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睁眼可差异调节发育中视皮层的抑制性突触传递。

Eye opening differentially modulates inhibitory synaptic transmission in the developing visual cortex.

机构信息

Jing'an District Center Hospital of Shanghai, Institutes of Brain Science, State Key Laboratory of Medical Neurobiology and Collaborative Innovation Center for Brain Science, Fudan University, Shanghai, China.

出版信息

Elife. 2017 Dec 11;6:e32337. doi: 10.7554/eLife.32337.

Abstract

Eye opening, a natural and timed event during animal development, influences cortical circuit assembly and maturation; yet, little is known about its precise effect on inhibitory synaptic connections. Here, we show that coinciding with eye opening, the strength of unitary inhibitory postsynaptic currents (uIPSCs) from somatostatin-expressing interneurons (Sst-INs) to nearby excitatory neurons, but not interneurons, sharply decreases in layer 2/3 of the mouse visual cortex. In contrast, the strength of uIPSCs from fast-spiking interneurons (FS-INs) to excitatory neurons significantly increases during eye opening. More importantly, these developmental changes can be prevented by dark rearing or binocular lid suture, and reproduced by the artificial opening of sutured lids. Mechanistically, this differential maturation of synaptic transmission is accompanied by a significant change in the postsynaptic quantal size. Together, our study reveals a differential regulation in GABAergic circuits in the cortex driven by eye opening may be crucial for cortical maturation and function.

摘要

眼睛睁开是动物发育过程中的一个自然且定时发生的事件,它会影响皮质回路的组装和成熟;然而,人们对其对抑制性突触连接的确切影响知之甚少。在这里,我们发现与眼睛睁开同时发生的是,来自表达生长抑素的中间神经元(Sst-INs)到附近兴奋性神经元的单位抑制性突触后电流(uIPSCs)的强度,而不是中间神经元的强度,在小鼠视觉皮层的 2/3 层急剧下降。相比之下,来自快速放电中间神经元(FS-INs)到兴奋性神经元的 uIPSCs 的强度在眼睛睁开时显著增加。更重要的是,这些发育变化可以通过暗养或双眼睑缝合来预防,并通过缝合眼睑的人工打开来重现。从机制上讲,这种突触传递的差异成熟伴随着突触后量子大小的显著变化。总之,我们的研究揭示了由眼睛睁开驱动的皮层 GABA 能回路的差异调节可能对皮质成熟和功能至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/155a/5746341/096c952a6df5/elife-32337-fig1.jpg

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