4 weeks old male Sprague Dawley rats, weighing 100 - 120 grams were provided by the Institutional Experimental Animal Center of Shanxi medical university. Animal treatment corresponded to Management and use of laboratory Guide issued by US National Institutes of Health. The study protocol was reviewed and approved by the Institutional Animal Care and Use Committee.

Rats were executed by suffocation with carbon dioxide, and were then immersed in 75% alcohol for 5 minutes. Under the condition of no destroying rat thigh bone, two hind legs of the rat were dissected, and the fur, muscle and tendon of the legs were wiped out. Thigh bone was immersed in 75% alcohol for 3 minutes. It was then rinsed 2 times with PBS, and immersed in complete medium-LG-DMEM. The thigh bone was broken, and the marrow cavity was washed repeatedly 3 times with LG-DMEM. Slowly adding washing fluid which was obtained from marrow cavity as has been shown above on the surface of 5 ml Percoll Liquid Separation (1.077 g/ml), the mixture was centrifuged at centrifugal force of 1100 g/min for 30 minutes, and the stratum intermedium of mononuclear cells was sucked. The cells at the density of 2.5 × 10⁵ cells/cm² were inoculated in the culture plate which contained 10% Fetal Bovine Serum (FBS) and Low Glucose Dulbecco’s modified Eagle medium (LGDMEM). The cells above were cultured in the incubator which contained 5% CO₂ at 37˚C. Primary passage changed the medium at the fourth day, and then changed the culture medium every 3 days. When the attached cells got near confluence, they were digested by 0.25% pamcreatin-EDTA. The cells were transferred to culture at the ratio of 1:3 when passaged. The cell morphology was observed with Inverted phase contrast microscope (CKX 41, Olympus Company).

The second generation of BMSCs was digested by 0.25% pamcreatin-EDTA，cell density was adjusted to 3 × 10⁴ cells/ml, and the cells were inoculated in nine 96 well plates. 200 μl of cell suspension was added in each well. Got one of the plates every day after their adherence, and 20 μl MTT (5 mg/ml) was added into every well. The cells were incubated at ±37˚C for 4 hours, and supernatant in every well was then discarded. 150 μl DMSO was added into each well, then the plate was placed on the concentrator for 10 minutes at low-speed oscillation in order to dissolve the purple crystal sufficiently. The absorbance (OD) of each well was measured with ELISA apparatus (680, Bio-Rad) at 490 nm wavelength, the results were recorded, and the growth curve was drawn.

When the BMSCs had been passaged for second, sixth, or tenth generation, they were incubated by 5 μmol/L, 10 μmol/L, and 15 μmol/L 5-Aza for 24 hours respectively. The culture medium which contained 5-Aza was sucked. Then they were cultured for 4 weeks. Untreated cells acted as negative control group. Cell morphology were monitored by Inverted phase contrast microscope (CKX41, Olympus Company).

BMSCs at the second, sixth, and tenth generation were selected, and were inoculated in a 96 well plate at a cell density of 3 × 10⁴ cells/ml respectively. Three plates were inoculated for each generation. Each plate was divided into 4 groups, each group included 23 wells, and the remaining 4 wells were set up for zero holes. Three groups in every 96 well plate acted as induced groups, and 5 μmol/L, 10 μmol/L, 15 μmol/L 5-Aza was used to inoculate BMSCs for 24 hours respectively. 23 wells acted as a control group in every 96 well plate, and were inoculated in complete medium for 24 hours. All groups were then incubated with complete medium for 5 days. Absorbance (OD) was measured with MTT at the first, third and fifth day after being induced with 5-Aza.

BMSCs at the second, sixth and tenth generation were detected with Desmin after being induced with the different concentrations, i.e. 5 μmol/L, 10 μmol/L and 15 μmol/L 5-Aza for 4 weeks. The second generation BMSCs were detected with troponin T, α-Actin expression after being induced with 10 μmol/L 5-Aza for 4 weeks, The normal rat cardiomyocytes acted as a positive control group, and the untreated BMSCs acted as negative control group.

