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凝血酶和钙在人脐静脉培养的单个内皮细胞中诱导的膜电容变化。

Membrane capacitance changes induced by thrombin and calcium in single endothelial cells cultured from human umbilical vein.

作者信息

Carter T D, Zupancic G, Smith S M, Wheeler-Jones C, Ogden D

机构信息

National Institute for Medical Research, Mill Hill, London NW7 1AA,,

出版信息

J Physiol. 1998 Dec 15;513 ( Pt 3)(Pt 3):845-55. doi: 10.1111/j.1469-7793.1998.845ba.x.

Abstract
  1. Vesicular secretion from single human umbilical vein endothelial cells (HUVECs) was monitored by changes in membrane capacitance (Cm). Secretion was evoked by dialysis with strongly buffered intracellular free Ca2+ concentrations ([Ca2+]i), flash photolysis of Ca2+-loaded DM-nitrophen or caged InsP3, or by thrombin. [Ca2+]i was monitored spectrofluorimetrically with furaptra. The results show that a large, slowly rising component of vesicular secretion requires prolonged exposure to high [Ca2+]i. 2. Cm increased during intracellular perfusion with [Ca2+] buffered in the range 1.0-20 microM. Changes in Cm comprised an initial slowly rising small component of 0.1-0.5 pF followed by a faster rising larger component of up to approximately 7 pF, seen when [Ca2+]i > 2 microM and which was maximal at 10-20 microM Ca2+. 3. Thrombin evoked rapid initial elevations of [Ca2+]i to a peak of 7.1 +/- 1.5 microM (mean +/- s.e. m., n = 5) that declined within approximately 20-30 s with thrombin present either to resting levels or to a maintained elevated level of 2.0 +/- 0.7 microM (mean +/- s.e.m., range 1.0-3.6 microM, n = 3). Transient [Ca2+]i rises were associated with small, slowly rising increases in Cm of 0.1-0.2 pF, that recovered to pre-application levels over 2-3 min. Maintained elevations of [Ca2+]i caused larger, faster-rising sustained increases in Cm to 1.14 +/- 0.12 pF (mean +/- s.e.m., n = 3). Separate specific enzyme-linked immunosorbent assay (ELISA) showed that 1.0 U ml-1 thrombin produced secretion of von Willebrand factor in HUVEC cultures. 4. Short-lived [Ca2+]i elevations with a peak of 3-25 microM and a duration of approximately 20 s generated by flash photolysis of caged InsP3 or DM-nitrophen produced either no net change in Cm, or small slow increases of approximately 0.1-0.6 pF at up to 5 fF s-1 that recovered to pre-flash levels over 2-3 min. 5. Maintained elevations of [Ca2+]i in the range 1-28 microM produced by flash photolysis of DM-nitrophen caused large increases in Cm, up to approximately 4 pF, corresponding to approximately 25-30 % of the initial cell Cm. The maximum rate of change of Cm was up to 50 fF s-1 at steady [Ca2+] up to 20 microM; Cm recovered towards pre-flash levels only when [Ca2+] had declined.
摘要
  1. 通过膜电容(Cm)的变化监测单个脐静脉内皮细胞(HUVEC)的囊泡分泌。用强缓冲的细胞内游离钙离子浓度([Ca2+]i)进行透析、对负载钙离子的DM-硝基苯酚或笼化肌醇三磷酸(InsP3)进行闪光光解,或用凝血酶刺激来引发分泌。用氟甲喹分光荧光法监测[Ca2+]i。结果表明,囊泡分泌的一个大的、缓慢上升的成分需要长时间暴露于高[Ca2+]i。2. 在用1.0 - 20微摩尔缓冲的[Ca2+]进行细胞内灌注期间,Cm增加。Cm的变化包括一个初始缓慢上升的小成分,为0.1 - 0.5皮法,随后是一个上升更快的大成分,可达约7皮法,当[Ca2+]i > 2微摩尔时出现,在10 - 20微摩尔钙离子时达到最大。3. 凝血酶引起[Ca2+]i迅速初始升高至峰值7.1±1.5微摩尔(平均值±标准误,n = 5),在有凝血酶存在的情况下,约20 - 30秒内下降至静息水平或维持在2.0±0.7微摩尔的升高水平(平均值±标准误,范围1.0 - 3.6微摩尔,n = 3)。短暂的[Ca2+]i升高与Cm缓慢上升的小增加相关,为0.1 - 0.2皮法,在2 - 3分钟内恢复到应用前水平。[Ca2+]i的持续升高导致Cm更大、上升更快的持续增加,达到1.14±0.12皮法(平均值±标准误,n = 3)。单独的特异性酶联免疫吸附测定(ELISA)表明,1.0 U/ml凝血酶在HUVEC培养物中产生血管性血友病因子的分泌。4. 通过对笼化InsP3或DM-硝基苯酚进行闪光光解产生的峰值为3 - 25微摩尔、持续时间约20秒的短暂[Ca2+]i升高,要么使Cm无净变化,要么以高达5飞法/秒的速度缓慢增加约0.1 - 0.6皮法,并在2 - 3分钟内恢复到闪光前水平。5. 通过对DM-硝基苯酚进行闪光光解在1 - 28微摩尔范围内产生的[Ca2+]i持续升高导致Cm大幅增加,可达约4皮法,相当于初始细胞Cm的约25 - 30%。在稳定[Ca2+]高达20微摩尔时,Cm的最大变化率高达50飞法/秒;只有当[Ca2+]下降时,Cm才恢复到闪光前水平。

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