Journal article
Efficiently specified ventral midbrain dopamine neurons from human pluripotent stem cells under Xeno-free conditions restore motor deficits in Parkinsonian rodents
JC Niclis, CW Gantner, WF Alsanie, SJ McDougall, CR Bye, AG Elefanty, EG Stanley, JM Haynes, CW Pouton, LH Thompson, CL Parish
Stem Cells Translational Medicine | Published : 2017
Abstract
Recent studies have shown evidence for the functional integration of human pluripotent stem cell (hPSC)-derived ventral midbrain dopamine (vmDA) neurons in animal models of Parkinson’s disease. Although these cells present a sustainable alternative to fetal mesencephalic grafts, a number of hurdles require attention prior to clinical translation. These include the persistent use of xenogeneic reagents and challenges associated with scalability and storage of differentiated cells. In this study, we describe the first fully defined feeder- and xenogeneic-free protocol for the generation of vmDA neurons from hPSCs and utilize two novel reporter knock-in lines (LMX1A-eGFP and PITX3-eGFP) for in-..
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Funding Acknowledgements
We thank Ms. Mong Tien for assistance with perfusions and immunohistochemistry, as well as Ms. Haoyao Guo for whole cell recordings. This research was supported by funding from Stem Cells Australia. C.R.B. was supported by a National Health and Medical Research Council (NHMRC) Early Career Research Fellowship, and C.L.P. was supported by a Viertel Senior Medical Research Fellowship, Australia. A.G.E. and E.G.S. are senior research fellows of the NHMRC.