Alpha-synuclein supports type 1 interferon signalling in neurons and brain tissue

Author:

Monogue Brendan12,Chen Yixi34,Sparks Hadrian1,Behbehani Ranya3,Chai Andrew3,Rajic Alexander J5,Massey Aaron2,Kleinschmidt-Demasters B K56,Vermeren Matthieu3,Kunath Tilo34ORCID,Beckham J David1257ORCID

Affiliation:

1. Department of Immunology and Microbiology, University of Colorado Anschutz Medical Campus , Aurora, CO 80045 , USA

2. Division of Infectious Diseases, Department of Medicine, University of Colorado Anschutz Medical Campus , Aurora, CO 80045 , USA

3. Centre for Regenerative Medicine and the School of Biological Sciences, University of Edinburgh , Edinburgh EH16 4UU , UK

4. UK Centre for Mammalian Synthetic Biology, University of Edinburgh , Edinburgh EH16 4UU , UK

5. Department of Neurology, University of Colorado Anschutz Medical Campus , Aurora, CO 80045 , USA

6. Departments of Pathology and Neurosurgery, University of Colorado Anschutz Medical Campus , Aurora, CO 80045 , USA

7. Rocky Mountain Regional VA Medical Center , Aurora, CO 80045 , USA

Abstract

Abstract The protein alpha-synuclein is predominantly expressed in neurons and is associated with neurodegenerative diseases like Parkinson’s disease and dementia with Lewy bodies. However, the normal function of alpha-synuclein in neurons is not clearly defined. We have previously shown that mice lacking alpha-synuclein expression exhibit markedly increased viral growth in the brain, increased mortality and increased neuronal cell death, implicating alpha-synuclein in the neuronal innate immune response. To investigate the mechanism of alpha-synuclein-induced immune responses to viral infections in the brain, we challenged alpha-synuclein knockout mice and human alpha-synuclein knockout dopaminergic neurons with RNA virus infection and discovered that alpha-synuclein is required for neuronal expression of interferon-stimulated genes. Furthermore, human alpha-synuclein knockout neurons treated with type 1 interferon failed to induce a broad range of interferon stimulated genes, implying that alpha-synuclein interacts with type 1 interferon signalling. We next found that alpha-synuclein accumulates in the nucleus of interferon-treated human neurons after interferon treatment and we demonstrated that interferon-mediated phosphorylation of STAT2 is dependent on alpha-synuclein expression in human neurons. Next, we found that activated STAT2 co-localizes with alpha-synuclein following type 1 interferon stimulation in neurons. Finally, we found that brain tissue from patients with viral encephalitis expresses increased levels of phospho-serine129 alpha-synuclein in neurons. Taken together, our results show that alpha-synuclein expression supports neuron-specific interferon responses by localizing to the nucleus, supporting STAT2 activation, co-localizing with phosphorylated STAT2 in neurons and supporting expression of interferon-stimulated genes. These data provide a novel mechanism that links interferon activation and alpha-synuclein function in neurons.

Funder

VA Merit Award

NIH

NINDS

NIAID

Mammalian Synthetic Biology

Medical Research Council

Anne Rowling Regenerative Neurology Clinic

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Reference43 articles.

1. The α-synucleinopathies: Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy;Spillantini;Ann N Y Acad Sci,2000

2. The synucleins: A family of proteins involved in synaptic function, plasticity, neurodegeneration and disease;Clayton;Trends Neurosci,1998

3. Red blood cells are the major source of alpha-synuclein in blood;Barbour;Neurodegener Dis,2008

4. Mice lacking α-synuclein display functional deficits in the nigrostriatal dopamine system;Abeliovich;Neuron,2000

5. Double-knockout mice for α- and β-synucleins: Effect on synaptic functions;Chandra;Proc Natl Acad Sci U S A,2004

Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3