Is Axonal Degeneration a Key Early Event in Parkinson's Disease?

被引:46
|
作者
Kurowska, Zuzanna [1 ,2 ]
Kordower, Jeffrey H. [3 ,4 ]
Stoessl, A. Jon [5 ,6 ]
Burke, Robert E. [7 ,8 ]
Brundin, Patrik [4 ]
Yue, Zhenyu [9 ,10 ]
Brady, Scott T. [11 ,12 ]
Milbrandt, Jeffrey [13 ,14 ]
Trappa, Bruce D. [1 ,2 ]
Sherer, Todd B. [15 ]
Medicetty, Satish [2 ]
机构
[1] Cleveland Clin, Dept Neurosci, Lerner Res Inst, 9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Renovo Neural Inc, Cleveland, OH USA
[3] Rush Univ, Med Ctr, Res Ctr Brain Repair, Chicago, IL 60612 USA
[4] Van Andel Res Inst, Ctr Neurodegenerat Sci, Grand Rapids, MI USA
[5] Univ British Columbia & Vancouver Coastal Hlth, Pacific Parkinsons Res Ctr, Div Neurol, Vancouver, BC, Canada
[6] Univ British Columbia & Vancouver Coastal Hlth, Djavad Mowafaghian Ctr Brain Hlth, Vancouver, BC, Canada
[7] Columbia Univ, Med Ctr, Dept Neurol & Pathol, New York, NY USA
[8] Columbia Univ, Med Ctr, Dept Cell Biol, New York, NY USA
[9] Icahn Sch Med Mt Sinai, Dept Neurol, Friedman Brain Inst, New York, NY 10029 USA
[10] Icahn Sch Med Mt Sinai, Dept Neurosci, Friedman Brain Inst, New York, NY 10029 USA
[11] Univ Illinois, Dept Anat & Cell Biol, Chicago, IL USA
[12] Marine Biol Lab, Woods Hole, MA 02543 USA
[13] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[14] Washington Univ, Sch Med, Hope Ctr Neurol Disorders, St Louis, MO USA
[15] Michael J Fox Fdn Parkinsons Res, New York, NY USA
关键词
Parkinson disease; axons; animal disease models; autophagy; review; dopaminergic neurons; substantia nigra pars compacta; synapses; axonal transport; retrograde degeneration; DOPAMINERGIC-NEURONS; MULTIPLE-SCLEROSIS; ALPHA-SYNUCLEIN; MODEL; DYSFUNCTION; TRANSPORT; MIDBRAIN; DESTRUCTION; PROGRESSION; ENGRAILED1;
D O I
10.3233/JPD-160881
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent research suggests that in Parkinson's disease the long, thin and unmyelinated axons of dopaminergic neurons degenerate early in the disease process. We organized a workshop entitled 'Axonal Pathology in Parkinson's disease', on March 23rd, 2016, in Cleveland, Ohio with the goals of summarizing the state-of-the-art and defining key gaps in knowledge. A group of eight research leaders discussed new developments in clinical pathology, functional imaging, animal models, and mechanisms of degeneration including neuroinflammation, autophagy and axonal transport deficits. While the workshop focused on PD, comparisons were made to other neurological conditions where axonal degeneration is well recognized.
引用
收藏
页码:703 / 707
页数:5
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