Gu Zirong, Serradj Najet, Ueno Masaki, Liang Mishi, Li Jie, Baccei Mark L, Martin John H, Yoshida Yutaka
Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Department of Physiology, Pharmacology and Neuroscience, City University of New York School of Medicine, New York, NY 10031, USA.
Neuron. 2017 May 3;94(3):626-641.e4. doi: 10.1016/j.neuron.2017.04.019.
Early postnatal mammals, including human babies, can perform only basic motor tasks. The acquisition of skilled behaviors occurs later, requiring anatomical changes in neural circuitry to support the development of coordinated activation or suppression of functionally related muscle groups. How this circuit reorganization occurs during postnatal development remains poorly understood. Here we explore the connectivity between corticospinal (CS) neurons in the motor cortex and muscles in mice. Using trans-synaptic viral and electrophysiological assays, we identify the early postnatal reorganization of CS circuitry for antagonistic muscle pairs. We further show that this synaptic rearrangement requires the activity-dependent, non-apoptotic Bax/Bak-caspase signaling cascade. Adult Bax/Bak mutant mice exhibit aberrant co-activation of antagonistic muscle pairs and skilled grasping deficits but normal reaching and retrieval behaviors. Our findings reveal key cellular and molecular mechanisms driving postnatal motor circuit reorganization and the resulting impacts on muscle activation patterns and the execution of skilled movements.
包括人类婴儿在内的出生后早期哺乳动物只能执行基本的运动任务。熟练行为的习得发生在后期,需要神经回路的解剖学变化来支持功能相关肌肉群协调激活或抑制的发展。这种回路重组在出生后发育过程中是如何发生的,目前仍知之甚少。在这里,我们探索了小鼠运动皮层中皮质脊髓(CS)神经元与肌肉之间的连接性。使用跨突触病毒和电生理检测方法,我们确定了出生后早期CS回路中拮抗肌对的重组。我们进一步表明,这种突触重排需要依赖活动的、非凋亡的Bax/Bak-半胱天冬酶信号级联反应。成年Bax/Bak突变小鼠表现出拮抗肌对的异常共同激活和熟练抓握缺陷,但伸手和取回行为正常。我们的研究结果揭示了驱动出生后运动回路重组的关键细胞和分子机制,以及对肌肉激活模式和熟练运动执行的影响。