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利用新型GRAB传感器检测培养的皮质神经元中内源性神经肽Y的释放。

Detection of endogenous NPY release determined by novel GRAB sensor in cultured cortical neurons.

作者信息

Christensen Emma Kragelund, Konomi-Pilkati Ainoa, Rombach Joscha, Comaposada-Baro Raquel, Wang Huan, Li Yulong, Sørensen Andreas Toft

机构信息

Molecular Neuropharmacology and Genetics Laboratory, Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

State Key Laboratory of Membrane Biology, Peking University School of Life Sciences, Beijing, China.

出版信息

Front Cell Neurosci. 2023 Jul 20;17:1221147. doi: 10.3389/fncel.2023.1221147. eCollection 2023.

Abstract

Neuropeptide Y (NPY) is an abundantly expressed peptide in the nervous system. Its widespread distribution along with its receptors, both centrally and peripherally, indicates its broad functions in numerous biological processes. However, the low endogenous concentration and diffuse distribution of NPY make it challenging to study its actions and dynamics directly and comprehensively. Studies on the role of NPY have primarily been limited to exogenous application, transgene expression, or knock-out in biological systems, which are often combined with pharmacological probes to delineate the involvement of specific NPY receptors. Therefore, to better understand the function of NPY in time and space, direct visualization of the real-time dynamics of endogenous NPY is a valuable and desired tool. Using the first-generation and newly developed intensiometric green fluorescent G-protein-coupled NPY sensor (GRAB NPY1.0), we, for the first time, demonstrate and characterize the direct detection of endogenously released NPY in cultured cortical neurons. A dose-dependent fluorescent signal was observed upon exogenous NPY application in nearly all recorded neurons. Pharmacologically evoked neuronal activity induced a significant increase in fluorescent signal in 32% of neurons, reflecting the release of NPY, despite only 3% of all neurons containing NPY. The remaining pool of neurons expressing the sensor were either non-responsive or displayed a notable decline in the fluorescent signal. Such decline in fluorescent signal was not rescued in cortical cultures transduced with an NPY overexpression vector, where 88% of the neurons were NPY-positive. Overexpression of NPY did, however, result in sensor signals that were more readily distinguishable. This may suggest that biological factors, such as subtle changes in intracellular pH, could interfere with the fluorescent signal, and thereby underestimate the release of endogenous NPY when using this new sensor in its present configuration. However, the development of next-generation NPY GRAB sensor technology is expected soon, and will eventually enable much-wanted studies on endogenous NPY release dynamics in both cultured and intact biological systems.

摘要

神经肽Y(NPY)是神经系统中大量表达的一种肽。它及其受体在中枢和外周广泛分布,表明其在众多生物过程中具有广泛功能。然而,NPY的内源性浓度较低且分布弥散,这使得直接全面地研究其作用和动态具有挑战性。对NPY作用的研究主要局限于生物系统中的外源性应用、转基因表达或基因敲除,这些通常与药理学探针相结合,以阐明特定NPY受体的参与情况。因此,为了更好地在时间和空间上理解NPY的功能,对内源性NPY实时动态的直接可视化是一种有价值且令人期待的工具。使用第一代和新开发的强度型绿色荧光G蛋白偶联NPY传感器(GRAB NPY1.0),我们首次展示并表征了在培养的皮质神经元中直接检测内源性释放的NPY。在几乎所有记录的神经元中外源性应用NPY时观察到剂量依赖性荧光信号。药理学诱发的神经元活动在32%的神经元中诱导荧光信号显著增加,反映了NPY的释放,尽管所有神经元中只有3%含有NPY。其余表达该传感器的神经元池要么无反应,要么荧光信号显著下降。在用NPY过表达载体转导的皮质培养物中,荧光信号的这种下降并未得到挽救,其中88%的神经元是NPY阳性的。然而,NPY的过表达确实导致传感器信号更容易区分。这可能表明生物因素,如细胞内pH的细微变化,可能会干扰荧光信号,从而在使用当前配置的这种新传感器时低估内源性NPY的释放。然而,预计下一代NPY GRAB传感器技术很快就会出现,最终将能够对培养的和完整的生物系统中的内源性NPY释放动态进行备受期待的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1248/10399118/7ce577a42ad9/fncel-17-1221147-g001.jpg

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