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The amino-terminal domain of glutamate receptor delta2 triggers presynaptic differentiation.

机译:谷氨酸受体delta2的氨基末端域触发突触前分化。

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摘要

Glutamate receptor (GluR) delta2 selectively expressed in cerebellar Purkinje cells plays key roles in synapse formation, long-term depression and motor learning. We propose that GluRdelta2 regulates synapse formation by making a physical linkage between the active zone and postsynaptic density. To examine the issue, GluRdelta2-transfected 293T cells were cultured with cerebellar neurons. We found numerous punctate signals for presynaptic markers on the surface of 293T cells expressing GluRdelta2. The presynaptic specializations induced by GluRdelta2 were capable of exo- and endocytosis as indicated by FM1-43 dye labeling. Replacement of the extracellular N-terminal domain (NTD) of GluRdelta2 with that of the AMPA receptor GluRalpha1 abolished the inducing activity. The NTD of GluRdelta2 fused to the immunoglobulin constant region successfully induced the accumulation of presynaptic specializations on the surface of beads bearing the fusion protein. These results suggest that GluRdelta2 triggers presynaptic differentiation by direct interaction with presynaptic components through the NTD.
机译:在小脑浦肯野细胞中选择性表达的谷氨酸受体(GluR)delta2在突触形成,长期抑郁和运动学习中起关键作用。我们建议,GluRdelta2通过在活动区和突触后密度之间建立物理联系来调节突触的形成。为了检查该问题,将GluRdelta2转染的293T细胞与小脑神经元一起培养。我们发现表达GluRdelta2的293T细胞表面上突触前标记的许多点状信号。如FM1-43染料标记所示,GluRdelta2诱导的突触前特化能够胞吐和胞吞作用。用AMPA受体GluRalpha1取代GluRdelta2的细胞外N末端结构域(NTD)消除了诱导活性。融合到免疫球蛋白恒定区的GluRdelta2 NTD成功诱导了突触前特化在带有融合蛋白的珠子表面的积累。这些结果表明,GluRdelta2通过NTD与突触前成分直接相互作用,从而触发突触前分化。

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