Directing Dopaminergic Fiber Growth Along a Preformed Molecular Pathway From Embryonic Ventral Mesencephalon Transplants in the Rat Brain

被引:9
作者
Jin, Y. [1 ,2 ]
Zhang, C. [1 ,2 ]
Ziemba, K. S. [1 ,2 ]
Goldstein, G. A. [3 ]
Sullivan, P. G. [2 ,4 ]
Smith, G. M. [1 ,2 ]
机构
[1] Univ Kentucky, Dept Physiol, Lexington, KY 40536 USA
[2] Univ Kentucky, SCoBIRC, Lexington, KY 40536 USA
[3] David Pharmaceut, New York, NY USA
[4] Univ Kentucky, Dept Anat & Neurobiol, Lexington, KY 40536 USA
关键词
axon growth; ventral mesencephalon (VM); transplantation; neurotrophic factors; gene therapy; SPINAL-CORD-INJURY; NEUROTROPHIC FACTOR; AXONAL REGENERATION; ADULT-RAT; PARKINSONS-DISEASE; N-ACETYLCYSTEINE; NEURITE OUTGROWTH; GRAFT-SURVIVAL; NEURONS; RECOVERY;
D O I
10.1002/jnr.22575
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 alpha 1 (GFR alpha 1) 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 mu g per rat) as well as chondroitinase ABC at transplant site (10 U/ml, 2 mu l). 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 GFR alpha 1 in the corpus callosum. These data suggest that expression of GDNF or a combination of GDNF and GFR alpha 1 can support the long-distance dopaminergic fiber growth from a VM transplant, with the combination having a superior effect. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:619 / 627
页数:9
相关论文
共 39 条
[1]   Glial cell line-derived neurotrophic factor improves intrastriatal graft survival of stored dopaminergic cells [J].
Apostolides, C ;
Sanford, E ;
Hong, M ;
Mendez, I .
NEUROSCIENCE, 1998, 83 (02) :363-372
[2]  
BJORKLUND A, 1980, CELL TISSUE RES, V212, P39
[3]   Chondroitinase ABC promotes functional recovery after spinal cord injury [J].
Bradbury, EJ ;
Moon, LDF ;
Popat, RJ ;
King, VR ;
Bennett, GS ;
Patel, PN ;
Fawcett, JW ;
McMahon, SB .
NATURE, 2002, 416 (6881) :636-640
[4]   Evaluation of cellular organization and axonal regeneration through linear PLA foam implants in acute and chronic spinal cord injury [J].
Cai, Jie ;
Ziemba, Kristine S. ;
Smith, George M. ;
Jin, Ying .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2007, 83A (02) :512-520
[5]   Neuroprotective effect of N-acetylcysteine and hypothermia on the spinal cord ischemia-reperfusion injury [J].
Cakir, O ;
Erdem, K ;
Oruc, A ;
Kilinc, N ;
Eren, N .
CARDIOVASCULAR SURGERY, 2003, 11 (05) :375-379
[6]   Inhibitory effect on cerebral inflammatory response following traumatic brain injury in rats: A potential neuroprotective mechanism of N-acetylcysteine [J].
Chen, Gang ;
Shi, Jixin ;
Hu, Zhigang ;
Hang, Chunhua .
MEDIATORS OF INFLAMMATION, 2008, 2008
[7]   AXONAL ELONGATION INTO PERIPHERAL NERVOUS-SYSTEM BRIDGES AFTER CENTRAL NERVOUS-SYSTEM INJURY IN ADULT-RATS [J].
DAVID, S ;
AGUAYO, AJ .
SCIENCE, 1981, 214 (4523) :931-933
[8]  
Diener PS, 1998, J NEUROSCI, V18, P779
[9]  
DOU CL, 1994, J NEUROSCI, V14, P7616
[10]  
Enomoto Hideki, 2005, Anatomical Science International, V80, P42