α-Synuclein activates stress signaling protein kinases in THP-1 cells and microglia

Abstract 

Here we show that α-synuclein, a major constituent of Lewy bodies, induces inflammation in human microglial and human THP-1 cells. Secretions from such stimulated THP-1 cells contain increased levels of IL-1β and TNF-α. When stimulated by α-synuclein in combination with IFN-γ, secretions from the cells also become toxic towards SH-SY5Y neuroblastoma cells. The A30P, E46K and A53T α-synuclein mutations, which induce Parkinson's disease, are more potent than normal α-synuclein in the induction of such cytotoxicity. To investigate the signaling mechanisms evoked, protein phosphorylation profiling was applied. At least 81 target phospho-sites were identified. Large increases were induced in the three major mitogen-activated protein (MAP) kinase pathways: p38 MAP kinase, extracellular regulated protein-serine kinase (ERK)1/2 and c-Jun-N-terminal kinase (JNK). Upregulation occurred within minutes following exposure to α-synuclein, which is consistent with a receptor-mediated effect. These findings demonstrate that α-synuclein acts as a potent inflammatory stimulator of microglial cells, and that inhibitors of such stimulation might be beneficial in the treatment of Parkinson's disease and other synucleinopathies.

Keywords: Cytokines, c-Jun N-terminal kinase (JNK), Human glial cells, MAPK/ERK kinase (MEK), Neuroinflammation, Neurotoxicity, p38 Mitogen-activated protein (MAP) kinase, Parkinson's disease, Phosphorylation