Cells that grown on labteck chamber slides (50 × 10⁴ cells/well) (Nunc) were washed with PBS (0.01 mmol/L, pH 7.4), fixed with 4% paraformaldehyde for 20 min and permeabilized with 0.1% Triton X-100/PBS (Sigma) for 15 min. Endogenous peroxidase was blocked with 3% H₂O₂—methanol for 15 min. Each manipulation was preceded by washing the cells three times in PBS with 0.05% Tween 20 (Sigma). After blocking in PBS-BSA 5% (Sigma) for 1 h, the cells were incubated overnight at 4˚C with the primary antibodies: Rabbit polyclonal to Desmin (Desmin, crossreactivity with mouse) 1:300, Shanghai Bluegene Biotech CO., LTD; Mouse antiRabbit cardiac Troponin T (cTnT, crossreactivity with mouse), 1:200, Sigma; Rabbit polyclonal to alpha smooth muscle Actin (α-Actin, crossreactivity with mouse), 1:300, Sigma. Bound primary antibodies were visualized by Peroxidase labeled streptomycin avidin staining reagents (Shanghai Bluegene Biotech CO., LTD). Slices were mounted, and were observed with Inverted microscope system (CKX 41, Olympus Company). The same protocols were followed for staining of the normal rat cardiomyocytes and the untreated BMSCs.

Total RNA was extracted from the second passage BMSCs which have been induced with 5-Aza for 4 weeks using Trizol reagent (Invitrogen, Carlsbad, CA). RNA samples were treated with Superscript III RNase H-reverse transcriptase (Invitrogen, Carlsbad, CA) to converting to cDNA in a 20 μL reaction mixture. The sequences of PCR primers for GATA-4, Nkx 2.5 and TDGF-l were as follows: GATA-4, 130 bp, 5’-GAC TGA GTT CTG GGC ATCT-3’ and 5’-CAA TCT TTA GGC TCT GGTTT-3’; Nkx 2.5, 102 bp, 5’-CGC CAA CAG CAA CTT CGT-3’ and 5’-ATG CCG TGC AGC GTG GAGAC-3’; TDGF-l, 183 bp, 5’-GCA ACT GTG AGC ACG ATG-3’ and 5’-GTG GAG TCC TGG ATA CCTT-3’. RNA of untreated third passage BMSCs was used as negative control. The PCR products were sizefractionated by 1% agarose gel electrophoresis.

Fresh adult bovine pericardium was collected and transported in ice brine protection. Residual fat and connective tissue was removed from the pericardial surface. The bovine pericardium was cut into pieces of 0.5 cm × 0.5 cm, put in 0.1% bromogeramine liquid for 30 minutes, then washed repeatedly with PBS to remove bromogeramine from the bovine surface. Acellular bovine pericardium was obtained by using the method of detergent-enzyme digestion [16], and it was crosslinked with 0.625% genipin solution (2 ml/cm²) for 72 hours. Then the acellular bovine pericardium was rinsed with PBS. It was placed on a Petri dish, thoroughly disinfected by ultraviolet light for 20 minutes, immersed in 75% alcohol for 30 minutes, and rinsed 3 times with PBS. After this procedure, it was placed in LG-DMEM for 6 hours before seeded by BMSCs.

After BMSCs at the third generation induced by 10 μmol/L 5-Aza had overgrown the 100 millimeter-sized culture dish, they were digested by 0.25% pancreatinEDTA, then centrifuged with 1500 rpm × 10 min. The supernatant was thrown away and the appropriate amount culture medium was added to form cell suspension. Cells with a density of 4.0 - 5.0 × 10⁶ cells/cm² were implanted on acellular bovine pericardium which had been treated with Poly-L-Lysine at a concentration of 2 mg/180 ml. After 4 hours incubation +37˚C, 5% CO₂, the sufficient cell culture medium was added, supplemented with 10 μmol/L Basic fibroblast growth factor (bFGF). The complex of cells and scaffold had been cultured for 2 weeks in the Incubator +37˚C, 5% CO₂. During this period, the culture medium was changed every two days. After it had been seeded for 2 weeks, histological detection was made.

The sample data was analyzed with SPSS 13.0. Data description was indicated with mean ± standard deviation (X ± SD). The difference among groups was analyzed with Analysis of variance (ANOVA). Comparison between two groups was tested with the student-Newman-Keuls (SNK) method. Test level is α = 0.05, and P < 0.05 is significant difference.

