Fitz J Gregory
UT Southwestern Medical Center, Dallas, TX 75390, USA.
Trans Am Clin Climatol Assoc. 2007;118:199-208.
Epithelial cells exhibit regulated release of ATP. Once outside of the cell, ATP in nanomolar concentrations functions as an autocrine/paracrine signal modulating a broad range of cell and organ functions through activation of purinergic receptors in the plasma membrane. The mechanisms responsible for ATP release have not been defined. In liver cells, there is evidence for ATP translocation through a conductive, channel-mediated pathway. In addition, indirect observations support a second potential mechanism involving exocytosis of ATP-enriched vesicles. Notably, stimuli that increase ATP release are associated with a five- to ten-fold increase in the rate of exocytosis; and inhibition of the exocytic response impairs cellular ATP release. More recent evidence suggests that these vesicles can be visualized, supporting the concept that in liver cells, ATP release is mediated in part by exocytosis of a pool of vesicles enriched in ATP, which can be mobilized within seconds in response to changing physiologic demands.
上皮细胞表现出ATP的调节性释放。一旦ATP释放到细胞外,纳摩尔浓度的ATP作为自分泌/旁分泌信号,通过激活质膜中的嘌呤能受体来调节广泛的细胞和器官功能。负责ATP释放的机制尚未明确。在肝细胞中,有证据表明ATP通过一种传导性的、通道介导的途径进行转运。此外,间接观察结果支持另一种潜在机制,即涉及富含ATP的囊泡的胞吐作用。值得注意的是,增加ATP释放的刺激与胞吐速率增加五到十倍相关;抑制胞吐反应会损害细胞ATP释放。最近的证据表明这些囊泡是可以可视化的,这支持了在肝细胞中,ATP释放部分是由富含ATP的囊泡池的胞吐作用介导的这一概念,这些囊泡可以在几秒钟内响应生理需求的变化而被调动起来。