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神经生长因子刺激PC12细胞摄取钙:通道的独特性及磷酸化证据

Nerve growth factor-stimulated calcium uptake into PC12 cells: uniqueness of the channel and evidence for phosphorylation.

作者信息

Nikodijevic B, Guroff G

机构信息

Section on Growth Factors, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

出版信息

J Neurosci Res. 1992 Apr;31(4):591-9. doi: 10.1002/jnr.490310402.

Abstract

Nerve growth factor stimulates the uptake of radioactive calcium into PC12 cells. This stimulation is inhibited by low concentrations of dideoxyforskolin or staurosporine, and by high concentrations of nifedipine or cadmium. On the other hand, neither dideoxyforskolin nor staurosporine inhibited the stimulation of calcium uptake caused by BK-8644 or adenosine triphosphate (ATP). Nickel inhibited only the effect of ATP on calcium uptake, and actually stimulated the effects of either BK-8644 or nerve growth factor. Down-regulation of L-calcium channels by BK-8644 blocked the subsequent stimulation of calcium uptake by this agent, but not the stimulation by nerve growth factor. Conversely, pre-treatment of the cells with nerve growth factor inhibited the subsequent stimulation of calcium uptake by nerve growth factor, but not the stimulation by BK-8644. The effects of BK-8644 and nerve growth factor on calcium uptake were additive, as were the effects of nerve growth factor and ATP. Phosphatase 2A inhibited the effect of nerve growth factor on calcium uptake, but did not influence the action of BK-8644. On the other hand, calcineurin inhibited the effect of BK-8644 on calcium uptake, but potentiated the action of nerve growth factor. Calmidazolium or fluphenazine also inhibited the effect of nerve growth factor on calcium uptake, but okadaic acid stimulated it. A comparison of the effects of these inhibitors on the actions of various calcium channel agonists shows that the channels on which the action of nerve growth factor is exerted are different than either the L-type calcium channels or the ATP-activated calcium channels.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

神经生长因子刺激放射性钙进入PC12细胞。低浓度的双脱氧福司可林或星形孢菌素,以及高浓度的硝苯地平或镉可抑制这种刺激。另一方面,双脱氧福司可林和星形孢菌素均未抑制BK - 8644或三磷酸腺苷(ATP)引起的钙摄取刺激。镍仅抑制ATP对钙摄取的作用,实际上还刺激了BK - 8644或神经生长因子的作用。BK - 8644对L - 钙通道的下调阻断了该试剂随后对钙摄取的刺激,但未阻断神经生长因子的刺激。相反,用神经生长因子预处理细胞可抑制随后神经生长因子对钙摄取的刺激,但不抑制BK - 8644的刺激。BK - 8644和神经生长因子对钙摄取的作用是相加的,神经生长因子和ATP的作用也是如此。磷酸酶2A抑制神经生长因子对钙摄取的作用,但不影响BK - 8644的作用。另一方面,钙调神经磷酸酶抑制BK - 8644对钙摄取的作用,但增强神经生长因子的作用。氯氮卓或氟奋乃静也抑制神经生长因子对钙摄取的作用,但冈田酸则刺激该作用。比较这些抑制剂对各种钙通道激动剂作用的影响表明,神经生长因子作用所涉及的通道与L型钙通道或ATP激活的钙通道均不同。(摘要截短至250字)

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