Pothos Emmanuel N, Mosharov Eugene, Liu Kuo-Peing, Setlik Wanda, Haburcak Marian, Baldini Giulia, Gershon Michael D, Tamir Hadassah, Sulzer David
Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, Boston, MA 0211, USA.
J Physiol. 2002 Jul 15;542(Pt 2):453-76. doi: 10.1113/jphysiol.2002.018630.
Trapping of weak bases was utilized to evaluate stimulus-induced changes in the internal pH of the secretory vesicles of chromaffin cells and enteric neurons. The internal acidity of chromaffin vesicles was increased by the nicotinic agonist 1,1-dimethyl-4-phenyl-piperazinium iodide (DMPP; in vivo and in vitro) and by high K+ (in vitro); and in enteric nerve terminals by exposure to veratridine or a plasmalemmal [Ca2+]o receptor agonist (Gd3+). Stimulation-induced acidification of chromaffin vesicles was [Ca2+]o-dependent and blocked by agents that inhibit the vacuolar proton pump (vH+-ATPase) or flux through Cl- channels. Stimulation also increased the average volume of chromaffin vesicles and the proportion that displayed a clear halo around their dense cores (called active vesicles). Stimulation-induced increases in internal acidity and size were greatest in active vesicles. Stimulation of chromaffin cells in the presence of a plasma membrane marker revealed that membrane was internalized in endosomes but not in chromaffin vesicles. The stable expression of botulinum toxin E to prevent exocytosis did not affect the stimulation-induced acidification of the secretory vesicles of mouse neuroblastoma Neuro2A cells. Stimulation-induced acidification thus occurs independently of exocytosis. The quantal size of secreted catecholamines, measured by amperometry in cultured chromaffin cells, was found to be increased either by prior exposure to L-DOPA or stimulation by high K+, and decreased by inhibition of vH+-ATPase or flux through Cl- channels. These observations are consistent with the hypothesis that the content of releasable small molecules in secretory vesicles is increased when the driving force for their uptake is enhanced, either by increasing the transmembrane concentration or pH gradients.
利用弱碱捕获法评估刺激引起的嗜铬细胞和肠神经元分泌囊泡内pH值的变化。烟碱激动剂1,1 - 二甲基 - 4 - 苯基 - 哌嗪碘化物(DMPP;体内和体外)以及高钾(体外)可增加嗜铬囊泡的内部酸度;在肠神经末梢,暴露于藜芦碱或质膜[Ca2+]o受体激动剂(Gd3+)也可增加其内部酸度。刺激诱导的嗜铬囊泡酸化依赖于[Ca2+]o,并被抑制液泡质子泵(vH+-ATPase)或通过Cl-通道的通量的试剂所阻断。刺激还增加了嗜铬囊泡的平均体积以及在其致密核心周围显示清晰晕圈的囊泡比例(称为活性囊泡)。活性囊泡中刺激诱导的内部酸度和大小增加最为显著。在存在质膜标记物的情况下刺激嗜铬细胞发现,膜被内化到内体中,而不是嗜铬囊泡中。肉毒杆菌毒素E的稳定表达以防止胞吐作用并不影响刺激诱导的小鼠神经母细胞瘤Neuro2A细胞分泌囊泡的酸化。因此,刺激诱导的酸化独立于胞吐作用发生。通过安培法在培养的嗜铬细胞中测量的分泌儿茶酚胺的量子大小,发现要么通过预先暴露于L - DOPA或高钾刺激而增加,要么通过抑制vH+-ATPase或通过Cl-通道的通量而降低。这些观察结果与以下假设一致:当通过增加跨膜浓度或pH梯度来增强分泌囊泡中可释放小分子摄取的驱动力时,其含量会增加。