Neuronal Dysfunction in iPSC-Derived Medium Spiny Neurons from Chorea-Acanthocytosis Patients Is Reversed by Src Kinase Inhibition and F-Actin Stabilization

作者：Stanslowsky Nancy; Reinhardt Peter; Glass Hannes; Kalmbach Norman; Naujock Maximilian; Hensel Niko; Luebben Verena; Pal Arun; Venneri Xanna; Lupo Francesca; De Franceschi Lucia; Claus Peter; Sterneckert Jared; Storch Alexander; Hermann Andreas; Wegner Florian^*

来源：Journal of Neuroscience, 2016, 36(47): 12027-12043.

DOI：10.1523/JNEUROSCI.0456-16.2016

• actin cytoskeleton
• chorea-acanthocytosis
• human induced pluripotent stem cells
• patch-clamp electrophysiology
• Src kinase
• striatal medium spiny neurons

Chorea-acanthocytosis (ChAc) is a fatal neurological disorder characterized by red blood cell acanthocytes and striatal neurodegeneration. Recently, severe cell membrane disturbances based on depolymerized cortical actin and an elevated Lyn kinase activity in erythrocytes from ChAc patients were identified. How this contributes to the mechanism of neurodegeneration is still unknown. To gain insight into the pathophysiology, we established a ChAc patient-derived induced pluripotent stem cell model and an efficient differentiation protocol providing a large population of human striatal medium spiny neurons (MSNs), the main target of neurodegeneration in ChAc. Patient-derived MSNs displayed enhanced neurite outgrowth and ramification, whereas synaptic density was similar to controls. Electrophysiological analysis revealed a pathologically elevated synaptic activity in ChAc MSNs. Treatment with the F-actin stabilizer phallacidin or the Src kinase inhibitor PP2 resulted in the significant reduction of disinhibited synaptic currents to healthy control levels, suggesting a Src kinase-and actin-dependent mechanism. This was underlined by increased G/F-actin ratios and elevated Lyn kinase activity in patient-derived MSNs. These data indicate that F-actin stabilization and Src kinase inhibition represent potential therapeutic targets in ChAc that may restore neuronal function.

• 出版日期2016-11-23