Table 1 Selection of hiPSC lines regarding their expansion compatibility and cardiac differentiation efficiency in MC cultures. (A) Measurement of the highest flow cytometry population percentage of NKX2-5, Troponin T, MLC2a, CD44 and HNF4a on day 14 with a 24 h CHIR99021 induction of 4–14 μM on 5 cell lines in a monolayer attachment culture (n = 3). (B) Effects of continuous stirring on cell lines in MC-based spinner flask cultures. Cell yield, aggregate size and the expression of pluripotent (Oct4a and Tra-1-60) were measured (n = 3). (C) Selection of the best cell line for the cardiac differentiation on MC in a stirred spinner. Cell yield and the expression of cardiac marker Troponin T were measured (n = 3)

From: Selection of human induced pluripotent stem cells lines optimization of cardiomyocytes differentiation in an integrated suspension microcarrier bioreactor

 

DF6

CB6

BM1

IMR90

FR202

(A) Cardiac differentiation efficiency with CHIR99021 in MNL cultures (Maximum flow cytometry population expression at 4-14 μM CHIR99021 on day14)

NKX2–5 (%)

21.8 ± 17.1

1.7 ± 0.1

78.8 ± 25.5

82.9 ± 8.4

57.1 ± 7.2

Troponin T (%)

29.7 ± 24.6

2.1 ± 0.4

81.0 ± 31.2

83.1 ± 8.9

80.6 ± 2.1

MLC2a (%)

34.9 ± 25.7

1.95 ± 0.3

70.4 ± 21.9

64.9 ± 0.1

64.9 ± 9.4

CD44 (%)

40.5 ± 9.2

32.1 ± 8.4

16.5 ± 11.7

37.1 ± 14.9

3.7 ± 3.7

HNF4a (%)

38.8 ± 14.8

7.4 ± 1.9

13.6 ± 1.5

20.7 ± 5.9

4.4 ± 4.4

(B) Cell growth on MC in stirred spinner cultures (day 6)

Cells/mL (×106)

 

No cell growth

1.7 ± 0.3

1.9 ± 0.6

Expansion fold

14.0 ± 0.2

16.0 ± 0.5

Aggregate size (mm2)

0.42 ± 0.1

0.30 ± 0.1

Oct4a

94.3 ± 1.1

91.0 ± 0.1

Tra-1-60

93.0 ± 0.01

96.4 ± 0.1

(C) Cardiac differentiation on MC in stirred spinner cultures (day 12 of differentiation)

Cells/mL (×106)

 

2.1 ± 0.4

2.3 ± 0.2

Troponin T (%)

14.4 ± 8.5

83.2 ± 0.13

CM yields (cells/mL × 106)

0.32 ± 0.2

1.9 ± 0.03