Silva Amelia M, Liu-Gentry June, Dickey Adam S, Barnett David W, Misler Stanley
Department of Internal Medicine, Washington University Medical Center, St Louis, MO 63110, USA.
J Physiol. 2005 Jun 15;565(Pt 3):783-99. doi: 10.1113/jphysiol.2005.082586. Epub 2005 Mar 10.
alpha-Latrotoxin (alpha-LT), a potent excitatory neurotoxin, increases spontaneous, as well as action potential-evoked, quantal release at nerve terminals and increases hormone release from excitable endocrine cells. We have investigated the effects of alpha-LT on single human, mouse and canine beta-cells. In isolated and combined measurements, alpha-LT, at nanomolar concentrations, induces: (i) rises in cytosolic Ca(2+), into the micromolar range, that are dependent on extracellular Ca(2+); (ii) large conductance non-selective cation channels; and (iii) Ca(2+)-dependent insulin granule exocytosis, measured as increases in membrane capacitance and quantal release of preloaded serotonin. Furthermore, at picomolar concentrations, alpha-LT potentiates depolarization-induced exocytosis often without evidence of inducing channel activity or increasing cytosolic Ca(2+). These results strongly support the hypothesis that alpha-LT, after binding to specific receptors, has at least two complementary modes of action on excitable cells. (i) alpha-LT inserts into the plasma membrane to form Ca(2+) permeable channels and promote Ca(2+) entry thereby triggering Ca(2+)-dependent exocytosis in unstimulated cells. (ii) At lower concentrations, where its channel forming activity is hardly evident, alpha-LT augments depolarization-evoked exocytosis probably by second messenger-induced enhancement of the efficiency of the vesicle recruitment or vesicle fusion machinery. We suggest that both modes of action enhance exocytosis from a newly described highly Ca(2+)-sensitive pool of insulin granules activated by global cytosolic Ca(2+) concentrations in the range of approximately 1 microm.
α-拉曲毒素(α-LT)是一种强效兴奋性神经毒素,可增加神经末梢的自发性量子释放以及动作电位诱发的量子释放,并增加可兴奋内分泌细胞的激素释放。我们研究了α-LT对单个人类、小鼠和犬β细胞的影响。在单独和联合测量中,纳摩尔浓度的α-LT可诱导:(i)胞质Ca²⁺升高至微摩尔范围,这依赖于细胞外Ca²⁺;(ii)大电导非选择性阳离子通道;以及(iii)Ca²⁺依赖性胰岛素颗粒胞吐作用,通过膜电容增加和预加载血清素的量子释放来衡量。此外,在皮摩尔浓度下,α-LT可增强去极化诱导的胞吐作用,通常没有诱导通道活性或增加胞质Ca²⁺的证据。这些结果有力地支持了以下假设:α-LT与特定受体结合后,对可兴奋细胞至少有两种互补的作用方式。(i)α-LT插入质膜形成Ca²⁺可渗透通道并促进Ca²⁺内流,从而在未受刺激的细胞中触发Ca²⁺依赖性胞吐作用。(ii)在较低浓度下,其通道形成活性几乎不明显,α-LT可能通过第二信使诱导的囊泡募集或囊泡融合机制效率增强来增强去极化诱发的胞吐作用。我们认为这两种作用方式均增强了来自新描述的高度Ca²⁺敏感的胰岛素颗粒池的胞吐作用,该池由约1微摩尔范围内的全局胞质Ca²⁺浓度激活。