Persistent Dopamine Functions of Neurons Derived from Embryonic Stem Cells in a Rodent Model of Parkinson Disease

Author:

Rodríguez-Gómez Jose A.1,Lu Jian-Qiang2,Velasco Iván1,Rivera Seth3,Zoghbi Sami S.2,Liow Jeih-San2,Musachio John L.2,Chin Frederick T.2,Toyama Hiroshi2,Seidel Jurgen4,Green Michael V.4,Thanos Panayotis K.35,Ichise Masanori2,Pike Victor W.2,Innis Robert B.2,McKay Ron D. G.1

Affiliation:

1. Laboratory of Molecular Biology, National Institute of Neurological Disorders and Stroke, Porter Neuroscience Research Center, National Institutes of Health, Bethesda, Maryland, USA

2. Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, USA

3. Medical Department, Brookhaven National Laboratory, Upton, New York, USA

4. Clinical Center, National Institutes of Health, Bethesda, Maryland, USA

5. Laboratory of Neuroimaging, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland, USA

Abstract

Abstract The derivation of dopamine neurons is one of the best examples of the clinical potential of embryonic stem (ES) cells, but the long-term function of the grafted neurons has not been established. Here, we show that, after transplantation into an animal model, neurons derived from mouse ES cells survived for over 32 weeks, maintained midbrain markers, and had sustained behavioral effects. Microdialysis in grafted animals showed that dopamine (DA) release was induced by depolarization and pharmacological stimulants. Positron emission tomography measured the expression of presynaptic dopamine transporters in the graft and also showed that the number of postsynaptic DA D2 receptors was normalized in the host striatum. These data suggest that ES cell-derived neurons show DA release and reuptake and stimulate appropriate postsynaptic responses for long periods after implantation. This work supports continued interest in ES cells as a source of functional DA neurons. Disclosure of potential conflicts of interest is found at the end of this article.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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