Mature enteric neurons have the capacity to reinnervate the intestine with glial cells as their guide.

IF 14.7 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2024-09-25 Epub Date: 2024-07-16 DOI:10.1016/j.neuron.2024.06.018
Rhian Stavely, Ahmed A Rahman, Jessica L Mueller, Abigail R Leavitt, Christopher Y Han, Weikang Pan, Kyla N Kaiser, Leah C Ott, Takahiro Ohkura, Richard A Guyer, Alan J Burns, Abigail N Koppes, Ryo Hotta, Allan M Goldstein
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Abstract

Here, we establish that plasticity exists within the postnatal enteric nervous system by demonstrating the reinnervation potential of post-mitotic enteric neurons (ENs). Employing BAF53b-Cre mice for selective neuronal tracing, the reinnervation capabilities of mature postnatal ENs are shown across multiple model systems. Isolated ENs regenerate neurites in vitro, with neurite complexity and direction influenced by contact with enteric glial cells (EGCs). Nerve fibers from transplanted ENs exclusively interface and travel along EGCs within the muscularis propria. Resident EGCs persist after Cre-dependent ablation of ENs and govern the architecture of the myenteric plexus for reinnervating ENs, as shown by nerve fiber projection tracing. Transplantation and optogenetic experiments in vivo highlight the rapid reinnervation potential of post-mitotic neurons, leading to restored gut muscle contractile activity within 2 weeks. These studies illustrate the structural and functional reinnervation capacity of post-mitotic ENs and the critical role of EGCs in guiding and patterning their trajectories.

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成熟的肠神经元有能力在神经胶质细胞的引导下重新支配肠道。
在这里,我们通过证明有丝分裂后肠神经元(ENs)的神经再支配潜能,证实了可塑性存在于出生后肠神经系统中。利用 BAF53b-Cre 小鼠进行选择性神经元追踪,在多个模型系统中展示了成熟的出生后肠神经元的再神经支配能力。离体EN在体外再生神经元,神经元的复杂性和方向受与肠胶质细胞(EGC)接触的影响。移植EN的神经纤维只与固有肌内的EGCs接触并沿着EGCs移动。正如神经纤维投射追踪所显示的那样,Cre 依赖性消融 ENs 后,驻留的 EGCs 仍然存在,并支配着重新神经支配 ENs 的肠系膜神经丛的结构。体内移植和光遗传实验凸显了有丝分裂后神经元的快速神经再支配潜能,可在两周内恢复肠道肌肉的收缩活动。这些研究说明了有丝分裂后神经元的结构和功能再支配能力,以及EGCs在引导和规划其轨迹方面的关键作用。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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