Differentiating HSPCs undergo progressive loss of differentiation capability in response to environmental conditions, resulting in terminally differentiated blood cells.
Here, we hypothesize that HDPSC may have pluripotent differentiation capability, and may be able to differentiate into skin epithelial keratinocytes in culture using organotypic 3D models based on the interaction with the subjacent dermal fibroblasts.
Moreover, MAPCs have been proven to be capable of extensive in vitro proliferation with no senescence or loss of differentiation capability.
Multipotent adult progenitor cells (MAPCs) are thought to be a more primitive stem cell population capable of extensive in vitro proliferation with no senescence or loss of differentiation capability.
The main advantage of it is its high order differentiation capability.
Damping ratio had marginally better differentiation capability than the damping coefficient.
We previously reported on human minor salivary gland mesenchymal stem cells (hMSGMSCs), which are highly self-renewable with multi-potent differentiation capability.
To evaluate the effect of a 17.5% H2O2 gel on the odontoblastic differentiation capability of human dental pulp cells (HDPCs).
We demonstrated that the chondrogenic differentiation capability of the BMDMSCs was improved by the addition of b-FGF.
However, the epithelial differentiation capability and the heterogeneity of these cells have not been fully explored to the date.
Differentiation capability of the DPSCs in the scaffolds was analyzed by measurement of the levels of calcified tissue formation and ALP activity.
