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电刺激培养的海马神经元中的线粒体钙波。

Mitochondrial Calcium Waves by Electrical Stimulation in Cultured Hippocampal Neurons.

机构信息

College of Pharmacy, Chung-Ang University, Seoul, 06974, Republic of Korea.

Brain Research Core Facilities of Korea Brain Research Institute (KBRI), Daegu, 41068, Republic of Korea.

出版信息

Mol Neurobiol. 2024 Jun;61(6):3477-3489. doi: 10.1007/s12035-023-03795-w. Epub 2023 Nov 23.

DOI:10.1007/s12035-023-03795-w
PMID:37995079
Abstract

Mitochondria are critical to cellular Ca homeostasis via the sequestering of cytosolic Ca in the mitochondrial matrix. Mitochondrial Ca buffering regulates neuronal activity and neuronal death by shaping cytosolic and presynaptic Ca or controlling energy metabolism. Dysfunction in mitochondrial Ca buffering has been implicated in psychological and neurological disorders. Ca wave propagation refers to the spreading of Ca for buffering and maintaining the associated rise in Ca concentration. We investigated mitochondrial Ca waves in hippocampal neurons using genetically encoded Ca indicators. Neurons transfected with mito-GCaMP5G, mito-RCaMP1h, and CEPIA3mt exhibited evidence of mitochondrial Ca waves with electrical stimulation. These waves were observed with 200 action potentials at 40 Hz or 20 Hz but not with lower frequencies or fewer action potentials. The application of inhibitors of mitochondrial calcium uniporter and oxidative phosphorylation suppressed mitochondrial Ca waves. However, α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors and N-methyl-d-aspartate receptor blockade had no effect on mitochondrial Ca wave were propagation. The Ca waves were not observed in endoplasmic reticula, presynaptic terminals, or cytosol in association with electrical stimulation of 200 action potentials at 40 Hz. These results offer novel insights into the mechanisms underlying mitochondrial Ca buffering and the molecular basis of mitochondrial Ca waves in neurons in response to electrical stimulation.

摘要

线粒体通过将细胞质中的 Ca 离子隔离在基质中来维持细胞内 Ca 离子的平衡。线粒体 Ca 缓冲作用通过调节细胞质和突触前 Ca 离子或控制能量代谢来调节神经元的活性和神经元的死亡。线粒体 Ca 缓冲功能障碍与心理和神经紊乱有关。Ca 波传播是指 Ca 离子的扩散,用于缓冲和维持相关的 Ca 离子浓度升高。我们使用基因编码的 Ca 指示剂研究了海马神经元中的线粒体 Ca 波。用 mito-GCaMP5G、mito-RCaMP1h 和 CEPIA3mt 转染的神经元在电刺激下表现出线粒体 Ca 波的证据。这些波在 40 Hz 或 20 Hz 的 200 个动作电位刺激下观察到,但在较低频率或较少动作电位刺激下观察不到。线粒体钙单向转运体和氧化磷酸化抑制剂的应用抑制了线粒体 Ca 波的传播。然而,α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体和 N-甲基-D-天冬氨酸受体阻断剂对线粒体 Ca 波的传播没有影响。在 40 Hz 的 200 个动作电位电刺激下,Ca 波在与内质网、突触前末端或细胞质相关的情况下没有被观察到。这些结果为理解线粒体 Ca 缓冲作用的机制以及神经元对电刺激的线粒体 Ca 波的分子基础提供了新的见解。

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本文引用的文献

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MCU-induced mitochondrial calcium uptake promotes mitochondrial biogenesis and colorectal cancer growth.MCU 诱导的线粒体钙摄取促进了线粒体生物发生和结直肠癌细胞生长。
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