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半胱氨酸-string 蛋白-α的磷酸化上调了胆碱能波星爆型无长突细胞的频率。

Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves starburst amacrine cells.

机构信息

Institute of Molecular and Cellular Biology, National Taiwan University, Taipei, Taiwan.

Department of Physiology and Pharmacology, College of Medicine, Chang Gung University, Taoyuan, Taiwan.

出版信息

Vis Neurosci. 2022 May 11;39:E003. doi: 10.1017/S0952523822000013.

Abstract

During the first postnatal week in rodents, cholinergic retinal waves initiate in starburst amacrine cells (SACs), propagating to retinal ganglion cells (RGCs) and visual centers, essential for visual circuit refinement. By modulating exocytosis in SACs, dynamic changes in the protein kinase A (PKA) activity can regulate the spatiotemporal patterns of cholinergic waves. Previously, cysteine string protein-α (CSPα) is found to interact with the core exocytotic machinery by PKA-mediated phosphorylation at serine 10 (S10). However, whether PKA-mediated CSPα phosphorylation may regulate cholinergic waves via SACs remains unknown. Here, we examined how CSPα phosphorylation in SACs regulates cholinergic waves. First, we identified that CSPα1 is the major isoform in developing rat SACs and the inner plexiform layer during the first postnatal week. Using SAC-specific expression, we found that the CSPα1-PKA-phosphodeficient mutant (CSP-S10A) decreased wave frequency, but did not alter the wave spatial correlation compared to control, wild-type CSPα1 (CSP-WT), or two PKA-phosphomimetic mutants (CSP-S10D and CSP-S10E). These suggest that CSPα-S10 phosphodeficiency in SACs dampens the frequency of cholinergic waves. Moreover, the level of phospho-PKA substrates was significantly reduced in SACs overexpressing CSP-S10A compared to control or CSP-WT, suggesting that the dampened wave frequency is correlated with the decreased PKA activity. Further, compared to control or CSP-WT, CSP-S10A in SACs reduced the periodicity of wave-associated postsynaptic currents (PSCs) in neighboring RGCs, suggesting that these RGCs received the weakened synaptic inputs from SACs overexpressing CSP-S10A. Finally, CSP-S10A in SACs decreased the PSC amplitude and the slope to peak PSC compared to control or CSP-WT, suggesting that CSPα-S10 phosphodeficiency may dampen the speed of the SAC-RGC transmission. Thus, via PKA-mediated phosphorylation, CSPα in SACs may facilitate the SAC-RGC transmission, contributing to the robust frequency of cholinergic waves.

摘要

在啮齿动物出生后的第一周,星状胶质细胞(SAC)中的胆碱能视网膜波起始,传播到视网膜神经节细胞(RGC)和视觉中枢,这对于视觉回路的细化至关重要。通过调节 SAC 中的胞吐作用,蛋白激酶 A(PKA)活性的动态变化可以调节胆碱能波的时空模式。以前,发现半胱氨酸串蛋白-α(CSPα)通过 PKA 介导的丝氨酸 10(S10)磷酸化与核心胞吐机制相互作用。然而,PKA 介导的 CSPα 磷酸化是否可以通过 SAC 调节胆碱能波尚不清楚。在这里,我们研究了 SAC 中的 CSPα 磷酸化如何调节胆碱能波。首先,我们确定 CSPα1 是发育中的大鼠 SAC 和出生后第一周内内丛状层中的主要同工型。使用 SAC 特异性表达,我们发现 CSPα1-PKA-磷酸缺陷型突变体(CSP-S10A)与对照、野生型 CSPα1(CSP-WT)或两个 PKA-磷酸模拟突变体(CSP-S10D 和 CSP-S10E)相比,降低了波频率,但不改变波空间相关性。这表明 SAC 中的 CSPα-S10 磷酸缺陷减弱了胆碱能波的频率。此外,与对照或 CSP-WT 相比,过表达 CSP-S10A 的 SAC 中的磷酸化 PKA 底物水平显著降低,表明减弱的波频率与 PKA 活性降低相关。此外,与对照或 CSP-WT 相比,SAC 中的 CSP-S10A 减少了相邻 RGC 中与波相关的突触后电流(PSC)的周期性,表明这些 RGC 从过表达 CSP-S10A 的 SAC 接收了减弱的突触输入。最后,与对照或 CSP-WT 相比,SAC 中的 CSP-S10A 降低了 PSC 幅度和峰值 PSC 的斜率,表明 CSPα-S10 磷酸缺陷可能会降低 SAC-RGC 传递的速度。因此,通过 PKA 介导的磷酸化,SAC 中的 CSPα 可能促进 SAC-RGC 传递,有助于胆碱能波的强大频率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee27/9107963/caa6833993fd/S0952523822000013_fig1.jpg

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