RRC ID 43660
Author Nishimura K, Nakagawa T, Sakamoto T, Ito J.
Title Fates of murine pluripotent stem cell-derived neural progenitors following transplantation into mouse cochleae.
Journal Cell Transplant
Abstract This study evaluated the tumorigenesis risk of induced pluripotent stem (iPS) cells after transplantation into the cochlea. One mouse embryonic stem (ES) cell line and three mouse iPS cell lines, one derived from adult mouse tail-tip fibroblasts (TTFs) and two from mouse embryonic fibroblasts (MEFs), were neurally induced by stromal cell-inducing activity. Before transplantation, the efficiency of neural induction and the proportion of residual undifferentiated cells were evaluated using immunocytochemistry, and no significant differences were observed in the ratios of colonies expressing βIII tubulin, nestin, or octamer (Oct)3/4. Four weeks after transplantation into the cochleae of neonatal mice, the number of surviving transplants of TTF-derived iPS cells generated by retroviral infection was significantly higher than those of MEF-derived iPS cells generated by plasmid transfection. Teratoma formation was identified in one of five cochleae transplanted with TTF-derived iPS cells. However, no significant differences were found in the cell proliferation activity or the extent of differentiation into mature neurons among the cell lines. These findings emphasize the necessity of selecting appropriate iPS cell lines and developing methods to eliminate undifferentiated cells after neural induction, in order to establish safe iPS cell-based therapy for the inner ear.
Volume 21(4)
Pages 763-71
Published 2012-1-1
DOI 10.3727/096368911X623907
PII ct0332nishimura
PMID 22305181
MeSH Animals Cell Differentiation / physiology Cochlea / cytology* Mice Mice, Inbred C57BL Neural Stem Cells / cytology* Pluripotent Stem Cells / cytology* Stem Cell Transplantation / adverse effects Teratoma / pathology
IF 3.341
Times Cited 29
Human and Animal Cells MC3T3-G2/PA6(RCB1127)