TY - JOUR
T1 - Stem Cells Engineered During Different Stages of Reprogramming Reveal Varying Therapeutic Efficacies
AU - Bhere, Deepak
AU - Khajuria, Rajiv Kumar
AU - Hendriks, William T.
AU - Bandyopadhyay, Antara
AU - Bagci-Onder, Tugba
AU - Shah, Khalid
PY - 2018/6/1
Y1 - 2018/6/1
N2 - Stem cells are emerging as promising treatment strategies for several brain disorders and pathologies. In this study, we explored the potential of creating induced pluripotent stem cell-derived neural stem cells (ipNSC) by using either unmodified or gene-modified somatic cells and tested their fate and therapeutic efficacies in vitro and in vivo. We show that cells engineered in somatic state lose transgene-expression during the neural induction process, which is partially restored by histone deacetylase inhibitor treatment whereas cells engineered at the ipNSC state have sustained expression of transgenes. In vivo, bimodal mouse and human ipNSCs engineered to express tumor specific death-receptor ligand and suicide-inducing therapeutic proteins have profound anti-tumor efficacy when encapsulated in synthetic extracellular matrix and transplanted in mouse models of resected-glioblastoma. This study provides insights into using somatic cells for treating CNS disorders and presents a receptor-targeted cancer therapeutic approach for brain tumors. Stem Cells 2018;36:932–942.
AB - Stem cells are emerging as promising treatment strategies for several brain disorders and pathologies. In this study, we explored the potential of creating induced pluripotent stem cell-derived neural stem cells (ipNSC) by using either unmodified or gene-modified somatic cells and tested their fate and therapeutic efficacies in vitro and in vivo. We show that cells engineered in somatic state lose transgene-expression during the neural induction process, which is partially restored by histone deacetylase inhibitor treatment whereas cells engineered at the ipNSC state have sustained expression of transgenes. In vivo, bimodal mouse and human ipNSCs engineered to express tumor specific death-receptor ligand and suicide-inducing therapeutic proteins have profound anti-tumor efficacy when encapsulated in synthetic extracellular matrix and transplanted in mouse models of resected-glioblastoma. This study provides insights into using somatic cells for treating CNS disorders and presents a receptor-targeted cancer therapeutic approach for brain tumors. Stem Cells 2018;36:932–942.
UR - http://www.scopus.com/inward/record.url?scp=85044680354&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85044680354&partnerID=8YFLogxK
U2 - 10.1002/stem.2805
DO - 10.1002/stem.2805
M3 - Article
AN - SCOPUS:85044680354
SN - 1066-5099
VL - 36
SP - 932
EP - 942
JO - International Journal of Cell Cloning
JF - International Journal of Cell Cloning
IS - 6
ER -