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Fig. 3 | Acta Neuropathologica Communications

Fig. 3

From: In Parkinson's patient-derived dopamine neurons, the triplication of α-synuclein locus induces distinctive firing pattern by impeding D2 receptor autoinhibition

Fig. 3

Both AST-derived dopamine neurons and mouse dopamine neurons overexpressing α-synuclein exhibit bursting firing pattern. The experiments and analyses were performed in parallel and via a blinded experimental design. a1 Representative trace of a spontaneously active NAS-derived dopamine neurons shows a mixture of single spikes and small burst activity with an underlying “pacemaker-like” periodicity. a2 Representative trace of a spontaneously active AST-derived dopamine neuron shows a unique high up-state (depolarized plateau) and high frequency of spontaneous activity with a pause between subsequent broadbrimmed bursts. a3 Time courses of instantaneous firing frequency, action potential half-width and amplitude obtained from (a1) and (a2). b1 Representative trace of a spontaneously active wild type mouse dopamine neuron obtained from midbrain primary neuronal culture. b2 Representative trace of a spontaneously active mouse dopamine neuron overexpressing α-synuclein. b3 Time courses of instantaneous firing frequency, action potential half-width and amplitude obtained from b1 and b2. c Phase-plane plot of action potentials generated from (a1) and (a2). Unlike AST-derived dopamine neurons, the action potentials in NAS-derived dopamine neurons show a smooth and slower onset at initiation site. d Phase-plane plot of action potentials generated from b1 and b2. e Interspike histogram (in ms) from top to bottom: NAS-, AST-derived neurons, WT mouse dopamine neurons, and mouse dopamine neurons overexpressing α-synuclein. n corresponds to the total number of spikes for each histogram

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