The BMSCs during the primary culture period looked like small, short spindle or triangular cells after they had been seeded in the complete medium for 48 hours, and the cells had a good refractional capability. The percoll particles could be seen on the surface of the cells. After they had been seeded for 72 hours, the BMSCs looked like slender spindle cells. From the fourth day, the BMSCs had a significant proliferation, companied with many double refraction bodies, and formed island-like clones. Cells were arranged irregularly when cell density was lower, and triangular cells could be seen. Cells formed 70% - 80% confluence at the seventh-tenth day, then began to arrange regularly, and appeared as bundle, whirlpool or fish-like shapes. BMSCs’ morphology tended to be a unanimous appearance when passaged to the second generation (Figure 1).

Some of the cells at every generation died after being induced with 5 μmol/L, 10 μmol/L or 15 μmol/L 5-Aza for 24 hours. Cell mortality was increased with higher 5-Aza concentration, but generations didn’t seem to have an influence on cell mortality. After being induced with 5-Aza for 24 hours, some of the adherent cells became flat or short rod shape. Cells began to proliferate after being induced for 3 days, some presented the slender spindle shape, and others appeared triangular or polygonnal. After being cultured for 4 weeks, 80% - 90% cells presented mainly with a myofiber shape, though a few looked polygonal or flagstone-like shape, and cells grew

in an aggregation-like method. No spontaneous beating cells could be observed for different generations of BMSCs or different concentrations of 5-Aza (Figure 2).

BMSCs subculture incubation period continued 1 or 2 days. By the third or fourth day, they had begun the logarithmic growth phase. At the sixth or seventh day, they entered into the platform period (Figure 3).

BMSCs at different generations induced with different concentrations of 5-Aza were detected with MTT. It has been demonstrated that the second generation BMSCs was superior to the sixth, and tenth generation in proliferation capacity after being induced, but there was no statistical difference between the sixth and tenth comparison. In the control group, having no induction with 5-Aza, the second and sixth generation BMSCs showed no statistical difference in proliferation capacity, but all were superior to the tenth generation. 5-Aza had some influence on proliferation capacity, but with the increase of generations, this influence had a weakening trend (Figures 4-6 and Tables 1 and 2).

BMSCs at the second, sixth and tenth generation were

detected with immunocytochemistry for Desmin after being induced with the different concentrations, i.e. 5 μmol/L, 10 μmol/L and 15 μmol/L 5-Aza for 4 weeks. Cells in all groups had positive expression for desmin. It was demonstrated that BMSCs at the second, sixth and tenth generation treated with the three different concentrations above had been induced and transformed to the myocardial orientation, and expressed cardiac-specific protein (Figure 7).

Table 1. The proliferation rate of the second, sixth and tenth BMSCs induced with the concentration 5-Aza for 5 days and control group BMSCs.

Note: ^*indicate P < 0.05 when compared with the second generation, ^△indicate P < 0.05 when compared with the 6th generation.

Table 2. The proliferation rate of the same passage BMSCs induced with the different concentration 5-Aza for 5 days and control group BMSCs.

Note: ^*indicate P < 0.05 when compared with the control group, ^△indicate P < 0.05 when compared with the group induced with 5 μmol 5-Aza.

After the second generation BMSCs being induced with 10 μmol/L 5-Aza for 4 weeks, the induced group, negative group and positive group were detected with immunocytochemistry for troponin T, α-Actin expression. BMSCs in the induced group and positive group showed expression, but BMSCs in the negative group had no expression. It was demonstrated that BMSCs treated with 5-Aza have been induced and transformed to the myocardial orientation, and expressed cardiac-specific protein (Figure 8).

The results of RT-PCR indicated that BMSCs induced with 5-Aza expressed GATA-4, Nkx 2.5 and TDGF-l. The induced group had an obvious stripe at 130 pb, 102 pb and 183 pb. It was demonstrated that BMSCs in the induced group had expressed the early myocardial forming transcription factor, such as GATA-4, Nkx 2.5, TDGF-l, etc., but none of in the control group (Figure 9).

Bovine pericardium after treatment with 0.625% genipin solution presented light blue. Its texture was flexible, and had a highly flexible character (Figure 10).

Induced BMSCs were attached on the surface of bovine pericardium, and the levels were distinctive. It was demonstrated that induced BMSCs could be attached on the surface of acellular bovine pericardium (Figure 11).