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Altered presynaptic function and number of mitochondria in the medial prefrontal cortex of adult Cyfip2 heterozygous mice

机译:在成人Cyfip2杂合小鼠的内侧前额叶皮质中改变了突触前功能和线粒体数量

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摘要

Variants of the cytoplasmic FMR1-interacting protein (CYFIP) gene family, CYFIP1 and CYFIP2, are associated with numerous neurodevelopmental and neuropsychiatric disorders. According to several studies, CYFIP1 regulates the development and function of both pre- and post-synapses in neurons. Furthermore, various studies have evaluated CYFIP2 functions in the postsynaptic compartment, such as regulating dendritic spine morphology; however, no study has evaluated whether and how CYFIP2 affects presynaptic functions. To address this issue, in this study, we have focused on the presynapses of layer 5 neurons of the medial prefrontal cortex (mPFC) in adult Cyfip2 heterozygous (Cyfip2 /?) mice. Electrophysiological analyses revealed an enhancement in the presynaptic short-term plasticity induced by high-frequency stimuli in Cyfip2 /? neurons compared with wild-type neurons. Since presynaptic mitochondria play an important role in buffering presynaptic Ca2 , which is directly associated with the short-term plasticity, we analyzed presynaptic mitochondria using electron microscopic images of the mPFC. Compared with wild-type mice, the number, but not the volume or cristae density, of mitochondria in both presynaptic boutons and axonal processes in the mPFC layer 5 of Cyfip2 /? mice was reduced. Consistent with an identification of mitochondrial proteins in a previously established CYFIP2 interactome, CYFIP2 was detected in a biochemically enriched mitochondrial fraction of the mouse mPFC. Collectively, these results suggest roles for CYFIP2 in regulating presynaptic functions, which may involve presynaptic mitochondrial changes.
机译:细胞质FMR1 - 相互作用蛋白(CYFIP)基因家族,CYFIP1和CYFIP2的变体与许多神经发育和神经精神疾病有关。根据几项研究,Cyfip1调节神经元中突触前和突触后的发育和功能。此外,各种研究评估了在突触后隔室中的CYFIP2功能,例如调节树突脊柱形态;但是,没有研究评估了Cyfip2如何影响突触前功能。为了解决这个问题,在本研究中,我们专注于成人Cyfip2杂合(Cyfip2 /β)小鼠中内侧前额叶皮质(MPFC)的第5层神经元的预突发。电生理学分析揭示了Cyfip2中高频刺激诱导的突触前短期可塑性的增强/?神经元与野生型神经元相比。由于突触前线粒体在缓冲突触前的CA2中发挥着重要作用,其与短期可塑性直接相关,我们使用MPFC的电子显微图像分析了突触前线粒体。与野生型小鼠相比,在Cyfip2的MPFC层5中的突触前Butons和轴突过程中的线粒体的数量,但不是体积或嵴密度。小鼠减少了。与先前建立的Cyfip2酰蛋白组中的线粒体蛋白质的鉴定一致,在小鼠MPFC的生物化学富集的线粒体部分中检测Cyfip2。总的来说,这些结果表明CYFIP2在调节突触前功能方面的作用,这可能涉及突触前线粒体变化。

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