DNA Methylation and Histone Acetylation Patterns in Cultured Bovine Adipose Tissue-Derived Stem Cells (BADSCs)

被引:0
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作者
Abouhamzeh, Beheshteh [1 ,2 ]
Salehi, Mohammad [1 ,3 ]
Hosseini, Ahmad [1 ]
Masteri-Farahani, Ali Reza [2 ]
Fadai, Fatemeh [2 ]
Heidari, Mohammad Hasan [2 ]
Nourozian, Mohsen [2 ]
Soleimani, Masoud [4 ]
Khorashadizadeh, Mohsen [5 ]
Mossahebi-Mohammadi, Majid [6 ]
Mansouri, Ardalan [1 ]
机构
[1] Shahid Beheshti Univ Med Sci, Cellular & Mol Biol Res Ctr, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Fac Med, Dept Cell Biol & Anat Sci, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Fac Med, Dept Biotechnol, Tehran, Iran
[4] Tarbiat Modares Univ, Fac Med Sci, Dept Hematol, Tehran, Iran
[5] Univ Tehran Med Sci, Sch Adv Med Technol, Dept Med Biotechnol, Tehran, Iran
[6] Stem Cell Technol Res Ctr, Dept Stem Cell Biol, Tehran, Iran
关键词
Somatic Cell Nuclear Transfer; Epigenetics; DNA Methyltransferases; Histone; Deacetyltransferses; NUCLEAR TRANSFER; MOUSE; EXPRESSION; PROTEINS; HYPOMETHYLATION; DIFFERENTIATION; PLURIPOTENCY; FIBROBLASTS; PROMOTERS; DISTINCT;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: Many studies have focused on the epigenetic characteristics of donor cells to improve somatic cell nuclear transfer (SCNT). We hypothesized that the epigenetic status and chromatin structure of undifferentiated bovine adipose tissue-derived stem cells (BADSCs) would not remain constant during different passages. The objective of this study was to determine the mRNA expression patterns of DNA methyltransferases (DNMT1, DNMT3a, DNMT3b) and histone deacetyltransferses (HDAC1, HDAC2, HDAC3) in BADSCs. In addition, we compared the measured levels of octamer binding protein-4 expression (OCT4) and acetylation of H3K9 (H3K9ac) in BADSCs cultures and different passages in vitro. Materials and Methods: In this experimental study, subcutaneous fat was obtained from adult cows immediately post-mortem. Relative level of DNMTs and HDACs was examined using quantitative real time polymerase chain reaction (q-PCR), and the level of OCT4 and H3K9ac was analyzed by flow cytometry at passages 3 (P3), 5 (P5) and 7 (P7). Results: The OCT4 protein level was similar at P3 and P5 but a significant decrease in its level was seen at P7. The highest and lowest levels of H3K9ac were observed at P5 and P7, respectively. At P5, the expression of HDACs and DNMTs was significantly decreased. In contrast, a remarkable increase in the expression of DNMTs was observed at P7. Conclusion: Our data demonstrated that the epigenetic status of BADSCs was variable during culture. The P5 cells showed the highest level of sternness and multipotency and the lowest level of chromatin compaction. Therefore, we suggest that P5 cells may be more efficient for SCNT compared with other passages.
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页码:466 / 475
页数:10
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