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Background: Skin-derived
precursors (SKPs) are a type of progenitor cells extracted from mammalian
dermal tissue and can be differentiate to neural and mesodermal lineage in
vitro. These cells can introduce an accessible autologos source of neural precursor
cells for treatment of different neurodegenerative diseases. This research was done in order to set up isolation, culture,
proliferation and differentiation of human skin derived precursors (hSKPs).
Methods: Human foreskin
samples were cut into smaller pieces and cultured in proliferation medium after
enzymatic digestion. To induce neural differentiation, cells were cultured in
neural differentiation medium after fifth passage. We used immunocytochemistry
and RT-PCR for characterization of the cells. Neuron and glial
cell differentiation potential was assessed by immunofloresence using specific
antibodies. The experiments were carried out in triplicate.
Results: After
differentiation, βΙΙΙ- tubulin and neurofilament-M positive cells
were observed that are specific markers for neurons. Moreover, glial fibrillary acid protein (GFAP) and S100 positive cells were identified that are markers
specifically express in glial cells. Detected neurons and glials were also
confirmed by their morphologic characterizations.
Conclusion: Our results demonstrated that skin-derived precursors
obtained from human foreskin can exhibit neuronal and glial differentiation
potential in vitro, depending on the protocols of induction.
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