Department of Cardiology, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Bengbu Medical School, Anhui Province, China.
J Cell Mol Med. 2019 Jan;23(1):104-111. doi: 10.1111/jcmm.13889. Epub 2018 Nov 5.
Bmi-1 gene is well recognized as an oncogene, but has been recently demonstrated to play a role in the self-renewal of tissue-specific stem cells. By using Bmi-1 mice, we investigated the role of Bmi-1 in cardiac stem/progenitor cells and myocardial repair. RT-PCR and flow cytometry analysis indicated that the expression of Bmi-1 was significantly higher in cardiac side population than the main population from CD45 Ter119 CD31 heart cells. More Sca-1 cardiac stem/progenitor cells were found in Bmi-1 GFP subpopulation, and these Bmi-1 GFP heart cells showed the potential of differentiation into SMM smooth muscle-like cells and TnT cardiomyocyte-like cells in vitro. The silencing of Bmi-1 significantly inhibited the proliferation and differentiation of heart cells. Otherwise, myocardial infarction induced a significantly increase (2.7-folds) of Bmi-1 GFP population, mainly within the infarction and border zones. These preliminary data suggest that Bmi-1 heart cells are enriched in cardiac stem/progenitor cells and may play a role in myocardial repair.
Bmi-1 基因被公认为癌基因,但最近有研究表明其在组织特异性干细胞的自我更新中发挥作用。我们通过使用 Bmi-1 小鼠,研究了 Bmi-1 在心脏干细胞/祖细胞和心肌修复中的作用。RT-PCR 和流式细胞术分析表明,在心脏侧群细胞中,Bmi-1 的表达明显高于 CD45 Ter119 CD31 心脏细胞中的主群细胞。在 Bmi-1 GFP 亚群中发现了更多的 Sca-1 心脏干细胞/祖细胞,这些 Bmi-1 GFP 心脏细胞在体外显示出分化为 SMM 平滑肌样细胞和 TnT 心肌细胞样细胞的潜能。Bmi-1 的沉默显著抑制了心脏细胞的增殖和分化。相反,心肌梗死导致 Bmi-1 GFP 群体显著增加(2.7 倍),主要在梗死区和边缘区。这些初步数据表明,Bmi-1 心脏细胞富含心脏干细胞/祖细胞,并可能在心肌修复中发挥作用。