4.7 Article

alpha-Synuclein-containing erythrocytic extracellular vesicles: essential contributors to hyperactivation of monocytes in Parkinson's disease

期刊

JOURNAL OF NEUROINFLAMMATION
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12974-022-02413-1

关键词

Extracellular vesicles; RBC; alpha-Synuclein; Parkinson's disease; Monocytes; LRRK2

资金

  1. National Key Research and Development Program of China-2016YFC1306500, China Postdoctoral Science [Foundation-2020M670063, 2020T130030, 81571226, 82020108012, 81671187]

向作者/读者索取更多资源

This study found that alpha-synuclein derived from red blood cells mediates the sensitization of peripheral monocytes in patients with Parkinson's disease. This process leads to increased inflammatory activity in monocytes.
Background: Immune system dysfunction, including higher levels of peripheral monocytes and inflammatory cytokines, is an important feature of Parkinson's disease (PD) pathogenesis, although the mechanism underlying the process remains to be investigated. In the central nervous system, it is well-known that alpha-synuclein (alpha-syn), a key protein involved in PD, activates microglia potently, and it is also reported that alpha-syn exists in the peripheral system, especially in erythrocytes or red blood cells (RBC) at exceedingly high concentration. The current study focused on the possibility that RBC-derived alpha-syn mediates the sensitization of peripheral monocytes in PD patients. Methods: The hyperactivation of monocytes was assessed quantitatively by measuring mRNA levels of typical inflammatory cytokines (including IL-1 beta, IL-6 and TNF-alpha) and protein levels of secreted inflammatory cytokines (including pro-inflammatory cytokines: IL-1 beta, IL-6, TNF-alpha, IL-8, IFN-gamma, IL-2, and IL-12p70 and anti-inflammatory cytokines: IL-4, IL-10, and IL-13). Western blot, nanoparticle tracking analysis and electron microscopy were used to characterize RBC-derived extracellular vesicles (RBC-EVs). Inhibitors of endocytosis and leucine-rich repeat kinase 2 (LRRK2), another key protein involved in PD, were used to investigate how these two factors mediated the process of monocyte sensitization by RBC-EVs. Results: Increased inflammatory sensitization of monocytes was observed in PD patients and PD model mice. We found that alpha-syn-containing RBC-EVs isolated from PD model mice or free form oligomeric alpha-syn induced the inflammatory sensitization of THP-1 cells, and demonstrated that endocytosis was a requirement for this pathophysiological pathway. Furthermore, the hyperactivation of THP-1 cells induced by RBC-EVs was associated with increased LRRK2 production and kinase activity. The phenomenon of inflammatory sensitization of human monocytes and increased LRRK2 were also observed by the treatment of RBC-EVs isolated from PD patients. Conclusions: Our data provided new insight into how hyperactivation of monocytes occurs in PD patients, and identified the central role played by alpha-syn-containing RBC-EVs in this process.

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