Erythrocytic α‐Synuclein and the Gut Microbiome: Kindling of the Gut‐Brain Axis in Parkinson's Disease

Author:

Yang Ying123ORCID,Stewart Tessandra4,Zhang Can1,Wang Pan156,Xu Zhi1,Jin Jinghua1,Huang Yang3,Liu Zongran3,Lan Guoyu3,Liang Xingguang7,Sheng Lifu4,Shi Min4,Cai Zhijian8,Zhang Jing1256ORCID

Affiliation:

1. Department of Pathology The First Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China

2. Nanhu Brain‐computer Interface Institute Hangzhou Zhejiang China

3. Department of Pathology Peking University Health Science Center Beijing China

4. Department of Laboratory Medicine and Pathology University of Washington School of Medicine Seattle Washington USA

5. Lingang Laboratory Shanghai China

6. National Human Brain Bank for Health and Disease Zhejiang University Hangzhou China

7. Central Laboratory The First Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China

8. School of Basic Medicine Zhejiang University Hangzhou China

Abstract

AbstractBackgroundProgressive spreading of α‐synuclein via gut‐brain axis has been hypothesized in the pathogenesis of Parkinson's disease (PD). However, the source of seeding‐capable α‐synuclein in the gastrointestinal tract (GIT) has not been fully investigated. Additionally, the mechanism by which the GIT microbiome contributes to PD pathogenesis remains to be characterized.ObjectivesWe aimed to investigate whether blood‐derived α‐synuclein might contribute to PD pathology via a gut‐driven pathway and involve GIT microbiota.MethodsThe GIT expression of α‐synuclein and the transmission of extracellular vesicles (EVs) derived from erythrocytes/red blood cells (RBCs), with their cargo α‐synuclein, to the GIT were explored with various methods, including radioactive labeling of RBC‐EVs and direct analysis of the transfer of α‐synuclein protein. The potential role of microbiota on the EVs transmission was further investigated by administering butyrate, the short‐chain fatty acids produced by gut microbiota and studying mice with different α‐synuclein genotypes.ResultsThis study demonstrated that RBC‐EVs can effectively transport α‐synuclein to the GIT in a region‐dependent manner, along with variations closely associated with regional differences in the expression of gut‐vascular barrier markers. The investigation further revealed that the infiltration of α‐synuclein into the GIT was influenced significantly by butyrate and α‐synuclein genotypes, which may also affect the GIT microbiome directly.ConclusionBy demonstrating the transportation of α‐synuclein through RBC‐EVs to the GIT, and its potential association with gut‐vascular barrier markers and gut microbiome, this work highlights a potential mechanism by which RBC α‐synuclein may impact PD initiation and/or progression. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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