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Prothrombin kringle-2 induces death of mesencephalic dopaminergic neurons in vivo and in vitro via microglial activation.

Kim, SR; Chung, ES; Bok, E; Baik, HH; Chung, YC; Won, SY; Joe, E; Kim, TH; Kim, SS; Jin, MY; Choi, SH; Jin, BK
Journal of neuroscience research, 88(7):1537-1548, 2010
Journal Title
Journal of neuroscience research
We have shown that prothrombin kringle-2 (pKr-2), a domain of human prothrombin distinct from thrombin could activate cultured rat brain microglia in vitro. However, little is known whether pKr-2-induced microglial activation could cause neurotoxicity on dopaminergic (DA) neurons in vivo. To address this question, pKr-2 was injected into the rat substantia nigra (SN). Tyrosine hydroxylase (TH) immunohistochemistry experiments demonstrate significant loss of DA neurons seven days after injection of pKr-2. In parallel, pKr-2-activated microglia were detected in the SN with OX-42 and OX-6 immunohistochemistry. Reverse transcription PCR and double-label immunohistochemistry revealed that activated microglia in vivo exhibit early and transient expression of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2) and several proinflammatory cytokines. The pKr-2-induced loss of SN DA neurons was partially inhibited by the NOS inhibitor N(G)-nitro-L-arginine methyl ester hydrochloride, and the COX-2 inhibitor DuP-697. Extracellular signal-regulated kinase 1/2, c-Jun N-terminal kinase and p38 mitogen-activated protein kinase were activated in the SN as early as 1 hr after pKr-2 injection, and localized within microglia. Inhibition of these kinases led to attenuation of mRNA expression of iNOS, COX-2 and several proinflammatory cytokines, and rescue of DA neurons in the SN. Intriguingly, following treatment with pKr-2 in vitro, neurotoxicity was detected exclusively in co-cultures of mesencephalic neurons and microglia, but not microglia-free neuron-enriched mesencephalic cultures, indicating that microglia are required for pKr-2 neurotoxicity. Our results strongly suggest that microglia activated by endogenous compound(s), such as pKr-2, are implicated in the DA neuronal cell death in the SN.
MeSH terms
AnimalsAntigens, CD11b/analysisAntigens, CD11b/metabolismCells, CulturedCoculture TechniquesCyclooxygenase 2/drug effectsCyclooxygenase 2/geneticsCyclooxygenase 2/metabolismCyclooxygenase 2 Inhibitors/pharmacologyDopamine/metabolism*FemaleGliosis/chemically inducedGliosis/metabolism*Gliosis/physiopathologyInflammation Mediators/metabolismKringles/physiologyMAP Kinase Signaling System/drug effectsMAP Kinase Signaling System/physiologyMicroglia/drug effectsMicroglia/metabolism*Neurons/drug effectsNeurons/metabolism*Nitric Oxide Synthase/antagonists & inhibitorsNitric Oxide Synthase/metabolismNitric Oxide Synthase Type II/antagonists & inhibitorsNitric Oxide Synthase Type II/geneticsNitric Oxide Synthase Type II/metabolismParkinson Disease/metabolismParkinson Disease/physiopathologyProthrombin/chemistryProthrombin/metabolism*Prothrombin/toxicityRNA, Messenger/drug effectsRNA, Messenger/metabolismRatsRats, Sprague-DawleySubstantia Nigra/drug effectsSubstantia Nigra/metabolism*Substantia Nigra/physiopathology
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Journal Papers > School of Medicine / Graduate School of Medicine > Pharmacology
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