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通过新皮层投射神经元的直接谱系重编程指导体细胞周围抑制

Instructing Perisomatic Inhibition by Direct Lineage Reprogramming of Neocortical Projection Neurons.

作者信息

Ye Zhanlei, Mostajo-Radji Mohammed A, Brown Juliana R, Rouaux Caroline, Tomassy Giulio Srubek, Hensch Takao K, Arlotta Paola

机构信息

Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA; Center for Brain Science, Harvard University, Cambridge, MA 02138, USA.

Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA.

出版信息

Neuron. 2015 Nov 4;88(3):475-83. doi: 10.1016/j.neuron.2015.10.006.

Abstract

During development of the cerebral cortex, local GABAergic interneurons recognize and pair with excitatory projection neurons to ensure the fine excitatory-inhibitory balance essential for proper circuit function. Whether the class-specific identity of projection neurons has a role in the establishment of afferent inhibitory synapses is debated. Here, we report that direct in vivo lineage reprogramming of layer 2/3 (L2/3) callosal projection neurons (CPNs) into induced corticofugal projection neurons (iCFuPNs) increases inhibitory input onto the converted neurons to levels similar to that of endogenous CFuPNs normally found in layer 5 (L5). iCFuPNs recruit increased numbers of inhibitory perisomatic synapses from parvalbumin (PV)-positive interneurons, with single-cell precision and despite their ectopic location in L2/3. The data show that individual reprogrammed excitatory projection neurons extrinsically modulate afferent input by local PV(+) interneurons, suggesting that projection neuron class-specific identity can actively control the wiring of the cortical microcircuit.

摘要

在大脑皮质发育过程中,局部γ-氨基丁酸能中间神经元识别并与兴奋性投射神经元配对,以确保对正常回路功能至关重要的精细兴奋性-抑制性平衡。投射神经元的类别特异性身份在传入抑制性突触的建立中是否起作用存在争议。在这里,我们报告将第2/3层(L2/3)胼胝体投射神经元(CPN)直接在体内重编程为诱导皮质离心投射神经元(iCFuPN),会增加转换神经元上的抑制性输入,使其水平与通常在第5层(L5)发现的内源性CFuPN相似。iCFuPN从小白蛋白(PV)阳性中间神经元募集数量增加的抑制性胞体周围突触,具有单细胞精度,尽管它们在L2/3中位置异位。数据表明,单个重编程的兴奋性投射神经元通过局部PV(+)中间神经元外在调节传入输入,这表明投射神经元类别特异性身份可以积极控制皮质微回路的布线。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c31/4794746/6b243b22259d/nihms734314f1.jpg

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