Adult adipose stromal cells are accessible, numerous, show multipotent differentiation potential and low immunogenicity, and are not subjected to ethical issues. Additionally, they can be induced to differentiate into...Adult adipose stromal cells are accessible, numerous, show multipotent differentiation potential and low immunogenicity, and are not subjected to ethical issues. Additionally, they can be induced to differentiate into neuron-like cells and astrocytes in vitro through addition of β-mercaptoethanol and 0,5% anhydrous ethanol.展开更多
Previous in vivo experiments have shown that human umbilical cord blood mesenchymal stem cells can promote the proliferation and differentiation of damaged celts, and help to repair damaged sites, Recent studies have ...Previous in vivo experiments have shown that human umbilical cord blood mesenchymal stem cells can promote the proliferation and differentiation of damaged celts, and help to repair damaged sites, Recent studies have reported that umbilical cord blood-derived mesenchymal stem cells can differentiate into neurons and glial cells. Recent studies have reported that the repair mechanisms underlying cord blood stern cells involve the replacement of damaged cells and mediation of the local micro-environment.展开更多
文摘Adult adipose stromal cells are accessible, numerous, show multipotent differentiation potential and low immunogenicity, and are not subjected to ethical issues. Additionally, they can be induced to differentiate into neuron-like cells and astrocytes in vitro through addition of β-mercaptoethanol and 0,5% anhydrous ethanol.
文摘Previous in vivo experiments have shown that human umbilical cord blood mesenchymal stem cells can promote the proliferation and differentiation of damaged celts, and help to repair damaged sites, Recent studies have reported that umbilical cord blood-derived mesenchymal stem cells can differentiate into neurons and glial cells. Recent studies have reported that the repair mechanisms underlying cord blood stern cells involve the replacement of damaged cells and mediation of the local micro-environment.