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由ATP的点源爆发式释放介导的细胞间钙信号传导。

Intercellular calcium signaling mediated by point-source burst release of ATP.

作者信息

Arcuino Gregory, Lin Jane H-C, Takano Takahiro, Liu Collins, Jiang Li, Gao Qun, Kang Jian, Nedergaard Maiken

机构信息

Department of Cell Biology, Anatomy, and Pathology, New York Medical College, Valhalla, NY 10595, USA.

出版信息

Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):9840-5. doi: 10.1073/pnas.152588599. Epub 2002 Jul 3.

Abstract

Calcium signaling, manifested as intercellular waves of rising cytosolic calcium, is, in many cell types, the result of calcium-induced secretion of ATP and activation of purinergic receptors. The mechanism by which ATP is released has hitherto not been established. Here, we show by real-time bioluminescence imaging that ATP efflux is not uniform across a field of cells but is restricted to brief, abrupt point-source bursts. The ATP bursts emanate from single cells and manifest the transient opening of nonselective membrane channels, which admits fluorescent indicators of < or = 1.5 kDa. These observations challenge the existence of regenerative ATP release, because ATP efflux is finite and restricted to a point source. Transient efflux of cytosolic nucleotides from a subset of cells may represent a conserved pathway for coordinating local activity of electrically nonexcitable cells, because identical patterns of ATP release were identified in human astrocytes, endothelial cells, and bronchial epithelial cells.

摘要

钙信号传导表现为胞质钙升高的细胞间波,在许多细胞类型中,是由钙诱导的ATP分泌和嘌呤能受体激活所致。迄今为止,ATP释放的机制尚未明确。在此,我们通过实时生物发光成像显示,ATP外流在细胞群中并不均匀,而是局限于短暂、突然的点源爆发。ATP爆发源自单个细胞,并表现为非选择性膜通道的短暂开放,该通道允许分子量小于或等于1.5 kDa的荧光指示剂通过。这些观察结果对再生性ATP释放的存在提出了质疑,因为ATP外流是有限的且局限于一个点源。来自一部分细胞的胞质核苷酸的短暂外流可能代表了一种保守的途径,用于协调电非兴奋性细胞的局部活动,因为在人星形胶质细胞、内皮细胞和支气管上皮细胞中发现了相同的ATP释放模式。

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