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神经生长因子和v-src癌基因对大鼠嗜铬细胞瘤细胞中钙离子通道表达的增强作用

Enhanced expression of Ca2+ channels by nerve growth factor and the v-src oncogene in rat phaeochromocytoma cells.

作者信息

Lewis D L, De Aizpurua H J, Rausch D M

机构信息

Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta 30912.

出版信息

J Physiol. 1993 Jun;465:325-42. doi: 10.1113/jphysiol.1993.sp019679.

Abstract
  1. Rat phaeochromocytoma (PC12) cells were used to investigate the expression of Ca2+ channel types during neuronal differentiation. Neuronal differentiation was induced by treatment with nerve growth factor (NGF) or by activation of a temperature-sensitive tyrosine kinase (pp60v-src) in genetically modified PC12 (PC12/v-src) cells. PC12 cells differentiated morphologically in the presence of NGF. When grown at the permissive temperature of 37 degrees C which activates the kinase activity of pp60v-src, PC12/v-src cells differentiated morphologically with the extension of neurites. In contrast, PC12/v-src cells grown at the non-permissive temperature of 40 degrees C continued to divide and were morphologically indistinguishable from control PC12 cells. 2. Whole-cell Ca2+ currents were measured in PC12 cells using Ba2+ as the charge carrier. Ba2+ currents measured at the peak of the current-voltage curve from a holding potential of -80 mV were -0.28 +/- 0.04 nA (mean +/- S.E.M.) in control PC12 cells compared to -1.25 +/- 0.16 nA in NGF-differentiated cells. The current density increased from 9.4 +/- 0.7 pA/pF in control PC12 cells to 22.8 +/- 2.4 pA/pF in NGF-differentiated PC12 cells. Ba2+ currents were -0.24 +/- 0.04 nA in undifferentiated PC12/v-src cells grown at the non-permissive temperature of 40 degrees C compared to -0.95 +/- 0.16 nA in differentiated PC12/v-src cells grown at the permissive temperature of 37 degrees C. The current density increased from 4.5 +/- 0.5 pA/pF in PC12/v-src cells grown at the non-permissive temperature of 40 degrees C to 13.3 +/- 2.4 pA/pF in PC12/v-src cells grown at the permissive temperature of 37 degrees C. 3. The sensitivity of Ba2+ currents to omega-conotoxin GVIA (omega-CgTX) was determined for currents measured at the peak of the current-voltage curve (0 mV in 10 mM Ba2+) from a holding potential of -80 mV. In NGF-differentiated PC12 cells, 10 microM omega-CgTx inhibited 68.1 +/- 3.2% of the total Ba2+ current compared to 35.9 +/- 4.1% in control cells. The density of the omega-CgTX-sensitive current increased from 3.3 +/- 0.4 pA/pF in control cells to 15.7 +/- 2.0 pA/pF in NGF-differentiated cells. In differentiated PC12/v-src cells grown at 37 degrees C, omega-CgTX inhibited 52.2 +/- 4.2% of total Ba2+ current compared to 41.1 +/- 3.8% in PC12/v-src cells grown at 40 degrees C. The density of the omega-CgTX-sensitive current increased from 1.9 +/- 0.3 to 7.4 +/- 2.0 pA/pF with v-src-mediated differentiation.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用大鼠嗜铬细胞瘤(PC12)细胞来研究神经元分化过程中钙离子通道类型的表达。通过用神经生长因子(NGF)处理或激活基因改造的PC12(PC12/v-src)细胞中的温度敏感型酪氨酸激酶(pp60v-src)来诱导神经元分化。在NGF存在的情况下,PC12细胞发生形态学分化。当在激活pp60v-src激酶活性的37℃允许温度下培养时,PC12/v-src细胞随着神经突的延伸发生形态学分化。相反,在40℃非允许温度下培养的PC12/v-src细胞继续分裂,并且在形态上与对照PC12细胞无法区分。2. 使用Ba2+作为电荷载体在PC12细胞中测量全细胞Ca2+电流。在对照PC12细胞中,从 -80 mV的保持电位在电流 - 电压曲线峰值处测量的Ba2+电流为 -0.28±0.04 nA(平均值±标准误),而在NGF分化的细胞中为 -1.25±0.16 nA。电流密度从对照PC12细胞中的9.4±0.7 pA/pF增加到NGF分化的PC12细胞中的22.8±2.4 pA/pF。在40℃非允许温度下培养的未分化PC12/v-src细胞中,Ba2+电流为 -0.24±0.04 nA,而在37℃允许温度下培养的分化PC12/v-src细胞中为 -0.95±0.16 nA。电流密度从在40℃非允许温度下培养的PC12/v-src细胞中的4.5±0.5 pA/pF增加到在37℃允许温度下培养的PC12/v-src细胞中的13.3±2.4 pA/pF。3. 对于从 -80 mV的保持电位在电流 - 电压曲线峰值(在10 mM Ba2+中为0 mV)处测量的电流,测定Ba2+电流对ω-芋螺毒素GVIA(ω-CgTX)的敏感性。在NGF分化的PC12细胞中,10μM ω-CgTx抑制了68.1±3.2%的总Ba2+电流,而在对照细胞中为35.9±4.1%。ω-CgTX敏感电流的密度从对照细胞中的3.3±0.4 pA/pF增加到NGF分化细胞中的15.7±2.0 pA/pF。在37℃培养的分化PC12/v-src细胞中,ω-CgTX抑制了52.2±4.2%的总Ba2+电流,而在40℃培养的PC12/v-src细胞中为41.1±3.8%。随着v-src介导的分化,ω-CgTX敏感电流的密度从1.9±0.3增加到7.4±2.0 pA/pF。(摘要截断于400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a90c/1175432/864970e033e5/jphysiol00417-0331-a.jpg

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