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微血管内皮细胞中的异质性细胞质钙反应。

Heterogeneous cytoplasmic calcium response in microvascular endothelial cells.

作者信息

Hong D, Barbee K A, Buerk D G, Jaron D

机构信息

School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, 19104, USA.

出版信息

Conf Proc IEEE Eng Med Biol Soc. 2005;2005:7493-6. doi: 10.1109/IEMBS.2005.1616245.

Abstract

We investigated changes in calcium concentration in response to the administration of ATP and the onset of shear stress with cultured rat adrenomedulary endothelial cells (RAMECs, microvascular). A substantial heterogeneity in time and space in the calcium response was observed. The onset of shear stress induced calcium waves that originated from one or several cells and propagated to neighboring cells The application of uniform exogenous ATP produced similar heterogeneous calcium transients. The size of the responding groups was dependent on ATP concentration. The propagation of calcium waves induced by either ATP or shear stress challenge was significantly suppressed by suramin, a non-specific purinergic receptor blocker. We investigated some of the mechanisms leading to the heterogeneity, and the results indicated that the main source of variation is the heterogeneous distribution of purinergic receptor. The application of ATP or shear stress stimulates cells to release ATP causing an increase of [Ca]ivia purinergic receptor in the cells that have high sensitivity. Subsequently, additional ATP is released and the elevation of ATP concentration in the vicinity of the initially responding cells mediates the calcium propagation. These data suggest a mechanism by which ATP acts as an autocrine and paracrine mediator to integrate individual cell responses that result in coordination of vascular functions in situ.

摘要

我们用培养的大鼠肾上腺髓质内皮细胞(RAMECs,微血管)研究了给予ATP以及开始施加剪切应力后钙浓度的变化。观察到钙反应在时间和空间上存在显著的异质性。剪切应力的开始诱导了钙波,这些钙波起源于一个或几个细胞,并传播到相邻细胞。施加均匀的外源性ATP产生了类似的异质性钙瞬变。反应组的大小取决于ATP浓度。苏拉明(一种非特异性嘌呤能受体阻滞剂)显著抑制了由ATP或剪切应力刺激诱导的钙波传播。我们研究了导致这种异质性的一些机制,结果表明,变异的主要来源是嘌呤能受体的异质分布。ATP或剪切应力的施加刺激细胞释放ATP,通过高敏感性细胞中的嘌呤能受体导致[Ca]i升高。随后,更多的ATP被释放,最初反应细胞附近ATP浓度的升高介导了钙的传播。这些数据提示了一种机制,通过该机制ATP作为自分泌和旁分泌介质,整合个体细胞反应,从而实现局部血管功能的协调。

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