Bmi-1 high-expressing cells enrich cardiac stem/progenitor cells and respond to heart injury.
Yuewang SongMengmeng ZhaoYuan XieTingfang ZhuWenbin LiangBaiming SunWeixin LiuLiqun WuGuoping LuTao-Sheng LiTong YinYucai XiePublished in: Journal of cellular and molecular medicine (2018)
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-1GFP /+ 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 GFPhi subpopulation, and these Bmi-1 GFPhi 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 GFPhi population, mainly within the infarction and border zones. These preliminary data suggest that Bmi-1hi heart cells are enriched in cardiac stem/progenitor cells and may play a role in myocardial repair.
Keyphrases
- body mass index
- induced apoptosis
- left ventricular
- cell cycle arrest
- stem cells
- weight gain
- heart failure
- signaling pathway
- endoplasmic reticulum stress
- smooth muscle
- atrial fibrillation
- gene expression
- skeletal muscle
- high resolution
- big data
- metabolic syndrome
- adipose tissue
- angiotensin ii
- genome wide
- climate change
- artificial intelligence
- mass spectrometry
- insulin resistance
- weight loss
- bone marrow
- copy number
- diabetic rats