Heat-shock protein 70 modulates toxic extracellular α-synuclein oligomers and rescues trans-synaptic toxicity

被引:249
作者
Danzer, Karin M. [1 ]
Ruf, Wolfgang P. [1 ]
Putcha, Preeti [1 ]
Joyner, Daniel [1 ]
Hashimoto, Tadafumi [1 ]
Glabe, Charles [2 ]
Hyman, Bradley T. [1 ]
McLean, Pamela J. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Dept Neurol, MassGen Inst Neurodegenerat Dis,Med Sch, Charlestown, MA 02129 USA
[2] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92717 USA
基金
美国国家卫生研究院;
关键词
Parkinson's disease; aggregation; microfluidic culture system; protein complementation; PARKINSONS-DISEASE; INCLUSION FORMATION; MAMMALIAN-CELLS; LEWY BODIES; PROTEIN; HSP70; STRESS; RELEASE; PATHOLOGY; GLIA;
D O I
10.1096/fj.10-164624
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The paradoxical appearance of aggregated alpha-synuclein (alpha syn) in naive transplanted embryonic stem cells in Parkinson's disease (PD) brains has recently been reported, highlighting the possibility of neuron to neuron transmission of alpha syn in PD. Here, we demonstrate in a cellular model the presence of alpha syn oligomers in the extracellular space, their uptake by neurons, retrograde axonal transport to cell soma, and detrimental effects on neighboring cells. Moreover, we demonstrate that Hsp70 chaperones alpha syn in the extracellular space and reduces extracellular alpha syn oligomer formation and related toxicity. These novel findings provide evidence that extracellular alpha syn oligomers may represent a crucial player in the propagation of pathology in PD, with their modulation by Hsp70 representing a potential new target for therapeutic interventions.-Danzer, K. M., Ruf, W. P., Putcha, P., Joyner, D., Hashimoto, T., Glabe, C., Hyman, B. T., McLean, P. J. Heat-shock protein 70 modulates toxic extracellular alpha-synuclein oligomers and rescues trans-synaptic toxicity. FASEB J. 25, 326-336 (2011). www.fasebj.org
引用
收藏
页码:326 / 336
页数:11
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