Human neural progenitor cells over-expressing IGF-1 protect dopamine neurons and restore function in a rat model of Parkinson's disease

2008 ◽  
Vol 209 (1) ◽  
pp. 213-223 ◽  
Author(s):  
Allison D. Ebert ◽  
Amy J. Beres ◽  
Amelia E. Barber ◽  
Clive N. Svendsen
2018 ◽  
Vol 7 (11) ◽  
pp. 829-838 ◽  
Author(s):  
Bárbara Mendes-Pinheiro ◽  
Fábio G. Teixeira ◽  
Sandra I. Anjo ◽  
Bruno Manadas ◽  
Leo A. Behie ◽  
...  

2018 ◽  
Vol 28 (3) ◽  
pp. 269-285 ◽  
Author(s):  
I. Madrazo ◽  
O. Kopyov ◽  
M. A. Ávila-Rodríguez ◽  
F. Ostrosky ◽  
H. Carrasco ◽  
...  

Individuals with Parkinson’s disease (PD) suffer from motor and mental disturbances due to degeneration of dopaminergic and non-dopaminergic neuronal systems. Although they provide temporary symptom relief, current treatments fail to control motor and non-motor alterations or to arrest disease progression. Aiming to explore safety and possible motor and neuropsychological benefits of a novel strategy to improve the PD condition, a case series study was designed for brain grafting of human neural progenitor cells (NPCs) to a group of eight patients with moderate PD. A NPC line, expressing Oct-4 and Sox-2, was manufactured and characterized. Using stereotactic surgery, NPC suspensions were bilaterally injected into patients’ dorsal putamina. Cyclosporine A was given for 10 days prior to surgery and continued for 1 month thereafter. Neurological, neuropsychological, and brain imaging evaluations were performed pre-operatively, 1, 2, and 4 years post-surgery. Seven of eight patients have completed 4-year follow-up. The procedure proved to be safe, with no immune responses against the transplant, and no adverse effects. One year after cell grafting, all but one of the seven patients completing the study showed various degrees of motor improvement, and five of them showed better response to medication. PET imaging showed a trend toward enhanced midbrain dopaminergic activity. By their 4-year evaluation, improvements somewhat decreased but remained better than at baseline. Neuropsychological changes were minor, if at all. The intervention appears to be safe. At 4 years post-transplantation we report that undifferentiated NPCs can be delivered safely by stereotaxis to both putamina of patients with PD without causing adverse effects. In 6/7 patients in OFF condition improvement in UPDRS III was observed. PET functional scans suggest enhanced putaminal dopaminergic neurotransmission that could correlate with improved motor function, and better response to L-DOPA. Patients’ neuropsychological scores were unaffected by grafting. Trial Registration: Fetal derived stem cells for Parkinson’s disease https://doi.org/10.1186/ISRCTN39104513Reg#ISRCTN39104513


2005 ◽  
Vol 16 (4) ◽  
pp. 509-521 ◽  
Author(s):  
Sandra M. Klein ◽  
Soshana Behrstock ◽  
Jacalyn McHugh ◽  
Kristin Hoffmann ◽  
Kyle Wallace ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-10 ◽  
Author(s):  
Parinya Noisa ◽  
Taneli Raivio ◽  
Wei Cui

Human embryonic stem cells (hESCs) are able to proliferatein vitroindefinitely without losing their ability to differentiate into multiple cell types upon exposure to appropriate signals. Particularly, the ability of hESCs to differentiate into neuronal subtypes is fundamental to develop cell-based therapies for several neurodegenerative disorders, such as Alzheimer’s disease, Huntington’s disease, and Parkinson’s disease. In this study, we differentiated hESCs to dopaminergic neurons via an intermediate stage, neural progenitor cells (NPCs). hESCs were induced to neural progenitor cells by Dorsomorphin, a small molecule that inhibits BMP signalling. The resulting neural progenitor cells exhibited neural bipolarity with high expression of neural progenitor genes and possessed multipotential differentiation ability. CBF1 and bFGF responsiveness of these hES-NP cells suggested their similarity to embryonic neural progenitor cells. A substantial number of dopaminergic neurons were derived from hES-NP cells upon supplementation of FGF8 and SHH, key dopaminergic neuron inducers. Importantly, multiple markers of midbrain neurons were detected, includingNURR1, PITX3, andEN1, suggesting that hESC-derived dopaminergic neurons attained the midbrain identity. Altogether, this work underscored the generation of neural progenitor cells that retain the properties of embryonic neural progenitor cells. These cells will serve as an unlimited source for the derivation of dopaminergic neurons, which might be applicable for treating patients with Parkinson’s disease.


PLoS ONE ◽  
2007 ◽  
Vol 2 (8) ◽  
pp. e689 ◽  
Author(s):  
Masatoshi Suzuki ◽  
Jacalyn McHugh ◽  
Craig Tork ◽  
Brandon Shelley ◽  
Sandra M. Klein ◽  
...  

2017 ◽  
Vol 26 (11) ◽  
pp. 1811-1821 ◽  
Author(s):  
Ruslan L. Nuryyev ◽  
Toni L. Uhlendorf ◽  
Wesley Tierney ◽  
Suren Zatikyan ◽  
Oleg Kopyov ◽  
...  

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