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温度控制的重复热刺激处理的PC12细胞中神经突生长的诱导

Induction of neurite outgrowth in PC12 cells treated with temperature-controlled repeated thermal stimulation.

作者信息

Kudo Tada-aki, Kanetaka Hiroyasu, Mochizuki Kentaro, Tominami Kanako, Nunome Shoko, Abe Genji, Kosukegawa Hiroyuki, Abe Toshihiko, Mori Hitoshi, Mori Kazumi, Takagi Toshiyuki, Izumi Shin-ichi

机构信息

Division of Oral Physiology, Tohoku University Graduate School of Dentistry, Sendai city, Miyagi, Japan.

Liaison Center for Innovative Dentistry, Tohoku University Graduate School of Dentistry, Sendai city, Miyagi, Japan; Tohoku University Graduate School of Biomedical Engineering, Sendai city, Miyagi, Japan.

出版信息

PLoS One. 2015 Apr 16;10(4):e0124024. doi: 10.1371/journal.pone.0124024. eCollection 2015.

Abstract

To promote the functional restoration of the nervous system following injury, it is necessary to provide optimal extracellular signals that can induce neuronal regenerative activities, particularly neurite formation. This study aimed to examine the regulation of neuritogenesis by temperature-controlled repeated thermal stimulation (TRTS) in rat PC12 pheochromocytoma cells, which can be induced by neurotrophic factors to differentiate into neuron-like cells with elongated neurites. A heating plate was used to apply thermal stimulation, and the correlation of culture medium temperature with varying surface temperature of the heating plate was monitored. Plated PC12 cells were exposed to TRTS at two different temperatures via heating plate (preset surface temperature of the heating plate, 39.5°C or 42°C) in growth or differentiating medium for up to 18 h per day. We then measured the extent of growth, neuritogenesis, or acetylcholine esterase (AChE) activity (a neuronal marker). To analyze the mechanisms underlying the effects of TRTS on these cells, we examined changes in intracellular signaling using the following: tropomyosin-related kinase A inhibitor GW441756; p38 mitogen-activated protein kinase (MAPK) inhibitor SB203580; and MAPK/extracellular signal-regulated kinase (ERK) kinase (MEK) inhibitor U0126 with its inactive analog, U0124, as a control. While a TRTS of 39.5°C did not decrease the growth rate of cells in the cell growth assay, it did increase the number of neurite-bearing PC12 cells and AChE activity without the addition of other neuritogenesis inducers. Furthermore, U0126, and SB203580, but not U0124 and GW441756, considerably inhibited TRTS-induced neuritogenesis. These results suggest that TRTS can induce neuritogenesis and that participation of both the ERK1/2 and p38 MAPK signaling pathways is required for TRTS-dependent neuritogenesis in PC12 cells. Thus, TRTS may be an effective technique for regenerative neuromedicine.

摘要

为促进损伤后神经系统的功能恢复,有必要提供能够诱导神经元再生活动,特别是神经突形成的最佳细胞外信号。本研究旨在检测温度控制的重复热刺激(TRTS)对大鼠PC12嗜铬细胞瘤细胞神经突生成的调节作用,该细胞可被神经营养因子诱导分化为具有伸长神经突的神经元样细胞。使用加热板施加热刺激,并监测培养基温度与加热板不同表面温度的相关性。接种的PC12细胞在生长或分化培养基中,通过加热板在两个不同温度下接受TRTS(加热板预设表面温度为39.5°C或42°C),每天长达18小时。然后我们测量了生长、神经突生成或乙酰胆碱酯酶(AChE)活性(一种神经元标志物)的程度。为了分析TRTS对这些细胞作用的潜在机制,我们使用以下方法检测细胞内信号转导的变化:原肌球蛋白相关激酶A抑制剂GW441756;p38丝裂原活化蛋白激酶(MAPK)抑制剂SB203580;以及MAPK/细胞外信号调节激酶(ERK)激酶(MEK)抑制剂U0126及其无活性类似物U0124作为对照。虽然在细胞生长试验中39.5°C的TRTS没有降低细胞的生长速率,但在不添加其他神经突生成诱导剂的情况下,它确实增加了有神经突的PC12细胞数量和AChE活性。此外,U0126和SB203580,但不是U0124和GW441756,显著抑制了TRTS诱导的神经突生成。这些结果表明,TRTS可以诱导神经突生成,并且ERK1/2和p38 MAPK信号通路的参与对于PC12细胞中TRTS依赖的神经突生成是必需的。因此,TRTS可能是一种有效的再生神经医学技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc0b/4399938/6c9ef98e4669/pone.0124024.g006.jpg

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