TY - JOUR
T1 - Effect of Octamer-Binding Transcription Factor 4 Overexpression on the Neural Induction of Human Dental Pulp Stem Cells
AU - Gancheva, Maria R.
AU - Kremer, Karlea
AU - Breen, James
AU - Arthur, Agnes
AU - Hamilton-Bruce, Anne
AU - Thomas, Paul
AU - Gronthos, Stan
AU - Koblar, Simon
N1 - Funding Information:
Open Access funding enabled and organized by CAUL and its Member Institutions This work was supported by The Hospital Research Foundation (2019-060-25252), Stroke SA Inc. (2016), and Rebecca L. Cooper Medical Research Foundation (2017).
Publisher Copyright:
© 2024, The Author(s).
PY - 2024/2/5
Y1 - 2024/2/5
N2 - Stem cell-based therapy is a potential alternative strategy for brain repair, with neural stem cells (NSC) presenting as the most promising candidates. Obtaining sufficient quantities of NSC for clinical applications is challenging, therefore alternative cell types, such as neural crest-derived dental pulp stem cells (DPSC), may be considered. Human DPSC possess neurogenic potential, exerting positive effects in the damaged brain through paracrine effects. However, a method for conversion of DPSC into NSC has yet to be developed. Here, overexpression of octamer-binding transcription factor 4 (OCT4) in combination with neural inductive conditions was used to reprogram human DPSC along the neural lineage. The reprogrammed DPSC demonstrated a neuronal-like phenotype, with increased expression levels of neural markers, limited capacity for sphere formation, and enhanced neuronal but not glial differentiation. Transcriptomic analysis further highlighted the expression of genes associated with neural and neuronal functions. In vivo analysis using a developmental avian model showed that implanted DPSC survived in the developing central nervous system and respond to endogenous signals, displaying neuronal phenotypes. Therefore, OCT4 enhances the neural potential of DPSC, which exhibited characteristics aligning with neuronal progenitors. This method can be used to standardise DPSC neural induction and provide an alternative source of neural cell types. Graphical Abstract: [Figure not available: see fulltext.].
AB - Stem cell-based therapy is a potential alternative strategy for brain repair, with neural stem cells (NSC) presenting as the most promising candidates. Obtaining sufficient quantities of NSC for clinical applications is challenging, therefore alternative cell types, such as neural crest-derived dental pulp stem cells (DPSC), may be considered. Human DPSC possess neurogenic potential, exerting positive effects in the damaged brain through paracrine effects. However, a method for conversion of DPSC into NSC has yet to be developed. Here, overexpression of octamer-binding transcription factor 4 (OCT4) in combination with neural inductive conditions was used to reprogram human DPSC along the neural lineage. The reprogrammed DPSC demonstrated a neuronal-like phenotype, with increased expression levels of neural markers, limited capacity for sphere formation, and enhanced neuronal but not glial differentiation. Transcriptomic analysis further highlighted the expression of genes associated with neural and neuronal functions. In vivo analysis using a developmental avian model showed that implanted DPSC survived in the developing central nervous system and respond to endogenous signals, displaying neuronal phenotypes. Therefore, OCT4 enhances the neural potential of DPSC, which exhibited characteristics aligning with neuronal progenitors. This method can be used to standardise DPSC neural induction and provide an alternative source of neural cell types. Graphical Abstract: [Figure not available: see fulltext.].
KW - Cell-based therapy
KW - Cellular reprogramming
KW - Dental pulp stem cells
KW - Neural
KW - Neuronal
KW - Octamer-binding transcription factor 4
UR - http://www.scopus.com/inward/record.url?scp=85184246352&partnerID=8YFLogxK
U2 - 10.1007/s12015-024-10678-7
DO - 10.1007/s12015-024-10678-7
M3 - Article
AN - SCOPUS:85184246352
SN - 2629-3269
JO - Stem Cell Reviews and Reports
JF - Stem Cell Reviews and Reports
ER -