Department of Pharmacology and Physiology, University of Rochester Medical School, Rochester, NY 14642, USA. David
Int J Biochem Cell Biol. 2010 Nov;42(11):1757-61. doi: 10.1016/j.biocel.2010.07.007. Epub 2010 Jul 15.
Pancreatic acinar cells are classical exocrine gland cells. The apical regions of clusters of coupled acinar cells collectively form a lumen which constitutes the blind end of a tube created by ductal cells - a structure reminiscent of a "bunch of grapes". When activated by neural or hormonal secretagogues, pancreatic acinar cells are stimulated to secrete a variety of proteins. These proteins are predominately inactive digestive enzyme precursors called "zymogens". Acinar cell secretion is absolutely dependent on secretagogue-induced increases in intracellular free Ca(2+). The increase in Ca(2+) has precise temporal and spatial characteristics as a result of the exquisite regulation of the proteins responsible for Ca(2+) release, Ca(2+) influx and Ca(2+) clearance in the acinar cell. This brief review discusses recent studies in which transgenic animal models have been utilized to define in molecular detail the components of the Ca(2+) signaling machinery which contribute to these characteristics.
胰腺腺泡细胞是经典的外分泌腺细胞。成群的胰腺腺泡细胞的顶端区域共同形成一个腔,该腔构成由导管细胞形成的管的盲端 - 这种结构让人联想到“一串葡萄”。当被神经或激素分泌激动剂激活时,胰腺腺泡细胞受到刺激分泌各种蛋白质。这些蛋白质主要是无活性的消化酶前体,称为“酶原”。腺泡细胞的分泌绝对依赖于分泌激动剂诱导的细胞内游离 Ca(2+)增加。由于对负责 Ca(2+)释放、Ca(2+)内流和 Ca(2+)清除的蛋白质进行了精细调节,Ca(2+)的增加具有精确的时间和空间特征。这篇简短的综述讨论了最近的研究,其中利用转基因动物模型从分子细节上定义了参与这些特征的 Ca(2+)信号转导机制的组成部分。