Lois and Alvarez-Buylla, 1994
|
~100 μm diameter explants |
NSE-LacZ mice |
None |
Wild-type mice |
30 days |
No migration of surviving cells outside of transplantation site |
Herrera et al., 1999
|
~150 μm diameter explants |
NSE-LacZ mice |
None |
Mice with kainic acid lesions |
2, 4, 6, and 8 weeks |
Limited migration of transplanted cells Vast majority of surviving NSE-LacZ expressing cells were astrocytes |
Zhang et al., 2003
|
Dissociated cell suspensions |
Wild-type rat |
Neural progenitor cells cultured for 8 days in media with FGF2, horse and calf serum; cells were labeled with either BrdU or DiO |
Wild-type rats |
7 and 28 days |
Substantial migration away from transplantation site Majority of BrdU and DiO labeled cells expressed either MAP2 or NeuN, few expressed GFAP |
Meissner et al., 2005
|
Neurosphere suspensions |
βActin-CMV-GFP mice |
Neurospheres were cultured for 5 passages in the presence of EGF and FGF2 |
Mice with unilateral 6-hydroxydopamine OHDA lesions |
1 month |
Low survival rate of transplanted cells ~7% and ~2% of surviving cells expressed TH Improved motor performance to apomorphine and amphetamine challenges |
Richardson et al., 2005
|
Dissociated cell suspensions |
Wild-type rat |
Neural progenitor cells isolated by a Percoll gradient, cultured for 1 week in media containing FGF2, then 6 days in media containing retinoic acid without FGF2; cells were labeled with BrdU |
Rats with unilateral 6-hydroxydopamine OHDA lesions |
2 weeks |
Many surviving transplanted cells maintain Nestin expression, but none expressed NeuN Improved motor performance to amphetamine challenge |
Seidenfaden et al., 2006
|
~100 μm diameter explants |
βActin-CMV-GFP mice |
None |
Wild-type mice |
3 weeks and 6 months |
Limited migration and low survival rate of transplanted cells Most surviving cells expressed glial marker genes |
Chen et al., 2007b
|
Neurosphere suspensions |
Wild-type rat |
Neural progenitor cells isolated by a Percoll gradient protocol, cultured for 2 weeks in media containing EGF and FGF2; cells were labeled with BrdU |
Wild-type rat |
6 weeks |
Substantial migration away from transplantation site Most surviving cells expressed GFAP and none expressed NeuN |
Chen et al., 2007a
|
Neurosphere suspensions |
Wild-type rat |
Neural progenitor cells isolated by a Percoll gradient protocol, cultured for 2 weeks in media containing EGF and FGF2; cells were labeled with BrdU |
Rats transduced with AAV1/2 vectors to over-express either BDNF or FGF2 in the striatum |
6 and 12 weeks |
AAV1/2-FGF2 improved survival of transplanted cells Most surviving transplanted cells expressed glial marker genes AAV1/2-BDNF increased percentage of surviving cells expressing NeuN |
Shim et al., 2007
|
Dissociated cell suspensions |
Wild-type rat |
Neurospheres were cultured in media containing EGF, FGF2, and PDGF for over 2 months; retroviral transduction to over-express Nurr1 and Mash1 |
Rats with unilateral 6-hydroxydopamine OHDA lesions |
2, 4, and 6 weeks |
Substantial number of surviving transplanted cells expressed MAP2, TH and VMAT2 Improved motor performance to amphetamine challenge |
Deleidi et al., 2011
|
Dissociated cell suspensions |
rTA/Oct4 mice |
Neurospheres were expanded for 14 days before being converted to induced pluripotent stem cells and then differentiated via 5 stage protocol; SSEA1+ cells were removed by cell sorting prior to transplantation |
Rats with unilateral 6-hydroxydopamine OHDA lesions |
4, 6, and 8 weeks |
Substantial number of surviving transplanted cells express TH Improved motor performance to apomorphine and amphetamine challenges |