TY - JOUR
T1 - Directed differentiation of human induced pluripotent stem cells toward bone and cartilage
T2 - In vitro versus in vivo assays
AU - Phillips, Matthew D.
AU - Kuznetsov, Sergei A.
AU - Cherman, Natasha
AU - Park, Kyeyoon
AU - Chen, Kevin G.
AU - McClendon, Britney N.
AU - Hamilton, Rebecca S.
AU - McKay, Ronald D.G.
AU - Chenoweth, Josh G.
AU - Mallon, Barbara S.
AU - Robey, Pamela G.
PY - 2014
Y1 - 2014
N2 - The ability to differentiate induced pluripotent stem cells (iPSCs) into committed skeletal progenitors could allow for an unlimited autologous supply of such cells for therapeutic uses; therefore, we attempted to create novel bone-forming cells from human iPSCs using lines from two distinct tissue sources and methods of differentiation that we previously devised for osteogenic differentiation of human embryonic stem cells, and as suggested by other publications. The resulting cells were assayed using in vitro methods, and the results were compared with those obtained from in vivo transplantation assays. Our results show that true bone was formed in vivo by derivatives of several iPSC lines, but that the successful cell lines and differentiation methodologies were not predicted by the results of the in vitro assays. In addition, bone was formed equally well from iPSCs originating from skin or bone marrow stromal cells (also known as bone marrow-derived mesenchymal stem cells), suggesting that the iPSCs did not retain a "memory" of their previous life. Furthermore, one of the iPSC-derived cell lines formed verifiable cartilage in vivo, which likewise was not predicted by in vitro assays.
AB - The ability to differentiate induced pluripotent stem cells (iPSCs) into committed skeletal progenitors could allow for an unlimited autologous supply of such cells for therapeutic uses; therefore, we attempted to create novel bone-forming cells from human iPSCs using lines from two distinct tissue sources and methods of differentiation that we previously devised for osteogenic differentiation of human embryonic stem cells, and as suggested by other publications. The resulting cells were assayed using in vitro methods, and the results were compared with those obtained from in vivo transplantation assays. Our results show that true bone was formed in vivo by derivatives of several iPSC lines, but that the successful cell lines and differentiation methodologies were not predicted by the results of the in vitro assays. In addition, bone was formed equally well from iPSCs originating from skin or bone marrow stromal cells (also known as bone marrow-derived mesenchymal stem cells), suggesting that the iPSCs did not retain a "memory" of their previous life. Furthermore, one of the iPSC-derived cell lines formed verifiable cartilage in vivo, which likewise was not predicted by in vitro assays.
KW - Bone
KW - Chondrogenesis
KW - Induced pluripotent stem cells
KW - Osteoblast
KW - Transplantation
UR - http://www.scopus.com/inward/record.url?scp=84903518256&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84903518256&partnerID=8YFLogxK
U2 - 10.5966/sctm.2013-0154
DO - 10.5966/sctm.2013-0154
M3 - Article
C2 - 24855277
SN - 2157-6564
VL - 3
SP - 867
EP - 878
JO - Stem Cells Translational Medicine
JF - Stem Cells Translational Medicine
IS - 7
ER -