TY - JOUR
T1 - Directing dopaminergic fiber growth along a preformed molecular pathway from embryonic ventral mesencephalon transplants in the rat brain
AU - Jin, Y.
AU - Zhang, C.
AU - Ziemba, K. S.
AU - Goldstein, G. A.
AU - Sullivan, P. G.
AU - Smith, G. M.
PY - 2011/5
Y1 - 2011/5
N2 - To identify guidance molecules to promote long-distance growth of dopaminergic axons from transplanted embryonic ventral mesencephalon (VM) tissue, three pathways were created by expressing green fluorescent protein (GFP), glial cell line-derived neurotrophic factor (GDNF), or a combination of GDNF/GDNF receptor α1 (GFRα1) along the corpus callosum. To generate the guidance pathway, adenovirus encoding these transcripts was injected at four positions along the corpus callosum. In all groups, GDNF adenovirus was also injected on the right side 2.5 mm from the midline at the desired transplant site. Four days later, a piece of VM tissue from embryonic day 14 rats was injected at the transplant site. All rats also received daily subcutaneous injections of N-acetyl-L-cysteinamide (NACA; 100 μg per rat) as well as chondroitinase ABC at transplant site (10 U/ml, 2 μl). Two weeks after transplantation, the rats were perfused and the brains dissected out. Coronal sections were cut and immunostained with antibody to tyrosine hydroxylase (TH) to identify and count dopaminergic fibers in the corpus callosum. In GFP-expressing pathways, TH + fibers grew out of the transplants for a short distance in the corpus callosum. Very few TH + fibers grew across the midline. However, pathways expressing GDNF supported more TH + fiber growth across the midline into the contralateral hemisphere. Significantly greater numbers of TH + fibers grew across the midline in animals expressing a combination of GDNF and GFRα1 in the corpus callosum. These data suggest that expression of GDNF or a combination of GDNF and GFRα1 can support the long-distance dopaminergic fiber growth from a VM transplant, with the combination having a superior effect.
AB - To identify guidance molecules to promote long-distance growth of dopaminergic axons from transplanted embryonic ventral mesencephalon (VM) tissue, three pathways were created by expressing green fluorescent protein (GFP), glial cell line-derived neurotrophic factor (GDNF), or a combination of GDNF/GDNF receptor α1 (GFRα1) along the corpus callosum. To generate the guidance pathway, adenovirus encoding these transcripts was injected at four positions along the corpus callosum. In all groups, GDNF adenovirus was also injected on the right side 2.5 mm from the midline at the desired transplant site. Four days later, a piece of VM tissue from embryonic day 14 rats was injected at the transplant site. All rats also received daily subcutaneous injections of N-acetyl-L-cysteinamide (NACA; 100 μg per rat) as well as chondroitinase ABC at transplant site (10 U/ml, 2 μl). Two weeks after transplantation, the rats were perfused and the brains dissected out. Coronal sections were cut and immunostained with antibody to tyrosine hydroxylase (TH) to identify and count dopaminergic fibers in the corpus callosum. In GFP-expressing pathways, TH + fibers grew out of the transplants for a short distance in the corpus callosum. Very few TH + fibers grew across the midline. However, pathways expressing GDNF supported more TH + fiber growth across the midline into the contralateral hemisphere. Significantly greater numbers of TH + fibers grew across the midline in animals expressing a combination of GDNF and GFRα1 in the corpus callosum. These data suggest that expression of GDNF or a combination of GDNF and GFRα1 can support the long-distance dopaminergic fiber growth from a VM transplant, with the combination having a superior effect.
KW - Axon growth
KW - Gene therapy
KW - Neurotrophic factors
KW - Transplantation
KW - Ventral mesencephalon (VM)
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U2 - 10.1002/jnr.22575
DO - 10.1002/jnr.22575
M3 - Article
C2 - 21337366
AN - SCOPUS:79952512033
SN - 0360-4012
VL - 89
SP - 619
EP - 627
JO - Journal of Neuroscience Research
JF - Journal of Neuroscience Research
IS - 5
ER -