Semi-quantitative analysis of alpha-synuclein in subcellular pools of rat brain neurons: An immunogold electron microscopic study using a C-terminal specific monoclonal antibody
机构:[a]Beijing Institute for Neuroscience, Capital Medical University (CMU), Beijing Center of Neural Regeneration and Repairing, Beijing 100069, China[b]Department of Neurobiology, Beijing Institute of Geriatrics, Xuanwu Hospital of CMU, Beijing 100053, China老年医学科首都医科大学宣武医院[c]Key Laboratory for Neurodegenerative Diseases of Ministry of Education, Beijing 100069, China[d]Division of Psychobiology, Tokyo Institute of Psychiatry, Tokyo 156-8585, Japan
alpha-Synuclein (alpha-Syn) is a brain-enriched protein of 140 amino acids. Despite of strong evidence showing the implication of the protein in the pathogenesis of several neuro degenerative diseases, its physiological function remains poorly understood. To study the physiological function of alpha-Syn, a depiction of its precise subcellular localization is necessary. Although alpha-Syn expression in the brain has been extensively investigated using several different antibodies, its precise subcellular localization in neurons remains elusive. In this study, immunogold electron microscopy with a newly produced 3D5 monoclonal antibody recognizing the C-terminal 115-121 amino acids of alpha-Syn was used to examine its subcellular localization in rat brain neurons. in addition, the relative amount of the protein in different subcellular pools of the neurons in several brain regions was evaluated and compared. The results showed that alpha-Syn-positive gold particles were unevenly distributed in axons, presynaptic terminals, cytoplasm and nucleus in the neuron, with the density of gold particles being greater in presynaptic terminals and nucleus than in other subcellular pools. In the cytoplasmic region, relatively dense gold particles were seen in some mitochondria. in the same subcellular pools, the density of gold particles was varied among the neurons from different brain regions. Although the cortical neurons showed much higher density of gold particles in the presynaptic terminals and nuclei than in striatal, hippocampal and substantia nigral neurons, the density of gold particles in their mitochondria was much lower compared with the mitochondria of striatal, hippocampal and substantia nigral neurons. The relative high level of mitochondrial alpha-Syn in hippocampus, striatum and substantia nigral neurons may have special pathophysiological significance, which deserves further investigation. (C) 2008 Published by Elsevier B.V.
基金:
The National Basic Research Program of China (2006CB500706), National Natural Science Foundation of China (30670655, 30570646, 30430280),
National Ministry of Education (20060025004), Beijing Municipal Education Commission(KM200610025002), and National High-Tech R and D Program of China (2006AA02A408).
第一作者机构:[a]Beijing Institute for Neuroscience, Capital Medical University (CMU), Beijing Center of Neural Regeneration and Repairing, Beijing 100069, China[c]Key Laboratory for Neurodegenerative Diseases of Ministry of Education, Beijing 100069, China
通讯作者:
通讯机构:[a]Beijing Institute for Neuroscience, Capital Medical University (CMU), Beijing Center of Neural Regeneration and Repairing, Beijing 100069, China
推荐引用方式(GB/T 7714):
Ling Zhang,Chunyan Zhang,Yuangang Zhu,et al.Semi-quantitative analysis of alpha-synuclein in subcellular pools of rat brain neurons: An immunogold electron microscopic study using a C-terminal specific monoclonal antibody[J].BRAIN RESEARCH.2008,1244:40-52.doi:10.1016/j.brainres.2008.08.067.
APA:
Ling Zhang,Chunyan Zhang,Yuangang Zhu,Qing Cai,Piu Chan...&Hui Yang.(2008).Semi-quantitative analysis of alpha-synuclein in subcellular pools of rat brain neurons: An immunogold electron microscopic study using a C-terminal specific monoclonal antibody.BRAIN RESEARCH,1244,
MLA:
Ling Zhang,et al."Semi-quantitative analysis of alpha-synuclein in subcellular pools of rat brain neurons: An immunogold electron microscopic study using a C-terminal specific monoclonal antibody".BRAIN RESEARCH 1244.(2008):40-52