Hyrc K, Handran S D, Rothman S M, Goldberg M P
Center for the Study of Nervous System Injury, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Neurosci. 1997 Sep 1;17(17):6669-77. doi: 10.1523/JNEUROSCI.17-17-06669.1997.
Cytosolic calcium ([Ca2+]i) is an important mediator of neuronal signal transduction, participating in diverse biochemical reactions that elicit changes in synaptic efficacy, metabolic rate, and gene transcription. Excessive [Ca2+]i also has been implicated as a cause of acute neuronal injury, although measurement of [Ca2+]i in living neurons by fluorescent calcium indicators has not consistently demonstrated a correlation between [Ca2+]i and the likelihood of neuronal death after a variety of potentially lethal insults. Using fluorescence videomicroscopy and microinjected calcium indicators, we measured [Ca2+]i in cultured cortical neurons during intense activation with either NMDA (300 microM) or AMPA (450 microM). At these concentrations NMDA killed >80% of the cultured neurons by the next day, whereas neuronal death from AMPA was <20%. Using the conventional calcium indicator, fura-2/AM, we estimated [Ca2+]i elevations to be approximately 300-400 nM during exposure to either glutamate agonist. In contrast, indicators with lower affinity for calcium, benzothiazole coumarin (BTC), and fura-2/dextran reported [Ca2+]i levels >5 microM during lethal NMDA exposure, but [Ca2+]i levels were <1.5 microM during nonlethal activation of AMPA receptors or voltage-gated calcium channels. Fura-2 reported [Ca2+]i responses during brief exposure to glutamate, NMDA, AMPA, kainate, and elevated extracellular K+ between 0.5 and 1 microM. With the use of BTC, only NMDA and glutamate exposures resulted in micromolar [Ca2+]i levels. Neurotoxic glutamate receptor activation is associated with sustained, micromolar [Ca2+]i elevation. The widely used calcium indicator fura-2 selectively underestimates [Ca2+]i, depending on the route of entry, even at levels that appear to be within its range of detection.
胞浆钙([Ca2+]i)是神经元信号转导的重要介质,参与多种生化反应,引发突触效能、代谢率和基因转录的变化。尽管用荧光钙指示剂测量活神经元中的[Ca2+]i并未始终证明在各种潜在致死性损伤后[Ca2+]i与神经元死亡可能性之间存在相关性,但过量的[Ca2+]i也被认为是急性神经元损伤的一个原因。我们使用荧光视频显微镜和微注射钙指示剂,在培养的皮层神经元用N-甲基-D-天冬氨酸(NMDA,300微摩尔)或α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA,450微摩尔)强烈激活期间测量[Ca2+]i。在这些浓度下,到第二天NMDA杀死了>80%的培养神经元,而AMPA导致的神经元死亡<20%。使用传统的钙指示剂fura-2/AM,我们估计在暴露于任何一种谷氨酸激动剂期间[Ca2+]i升高约为300 - 400纳摩尔。相比之下,对钙亲和力较低的指示剂苯并噻唑香豆素(BTC)和fura-2/葡聚糖报告在致死性NMDA暴露期间[Ca2+]i水平>5微摩尔,但在AMPA受体或电压门控钙通道的非致死性激活期间[Ca2+]i水平<1.5微摩尔。fura-2报告在短暂暴露于谷氨酸、NMDA、AMPA、海人藻酸以及细胞外钾离子在0.5至1微摩尔之间升高时的[Ca2+]i反应。使用BTC时,只有NMDA和谷氨酸暴露导致微摩尔级的[Ca2+]i水平。神经毒性谷氨酸受体激活与持续的微摩尔级[Ca2+]i升高有关。广泛使用的钙指示剂fura-2会选择性地低估[Ca2+]i,这取决于进入途径,即使在看似在其检测范围内的水平也是如此。