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The RNA-binding protein RBM3 is involved in hypothermia induced neuroprotection

机译:RNA结合蛋白RBM3参与低温诱导的神经保护

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摘要

Induced hypothermia is the only therapy with proven efficacy to reduce brain damage after perinatal asphyxia. While hypothermia down-regulates global protein synthesis and cell metabolism, low temperature induces a small subset of proteins that includes the RNA-binding protein RBM3 (RNA-binding motif protein 3), which has recently been implicated in cell survival. Here, immunohistochemistry of the developing postnatal murine brain revealed a spatio-temporal neuronal RBM3 expression pattern very similar to that of doublecortin, a marker of neuronal precursor cells. Mild hypothermia (32°C) profoundly promoted RBM3 expression and rescued neuronal cells from forced apoptosis as studied in primary neurons, PC12 cells, and cortical organotypic slice cultures. Blocking RBM3 expression in neuronal cells by specific siRNAs significantly diminished the neuroprotective effect of hypothermia while vector-driven RBM3 over-expression reduced cleavage of PARP, prevented internucleosomal DNA fragmentation, and LDH release also in the absence of hypothermia. Together, neuronal RBM3 up-regulation in response to hypothermia apparently accounts for a substantial proportion of hypothermia-induced neuroprotection.
机译:诱导性体温过低是唯一有效的减少围产期窒息后脑损伤的疗法。低温会下调整体蛋白质的合成和细胞代谢,而低温会诱导一小部分蛋白质,其中包括RNA结合蛋白RBM3(RNA结合基序蛋白3),最近该现象与细胞存活有关。在这里,正在发育的产后鼠脑的免疫组织化学揭示了时空神经元RBM3表达模式与双皮质素(神经元前体细胞的标志物)非常相似。如在原代神经元,PC12细胞和皮层器官型切片培养物中所研究的那样,轻度低温(32°C)极大地促进了RBM3表达,并使神经元细胞免于强迫性凋亡。通过特异性siRNA阻止神经元细胞中RBM3的表达,大大降低了体温过低的神经保护作用,而载体驱动的RBM3过表达减少了PARP的裂解,防止了核小体DNA片段化,并且在缺乏体温过低的情况下也释放LDH。总之,对体温过低作出反应的神经元RBM3上调显然占体温过低引起的神经保护作用的主要部分。

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