Progenitor Cells Derived from Drain Waste Product of Open-Heart Surgery in Children.
Tak-Wah WongChung-Dann KanWen-Tai ChiuKin Lam FokYe Chun RuanXiaohua JiangJunjiang ChenChiu-Ching KaoI-Yu ChenHui-Chun LinChia-Hsuan ChouChou-Wen LinChun-Keung YuStephanie TsaoYi-Ping LeeHsiao Chang ChanJieh-Neng WangPublished in: Journal of clinical medicine (2019)
Human cardiac progenitor cells isolated from the same host may have advantages over other sources of stem cells. The aim of this study is to establish a new source of human progenitor cells collected from a waste product, pericardiac effusion fluid, after open-heart surgery in children with congenital heart diseases. The fluid was collected every 24 h for 2 days after surgery in 37 children. Mononuclear cells were isolated and expanded in vitro. These pericardial effusion-derived progenitor cells (PEPCs) exhibiting cardiogenic lineage markers, were highly proliferative and enhanced angiogenesis in vitro. Three weeks after stem cell transplantation into the ischemic heart in mice, cardiac ejection fraction was improved significantly without detectable progenitor cells. Gene expression profiles of the repaired hearts revealed activation of several known repair mechanisms including paracrine effects, cell migration, and angiogenesis. These progenitor cells may have the potential for heart regeneration.
Keyphrases
- endothelial cells
- minimally invasive
- stem cells
- stem cell transplantation
- ejection fraction
- heart failure
- cell migration
- young adults
- coronary artery bypass
- high dose
- left ventricular
- heavy metals
- vascular endothelial growth factor
- induced apoptosis
- single cell
- type diabetes
- oxidative stress
- ischemia reperfusion injury
- pluripotent stem cells
- gene expression
- skeletal muscle
- metabolic syndrome
- surgical site infection
- bone marrow
- blood brain barrier
- risk assessment
- copy number
- acute coronary syndrome
- insulin resistance
- mesenchymal stem cells
- endoplasmic reticulum stress
- pi k akt