Abstrak 
Transplantation Of Feeder-free Human Induced Pluripotent Stem Cell–derived Cortical Neuron Progenitors In Adult Male Wistar Rats With Focal Brain Ischemia
Yulius Hermanto, Tadashi Sunohara, Ahmad Faried, Yasushi Takagi, Jun Takahashi, Takakuni Maki, Susumu Miyamoto
Universitas Padjadjaran, J NeuroRes. 2017;1–12, wileyonlinelibrary.com/journal/jnr, Wiley Periodicals, Inc., DOI 10.1002/hpm.2408
Bahasa Inggris
Universitas Padjadjaran, J NeuroRes. 2017;1–12, wileyonlinelibrary.com/journal/jnr, Wiley Periodicals, Inc., DOI 10.1002/hpm.2408
cell therapy, human pluripotent stem cells, Ischemic stroke, neural stem cells
The use of human induced pluripotent stem cells (hiPSCs) eliminates the ethical issues associated with fetal or embryonic materials, thus allowing progress in cell therapy research for ischemic stroke. Strict regulation of cell therapy development requires the xeno-free condition to eliminate clinical complications. Maintenance of hiPSCs with feeder-free condition presents a higher degree of spontaneous differentiation in comparison with conventional cultures. Therefore, feeder-free derivation might be not ideal for developing transplantable hiPSC derivatives. We developed the feeder-free condition for differentiation of cortical neurons from hiPSCs. Then, we evaluated the cells’ characteristics upon transplantation into the sham and focal brain ischemia on adult male Wistar rats. Grafts in lesioned brains demonstrated polarized reactivity toward the ischemic border, indicated by directional preferences in axonal outgrowth and cellular migration, with no influence on graft survival. Following the transplantation, forelimb asymmetry was better restored compared with controls. Herein, we provide evidence to support the use of the xeno-free condition for the development of cell therapy for ischemic stroke.