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短暂且多样的兴奋性毒性损伤会导致新生大脑中神经元核膜通透性增加。

Brief and diverse excitotoxic insults cause an increase in neuronal nuclear membrane permeability in the neonatal brain.

作者信息

Suryavanshi P, Langton R, Fairhead K, Glykys J

机构信息

Department of Pediatrics, University of Iowa, Iowa City, IA.

Iowa Neuroscience Institute, University of Iowa, Iowa City, IA.

出版信息

bioRxiv. 2024 Jan 25:2023.08.22.554167. doi: 10.1101/2023.08.22.554167.

DOI:10.1101/2023.08.22.554167
PMID:37662276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10473591/
Abstract

Neuronal swelling after excitotoxic insults is implicated in neuronal injury and death in the developing brain, yet mitigating brain edema with osmotic and surgical interventions yields poor clinical outcomes. Importantly, neuronal swelling and its downstream consequences during early brain development remain poorly investigated. Using multiphoton Ca imaging (P12-17) and in acute brain slices (P8-12), we explored Ca-dependent downstream effects after neuronal cytotoxic edema. We observed the translocation of cytosolic GCaMP6s into the nucleus of a subpopulation of neurons minutes after various excitotoxic insults. We used automated morphology-detection algorithms for neuronal segmentation and quantified the nuclear translocation of GCaMP6s as the ratio of nuclear and cytosolic intensity (N/C ratio). Elevated neuronal N/C ratios were correlated to higher Ca loads and could occur independently of neuronal swelling. Electron microscopy revealed that the nuclear translocation was associated with increased nuclear pore size. Inhibiting calpains prevented elevated N/C ratios and neuronal swelling. Thus, our results indicate altered nuclear transport in a subpopulation of neurons shortly after injury in the developing brain, which can be used as an early biomarker of acute neuronal injury.

摘要

兴奋性毒性损伤后的神经元肿胀与发育中大脑的神经元损伤和死亡有关,但通过渗透和手术干预减轻脑水肿的临床效果不佳。重要的是,早期脑发育过程中的神经元肿胀及其下游后果仍未得到充分研究。利用多光子钙成像(出生后第12 - 17天)和急性脑片(出生后第8 - 12天),我们探究了神经元细胞毒性水肿后钙依赖性的下游效应。在各种兴奋性毒性损伤后数分钟,我们观察到胞质中的GCaMP6s转位至神经元亚群的细胞核中。我们使用自动形态检测算法对神经元进行分割,并将GCaMP6s的核转位量化为核与胞质强度之比(N/C比)。升高的神经元N/C比与更高的钙负荷相关,并且可能独立于神经元肿胀而发生。电子显微镜显示核转位与核孔大小增加有关。抑制钙蛋白酶可防止N/C比升高和神经元肿胀。因此,我们的结果表明,发育中大脑损伤后不久,神经元亚群中的核转运发生改变,这可用作急性神经元损伤的早期生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/b69e8ce66579/nihpp-2023.08.22.554167v2-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/d3fb6a849aae/nihpp-2023.08.22.554167v2-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/d321bab589a6/nihpp-2023.08.22.554167v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/5f6a2c2e2a13/nihpp-2023.08.22.554167v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/d7da42c6f855/nihpp-2023.08.22.554167v2-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/fea55fa251e3/nihpp-2023.08.22.554167v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/39f55f7e89b9/nihpp-2023.08.22.554167v2-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/b69e8ce66579/nihpp-2023.08.22.554167v2-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/d3fb6a849aae/nihpp-2023.08.22.554167v2-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/d321bab589a6/nihpp-2023.08.22.554167v2-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/5f6a2c2e2a13/nihpp-2023.08.22.554167v2-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/d7da42c6f855/nihpp-2023.08.22.554167v2-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/fea55fa251e3/nihpp-2023.08.22.554167v2-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/39f55f7e89b9/nihpp-2023.08.22.554167v2-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6258/10833741/b69e8ce66579/nihpp-2023.08.22.554167v2-f0007.jpg

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