Title

Nanog Overexpression Increases Neural Marker Expression In Adipose Derived Stem Cells

Keywords

Adipose derived stem cells; Induced pluripotent stem cells; Nanog; Neural differentiation; Neural stem cells; Pluripotency

Abstract

Human neural stem cells (hNSCs) have shown potential in treating a variety of neurological diseases. However, they are impractical to isolate and use for an autologous transplant, generating demand for an alternative source of neural phenotypes. Utilizing our patented technology, adipose derived stem cells (ADSCs) may be a potential alternative source, as they are easily isolated and may have the potential to efficiently differentiate into neural phenotypes through transfection of the Nanog gene. ADSCs were transfected with a plasmid containing Nanog. Post-transfection, relative expression levels of Sox2, Oct4, and Nanog were assessed by qPCR. Transfected ADSCs were cocultured for 15 days with differentiated hNSCs using coculture inserts. Following coculture, levels of β-III-tubulin and glial fibrillary acidic protein (GFAP) were assessed by qPCR. Nanog transfected ADSCs expressed significantly increased levels of Nanog, Oct4, and Sox2 prior to coculture, indicating an increase in differentiation potential. Post-coculture, Nanog transfected ADSCs expressed significantly increased levels of β-III-tubulin and GFAP and spherical morphology, indicating an increased neural phenotype. These results demonstrate the effectiveness of our patented technology, suggesting that induced Nanog overexpression may provide a means to more readily generate neural phenotypes for use in transplantation based therapies. © 2014 Bentham Science Publishers.

Publication Date

1-1-2014

Publication Title

Recent Patents on Regenerative Medicine

Volume

4

Issue

1

Number of Pages

69-74

Document Type

Article

Personal Identifier

scopus

DOI Link

https://doi.org/10.2174/2210296504666140328221456

Socpus ID

84899874378 (Scopus)

Source API URL

https://api.elsevier.com/content/abstract/scopus_id/84899874378

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