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RNA 结合蛋白 NANOS1 控制海马突触发生。

The RNA-binding protein NANOS1 controls hippocampal synaptogenesis.

机构信息

Fundación Instituto Leloir (FIL), Buenos Aires, Argentina.

Instituto de Investigaciones Bioquímicas de Buenos Aires (IIBBA) - Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET), Buenos Aires, Argentina.

出版信息

PLoS One. 2023 Apr 14;18(4):e0284589. doi: 10.1371/journal.pone.0284589. eCollection 2023.

Abstract

Proteins from the NANOS family are conserved translational repressors with a well-known role in gonad development in both vertebrates and invertebrates. In addition, Drosophila Nanos controls neuron maturation and function, and rodent Nanos1 affects cortical neuron differentiation. Here we show that rat Nanos1 is expressed in hippocampal neurons and that the siRNA-mediated knockdown of Nanos1 impairs synaptogenesis. We found that both dendritic spine size and number were affected by Nanos1 KD. Dendritic spines were smaller and more numerous. Moreover, whereas in control neurons most dendritic PSD95 clusters contact pre-synaptic structures, a larger proportion of PSD95 clusters lacked a synapsin counterpart upon Nanos1 loss-of-function. Finally, Nanos1 KD impaired the induction of ARC typically triggered by neuron depolarization. These results expand our knowledge on the role of NANOS1 in CNS development and suggest that RNA regulation by NANOS1 governs hippocampal synaptogenesis.

摘要

NANOS 家族的蛋白质是保守的翻译抑制剂,在脊椎动物和无脊椎动物的性腺发育中具有重要作用。此外,果蝇 Nanos 控制神经元的成熟和功能,而啮齿动物 Nanos1 影响皮质神经元的分化。在这里,我们发现大鼠 Nanos1 在海马神经元中表达,并且 siRNA 介导的 Nanos1 敲低会损害突触发生。我们发现树突棘的大小和数量都受到 Nanos1 KD 的影响。树突棘更小,数量更多。此外,在对照神经元中,大多数树突 PSD95 簇与突触前结构接触,而在 Nanos1 功能丧失时,更大比例的 PSD95 簇缺乏突触小泡对应物。最后,Nanos1 KD 会损害通常由神经元去极化引发的 ARC 的诱导。这些结果扩展了我们对 NANOS1 在中枢神经系统发育中的作用的认识,并表明 NANOS1 通过 RNA 调控控制海马突触发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e37e/10104283/847c0a493bf8/pone.0284589.g001.jpg

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